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Identification of avaC from Human Gut Microbial Isolates that Converts 5AVA to 2-Piperidone
Qiudi Zhou, Lihui Feng
J. Microbiol. 2024;62(5):367-379.   Published online June 17, 2024
DOI: https://doi.org/10.1007/s12275-024-00141-0
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AbstractAbstract PDF
2-piperidone is a crucial industrial raw material of high-value nylon-5 and nylon-6,5. Currently, a major bottleneck in the biosynthesis of 2-piperidone is the identification of highly efficient 2-piperidone synthases. In this study, we aimed to identify specific strains among 51 human gut bacterial strains capable of producing 2-piperidone and to elucidate its synthetic mechanism. Our findings revealed that four gut bacterial strains, namely Collinsella aerofaciens LFYP39, Collinsella intestinalis LFYP54, Clostridium bolteae LFYP116, and Clostridium hathewayi LFYP18, could produce 2-piperidone from 5-aminovaleric acid (5AVA). Additionally, we observed that 2-piperidone could be synthesized from proline through cross-feeding between Clostridium difficile LFYP43 and one of the four 2-piperidone producing strains, respectively. To identify the enzyme responsible for catalyzing the conversion of 5AVA to 2-piperidone, we utilized a gain-of-function library and identified avaC (5-aminovaleric acid cyclase) in C. intestinalis LFYP54. Moreover, homologous genes of avaC were validated in the other three bacterial strains. Notably, avaC were found to be widely distributed among environmental bacteria. Overall, our research delineated the gut bacterial strains and genes involved in 2-piperidone production, holding promise for enhancing the efficiency of industrial biosynthesis of this compound.

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  • Metabolite biomarkers of screening neonatal congenital hypothyroidism based on dried blood spot metabolomics
    Xingyu Guo, Feng Suo, Yuting Wang, Di Yu, Yi Wang, Bulian Dong, Lingshan Gou, Xinhui Gan, Benjing Wang, Chaowen Yu, Xiaoxiang Xie, Dandan Linghu, Xinyu Liu, Maosheng Gu, Guowang Xu
    Analytical and Bioanalytical Chemistry.2025; 417(13): 2889.     CrossRef
Recombinant Protein Mimicking the Antigenic Structure of the Viral Surface Envelope Protein Reinforces Induction of an Antigen‑Specific and Virus‑Neutralizing Immune Response Against Dengue Virus
Ju Kim , Tae Young Lim , Jisang Park , Yong&#
J. Microbiol. 2023;61(1):131-143.   Published online February 1, 2023
DOI: https://doi.org/10.1007/s12275-023-00021-z
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AbstractAbstract PDF
Dengue virus (DENV), belonging to the family Flaviviridae, is the causative agent of dengue and comprises four serotypes. A second heterologous DENV infection is a critical risk factor for severe dengue, and no effective vaccine is available to prevent infection by all four DENV serotypes. Recombinant DENV vaccines are primarily based on the envelope proteins, prM and E. The E protein and its envelope domain III (EDIII) have been investigated as candidate antigens (Ags) for recombinant subunit vaccines. However, most EDIII-based Ags are monomers that do not display the cognate antigenic structure of E protein, which is essential for induction of virus-neutralizing immunity. Here, we developed recombinant DENV-2 envelope domain (r2ED) protein as an Ag that mimics the quaternary structure of E protein on the DENV surface. We confirmed that r2ED retained the conformational epitope displayed at the E-dimer interface, which reportedly exhibits broad virus-neutralizing capacity, without displaying the fusion loop epitope that causes antibody (Ab)-dependent enhancement. Furthermore, compared with EDIII alone, r2ED elicited stronger Ag-specific and cross-reactive neutralizing Ab and T cell-mediated immune responses in mice. This Ag-specific immunity was maintained at an elevated level 6 months after the last immunization, suggesting sustained Ag-specific immune memory. Taken together, these observations suggest that r2ED could be used to develop an improved subunit vaccine capable of inducing a broadly cross-reactive and long-lasting immune response against DENV infection.

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  • Antiviral effects of heme oxygenase-1 against canine coronavirus and canine influenza virus in vitro
    Jae-Hyeong Kim, Dong-Hwi Kim, Kyu-Beom Lim, Joong-Bok Lee, Seung-Yong Park, Chang-Seon Song, Sang-Won Lee, Dong-Hun Lee, Do-Geun Kim, Hun-Young Yoon, In-Soo Choi
    Journal of Microbiology.2025; 63(5): e2501029.     CrossRef
  • Peptides of a Feather: How Computation Is Taking Peptide Therapeutics under Its Wing
    Thomas David Daniel Kazmirchuk, Calvin Bradbury-Jost, Taylor Ann Withey, Tadesse Gessese, Taha Azad, Bahram Samanfar, Frank Dehne, Ashkan Golshani
    Genes.2023; 14(6): 1194.     CrossRef
Role of melatonin in murine “restraint stress”-induced dysfunction of colonic microbiota
Rutao Lin , Zixu Wang , Jing Cao , Ting Gao , Yulan Dong , Yaoxing Chen
J. Microbiol. 2021;59(5):500-512.   Published online February 25, 2021
DOI: https://doi.org/10.1007/s12275-021-0305-7
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AbstractAbstract PDF
Intestinal diseases caused by physiological stress have become a severe public health threat worldwide. Disturbances in the gut microbiota-host relationship have been associated with irritable bowel disease (IBD), while melatonin (MT) has antiinflammatory and antioxidant effects. The objective of this study was to investigate the mechanisms by which MT-mediated protection mitigated stress-induced intestinal microbiota dysbiosis and inflammation. We successfully established a murine restraint stress model with and without MT supplementation. Mice subjected to restraint stress had significantly elevated corticosterone (CORT) levels, decreased MT levels in their plasma, elevated colonic ROS levels and increased bacterial abundance, including Bacteroides and Tyzzerella, in their colon tract, which led to elevated expression of Toll-like receptor (TLR) 2/4, p-P65 and p-IκB. In contrast, supplementation with 20 mg/kg MT reversed the elevation of the plasma CORT levels, downregulated the colon ROS levels and inhibited the changes in the intestinal microbiota induced by restraint stress. These effects, in turn, inhibited the activities of TLR2 and TLR4, p-P65 and p-IκB, and decreased the inflammatory reaction induced by restraint stress. Our results suggested that MT may mitigate “restraint stress”-induced colonic microbiota dysbiosis and intestinal inflammation by inhibiting the activation of the NF-κB pathway.

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  • Tryptophan Attenuates Chronic Restraint Stress-Induced Intestinal Injury Through Modulation of Intestinal Barrier Integrity and Gut Microbiota Homeostasis
    Jianhua Zheng, Tianqi Sun, Tongtong Qin, Yunpeng Wu, Wensheng Zhang, Yefeng Qiu, Jingqing Chen
    Nutrients.2025; 17(6): 975.     CrossRef
  • Distribution of gut microbiota across intestinal segments and their impact on human physiological and pathological processes
    Ke Yang, Guangqin Li, Qihong Li, Wei Wang, Xu Zhao, Nan Shao, Hui Qiu, Jing Liu, Lin Xu, Juanjuan Zhao
    Cell & Bioscience.2025;[Epub]     CrossRef
  • Microbial melatonin metabolism in the human intestine as a therapeutic target for dysbiosis and rhythm disorders
    Petra Zimmermann, Salome Kurth, Benoit Pugin, Nicholas A. Bokulich
    npj Biofilms and Microbiomes.2024;[Epub]     CrossRef
  • Toll-like receptor 4 plays a vital role in irritable bowel syndrome: a scoping review
    Xuemeng Wan, Liyuan Wang, Zhiling Wang, Chaomin Wan
    Frontiers in Immunology.2024;[Epub]     CrossRef
  • Christensenella minuta mitigates behavioral and cardiometabolic hallmarks of social defeat stress
    A. Agusti, GV. Molina-Mendoza, M. Tamayo, V. Rossini, MC. Cenit, C. Frances-Cuesta, V. Tolosa-Enguis, EM. Gómez Del Pulgar, A. Flor-Duro, Y. Sanz
    Biomedicine & Pharmacotherapy.2024; 180: 117377.     CrossRef
  • The impact of acute and chronic stress on gastrointestinal physiology and function: a microbiota–gut–brain axis perspective
    Sarah‐Jane Leigh, Friederike Uhlig, Lars Wilmes, Paula Sanchez‐Diaz, Cassandra E. Gheorghe, Michael S. Goodson, Nancy Kelley‐Loughnane, Niall P. Hyland, John F. Cryan, Gerard Clarke
    The Journal of Physiology.2023; 601(20): 4491.     CrossRef
  • Melatonin as a Mediator of the Gut Microbiota–Host Interaction: Implications for Health and Disease
    María-Ángeles Bonmatí-Carrión, Maria-Angeles Rol
    Antioxidants.2023; 13(1): 34.     CrossRef
  • INVESTIGATION OF THE ROLE OF STRESS IN MALE INFERTILITY AND THE EFFECT OF CURRENT MELATONIN HORMONE TREATMENTS
    İshak GÖKÇEK, Leyla AYDIN
    Veteriner Farmakoloji ve Toksikoloji Derneği Bülteni.2023; 14(1): 36.     CrossRef
  • The double burden of malnutrition and environmental enteric dysfunction as potential factors affecting gut-derived melatonin in children under adverse environments
    Alane N. Bezerra, Caroline L. Peixoto, Synara C. Lopes, Veralice M. S. Bruin, Pedro Felipe C. Bruin, Reinaldo B. Oriá
    Frontiers in Nutrition.2023;[Epub]     CrossRef
  • Melatonin: Both a Messenger of Darkness and a Participant in the Cellular Actions of Non-Visible Solar Radiation of Near Infrared Light
    Dun-Xian Tan, Russel J. Reiter, Scott Zimmerman, Ruediger Hardeland
    Biology.2023; 12(1): 89.     CrossRef
  • Glucocorticoids coordinate the bladder peripheral clock and diurnal micturition pattern in mice
    Ichiro Chihara, Hiromitsu Negoro, Jin Kono, Yoshiyuki Nagumo, Haruki Tsuchiya, Kosuke Kojo, Masanobu Shiga, Ken Tanaka, Shuya Kandori, Bryan J. Mathis, Hiroyuki Nishiyama
    Communications Biology.2023;[Epub]     CrossRef
  • The Microbiota-Dependent Worsening Effects of Melatonin on Gut Inflammation
    Jefferson Luiz da Silva, Lia Vezenfard Barbosa, Camila Figueiredo Pinzan, Viviani Nardini, Irislene Simões Brigo, Cássia Aparecida Sebastião, Jefferson Elias-Oliveira, Vânia Brazão, José Clóvis do Prado Júnior, Daniela Carlos, Cristina Ribeiro de Barros C
    Microorganisms.2023; 11(2): 460.     CrossRef
  • The Effects of Stress and Diet on the “Brain–Gut” and “Gut–Brain” Pathways in Animal Models of Stress and Depression
    Mauritz F. Herselman, Sheree Bailey, Larisa Bobrovskaya
    International Journal of Molecular Sciences.2022; 23(4): 2013.     CrossRef
  • Intestinal microbiota and melatonin in the treatment of secondary injury and complications after spinal cord injury
    Yiwen Zhang, Rui Lang, Shunyu Guo, Xiaoqin Luo, Huiting Li, Cencen Liu, Wei Dong, Changshun Bao, Yang Yu
    Frontiers in Neuroscience.2022;[Epub]     CrossRef
  • Protective Effects and Mechanisms of Melatonin on Stress Myocardial Injury in Rats
    Jia-yao Chen, Ting Li, Jiao-ling Wang, Zhan-le Wang, Yun Zhang, Lin-quan Zang
    Journal of Cardiovascular Pharmacology.2022; 80(3): 417.     CrossRef
  • Rescue of social deficits by early-life melatonin supplementation through modulation of gut microbiota in a murine model of autism
    Xia Liu, Yi Cui, Yuhan Zhang, Guo Xiang, Meng Yu, Xianshu Wang, Bin Qiu, Xin-gang Li, Wei Liu, Di Zhang
    Biomedicine & Pharmacotherapy.2022; 156: 113949.     CrossRef
  • Roles of PRR-Mediated Signaling Pathways in the Regulation of Oxidative Stress and Inflammatory Diseases
    Pengwei Li, Mingxian Chang
    International Journal of Molecular Sciences.2021; 22(14): 7688.     CrossRef
Review
[MINIREVIEW]Regulation of gene expression by protein lysine acetylation in Salmonella
Hyojeong Koo , Shinae Park , Min-Kyu Kwak , Jung-Shin Lee
J. Microbiol. 2020;58(12):979-987.   Published online November 17, 2020
DOI: https://doi.org/10.1007/s12275-020-0483-8
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AbstractAbstract PDF
Protein lysine acetylation influences many physiological functions, such as gene regulation, metabolism, and disease in eukaryotes. Although little is known about the role of lysine acetylation in bacteria, several reports have proposed its importance in various cellular processes. Here, we discussed the function of the protein lysine acetylation and the post-translational modifications (PTMs) of histone-like proteins in bacteria focusing on Salmonella pathogenicity. The protein lysine residue in Salmonella is acetylated by the Pat-mediated enzymatic pathway or by the acetyl phosphate-mediated non-enzymatic pathway. In Salmonella, the acetylation of lysine 102 and lysine 201 on PhoP inhibits its protein activity and DNAbinding, respectively. Lysine acetylation of the transcriptional regulator, HilD, also inhibits pathogenic gene expression. Moreover, it has been reported that the protein acetylation patterns significantly differ in the drug-resistant and -sensitive Salmonella strains. In addition, nucleoid-associated proteins such as histone-like nucleoid structuring protein (H-NS) are critical for the gene silencing in bacteria, and PTMs in H-NS also affect the gene expression. In this review, we suggest that protein lysine acetylation and the post-translational modifications of H-NS are important factors in understanding the regulation of gene expression responsible for pathogenicity in Salmonella.

Citations

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  • Global Insights into the Lysine Acetylome Reveal the Role of Lysine Acetylation in the Adaptation of Bacillus altitudinis to Salt Stress
    Xujian Li, Shanshan Dai, Shanshan Sun, Dongying Zhao, Hui Li, Junyi Zhang, Jie Ma, Binghai Du, Yanqin Ding
    Journal of Proteome Research.2025; 24(1): 210.     CrossRef
  • The concentration of medium-chain fatty acids in breast milk is influenced by maternal diet and associated with gut microbiota in infants
    Menglu Xi, Ignatius Man-Yau Szeto, Sufang Duan, Ting Li, Yalu Yan, Xia Ma, Ting Sun, Weilian Hung, Celi Yang, Yonghua Zhang, Ai Zhao
    Journal of Functional Foods.2025; 128: 106782.     CrossRef
  • Reversible acetylation of ribosomal protein S1 serves as a smart switch for Salmonella to rapidly adapt to host stress
    Yi-Lin Shen, Tian-Xian Liu, Lei Xu, Bang-Ce Ye, Ying Zhou
    Nucleic Acids Research.2025;[Epub]     CrossRef
  • Bacterial protein acetylation: mechanisms, functions, and methods for study
    Jocelin Rizo, Sergio Encarnación-Guevara
    Frontiers in Cellular and Infection Microbiology.2024;[Epub]     CrossRef
  • Acetyl-proteome profiling revealed the role of lysine acetylation in erythromycin resistance of Staphylococcus aureus
    Miao Feng, Xiaoyu Yi, Yanling Feng, Feng He, Zonghui Xiao, Hailan Yao
    Heliyon.2024; 10(15): e35326.     CrossRef
  • Short-chain fatty acids in breast milk and their relationship with the infant gut microbiota
    Menglu Xi, Yalu Yan, Sufang Duan, Ting Li, Ignatius Man-Yau Szeto, Ai Zhao
    Frontiers in Microbiology.2024;[Epub]     CrossRef
  • Acetylomics reveals an extensive acetylation diversity within Pseudomonas aeruginosa
    Nand Broeckaert, Hannelore Longin, Hanne Hendrix, Jeroen De Smet, Mirita Franz-Wachtel, Boris Maček, Vera van Noort, Rob Lavigne
    microLife.2024;[Epub]     CrossRef
  • Lysine acetylation regulates the AT-rich DNA possession ability of H-NS
    Yabo Liu, Mengqing Zhou, Yifan Bu, Liang Qin, Yuanxing Zhang, Shuai Shao, Qiyao Wang
    Nucleic Acids Research.2024; 52(4): 1645.     CrossRef
  • Acetylation of K188 and K192 inhibits the DNA-binding ability of NarL to regulate Salmonella virulence
    Liu-Qing Zhang, Yi-Lin Shen, Bang-Ce Ye, Ying Zhou, Christopher A. Elkins
    Applied and Environmental Microbiology.2023;[Epub]     CrossRef
  • Acetylome and Succinylome Profiling of Edwardsiella tarda Reveals Key Roles of Both Lysine Acylations in Bacterial Antibiotic Resistance
    Yuying Fu, Lishan Zhang, Huanhuan Song, Junyan Liao, Li Lin, Wenjia Jiang, Xiaoyun Wu, Guibin Wang
    Antibiotics.2022; 11(7): 841.     CrossRef
  • Pat- and Pta-mediated protein acetylation is required for horizontally-acquired virulence gene expression in Salmonella Typhimurium
    Hyojeong Koo, Eunna Choi, Shinae Park, Eun-Jin Lee, Jung-Shin Lee
    Journal of Microbiology.2022; 60(8): 823.     CrossRef
  • Acetylation of CspC Controls the Las Quorum-Sensing System through Translational Regulation of rsaL in Pseudomonas aeruginosa
    Shouyi Li, Xuetao Gong, Liwen Yin, Xiaolei Pan, Yongxin Jin, Fang Bai, Zhihui Cheng, Un-Hwan Ha, Weihui Wu, Pierre Cornelis, Gerald B. Pier
    mBio.2022;[Epub]     CrossRef
  • Trans-acting regulators of ribonuclease activity
    Jaejin Lee, Minho Lee, Kangseok Lee
    Journal of Microbiology.2021; 59(4): 341.     CrossRef
  • Acetylation of the CspA family protein CspC controls the type III secretion system through translational regulation ofexsAinPseudomonas aeruginosa
    Shouyi Li, Yuding Weng, Xiaoxiao Li, Zhuo Yue, Zhouyi Chai, Xinxin Zhang, Xuetao Gong, Xiaolei Pan, Yongxin Jin, Fang Bai, Zhihui Cheng, Weihui Wu
    Nucleic Acids Research.2021; 49(12): 6756.     CrossRef
  • Transcriptional Regulation of the Multiple Resistance Mechanisms in Salmonella—A Review
    Michał Wójcicki, Olga Świder, Kamila J. Daniluk, Paulina Średnicka, Monika Akimowicz, Marek Ł. Roszko, Barbara Sokołowska, Edyta Juszczuk-Kubiak
    Pathogens.2021; 10(7): 801.     CrossRef
Journal Articles
Phosphorylation of tegument protein pp28 contributes to trafficking to the assembly compartment in human cytomegalovirus infection
Jun-Young Seo , Jin Ah Heo , William J. Britt
J. Microbiol. 2020;58(7):624-631.   Published online June 27, 2020
DOI: https://doi.org/10.1007/s12275-020-0263-5
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AbstractAbstract PDF
Human cytomegalovirus (HCMV) UL99 encodes a late tegument protein pp28 that is essential for envelopment and production of infectious virus. This protein is localized to the endoplasmic reticulum-Golgi intermediate compartment (ERGIC) in transfected cells but it localizes to the cytoplasmic assembly compartment (AC) in HCMV-infected cells. Trafficking of pp28 to the AC is required for the assembly of infectious virus. The N-terminal domain (aa 1-61) of pp28 is sufficient for trafficking and function of the wild type protein during viral infection. However, residues required for authentic pp28 trafficking with the exception of the acidic cluster in the N-terminal domain of pp28 remain undefined. Monitoring protein migration on SDS-PAGE, we found that pp28 is phosphorylated in the virus-infected cells and dephosphorylated in the viral particles. By generating substitution mutants of pp28, we showed that three serine residues (aa 41–43) and a tyrosine residue (aa 34) account for its phosphorylation. The mutant forms of pp28 were localized to the plasma membrane as well as the ERGIC in transfected cells. Likewise, these mutant proteins were localized to the plasma membrane as well as the AC in virus-infected cells. These results suggested that phosphorylation of pp28 contributes to its intracellular trafficking and efficient viral assembly and incorporation.

Citations

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  • Exploring the genetic associations and causal relationships between antibody responses, immune cells, and various types of breast cancer
    Yang Yang, Jiayi Chen, Fuhong Gong, Jingge Miao, Mengping Lin, Ruimin Liu, Chenxi Wang, Fei Ge, Wenlin Chen
    Scientific Reports.2024;[Epub]     CrossRef
  • Human cytomegalovirus induces significant structural and functional changes in terminally differentiated human cortical neurons
    Jacob W. Adelman, Suzette Rosas-Rogers, Megan L. Schumacher, Rebekah L. Mokry, Scott S. Terhune, Allison D. Ebert, Thomas Shenk
    mBio.2023;[Epub]     CrossRef
  • Insights into the Transcriptome of Human Cytomegalovirus: A Comprehensive Review
    Janine Zeng, Di Cao, Shaomin Yang, Dabbu Kumar Jaijyan, Xiaolian Liu, Songbin Wu, Ruth Cruz-Cosme, Qiyi Tang, Hua Zhu
    Viruses.2023; 15(8): 1703.     CrossRef
  • Features and Functions of the Conserved Herpesvirus Tegument Protein UL11 and Its Binding Partners
    Linjiang Yang, Mingshu Wang, Anchun Cheng, Qiao Yang, Ying Wu, Juan Huang, Bin Tian, Renyong Jia, Mafeng Liu, Dekang Zhu, Shun Chen, Xinxin Zhao, Shaqiu Zhang, Xumin Ou, Sai Mao, Qun Gao, Di Sun
    Frontiers in Microbiology.2022;[Epub]     CrossRef
  • The human cytomegalovirus decathlon: Ten critical replication events provide opportunities for restriction
    Declan L. Turner, Rommel A. Mathias
    Frontiers in Cell and Developmental Biology.2022;[Epub]     CrossRef
Light affects picocyanobacterial grazing and growth response of the mixotrophic flagellate Poterioochromonas malhamensis
Thomas Weisse , Michael Moser
J. Microbiol. 2020;58(4):268-278.   Published online January 28, 2020
DOI: https://doi.org/10.1007/s12275-020-9567-8
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AbstractAbstract PDF
We measured the grazing and growth response of the mixotrophic chrysomonad flagellate Poterioochromonas malhamensis on four closely related picocyanobacterial strains isolated from subalpine lakes in central Europe. The picocyanobacteria represented different pigment types (phycoerythrin- rich, PE, and phycocyanin-rich, PC) and phylogenetic clusters. The grazing experiments were conducted with laboratory cultures acclimated to 10 μmol photon/m2/sec (low light, LL) and 100 μmol photon/m2/sec (moderate light, ML), either in the dark or at four different irradiances ranging from low (6 μmol photon/m2/sec) to high (1,500 μmol photon/m2/ sec) light intensity. Poterioochromonas malhamensis preferred the larger, green PC-rich picocyanobacteria to the smaller, red PE-rich picocyanobacterial, and heterotrophic bacteria. The feeding and growth rates of P. malhamensis were sensitive to the actual light conditions during the experiments; the flagellate performed relatively better in the dark and at LL conditions than at high light intensity. In summary, our
results
found strain-specific ingestion and growth rates of the flagellate; an effect of the preculturing conditions, and, unexpectedly, a direct adverse effect of high light levels. We conclude that this flagellate may avoid exposure to high surface light intensities commonly encountered in temperate lakes during the summer.

Citations

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  • A systematic review of the predatory contaminant Poterioochromonas in microalgal culture
    Mingyang Ma, Chaojun Wei, Wenjie Huang, Yue He, Yingchun Gong, Qiang Hu
    Journal of Applied Phycology.2023; 35(3): 1103.     CrossRef
  • Transcriptional profile reveals the physiological responses to prey availability in the mixotrophic chrysophyte Poterioochromonas malhamensis
    Mingyang Ma, Wentao Yang, Hong Chen, Wanwan Ke, Yingchun Gong, Qiang Hu
    Frontiers in Microbiology.2023;[Epub]     CrossRef
  • Microbial consortia in an ice‐covered high‐altitude lake impacted by additions of dissolved organic carbon and nutrients
    Flavia Dory, Laurent Cavalli, Evelyne Franquet, Magalie Claeys‐Bruno, Benjamin Misson, Thierry Tatoni, Céline Bertrand
    Freshwater Biology.2021; 66(8): 1648.     CrossRef
  • Picoplankton feeding by the ciliate Vorticella similis in comparison to other peritrichs emphasizes their significance in the water purification process
    Thomas Weisse, Jitka Jezberova, Michael Moser
    Ecological Indicators.2021; 121: 106992.     CrossRef
Overexpression and characterization of a novel cold-adapted and salt-tolerant GH1 β-glucosidase from the marine bacterium Alteromonas sp. L82
Jingjing Sun , Wei Wang , Congyu Yao , Fangqun Dai , Xiangjie Zhu , Junzhong Liu , Jianhua Hao
J. Microbiol. 2018;56(9):656-664.   Published online August 23, 2018
DOI: https://doi.org/10.1007/s12275-018-8018-2
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AbstractAbstract PDF
A novel gene (bgl) encoding a cold-adapted β-glucosidase was cloned from the marine bacterium Alteromonas sp. L82. Based on sequence analysis and its putative catalytic conserved region, Bgl belonged to the glycoside hydrolase family 1. Bgl was overexpressed in E. coli and purified by Ni2+ affinity chromatography. The purified recombinant β- glucosidase showed maximum activity at temperatures between 25°C to 45°C and over the pH range 6 to 8. The enzyme lost activity quickly after incubation at 40°C. Therefore, recombinant β-glucosidase appears to be a cold-adapted enzyme. The addition of reducing agent doubled its activity and 2 M NaCl did not influence its activity. Recombinant β-glucosidase was also tolerant of 700 mM glucose and some organic solvents. Bgl had a Km of 0.55 mM, a Vmax of 83.6 U/mg, a kcat of 74.3 s-1 and kcat/Km of 135.1 at 40°C, pH 7 with 4-nitrophenyl-β-D-glucopyranoside as a substrate. These properties indicate Bgl may be an interesting candidate for biotechnological and industrial applications.

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  • A novel cold-active GH1 β-galactosidase from psychrotolerant Microbacterium phyllosphaerae LW106 suitable for lactose hydrolysis and galactooligosaccharides synthesis in milk at low temperature
    Aiguo Li, Wenlu Liu, Xuehua Yu, Rui Han, Xinyu Xiong, Bo Guan, Youzhen Hu, Yongqin Ni, Jun Zeng
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    Bo Liu, Haoyue Gu, Rui Shi, Xiahong He, Zhanbin Sun, Qing Ren, Hanxu Pan
    International Journal of Systematic and Evolutionary Microbiology .2024;[Epub]     CrossRef
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    Jingjing Sun, Wei Wang, Jianhua Hao
    Process Biochemistry.2024; 140: 108.     CrossRef
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    Qian Yao, Jin Xu, Nan Tang, Weiji Chen, Quliang Gu, He Li
    Environmental Research.2024; 244: 117676.     CrossRef
  • Characterization of a novel cold-adapted GH1 β-glucosidase from Psychrobacillus glaciei and its application in the hydrolysis of soybean isoflavone glycosides
    Jinjian He, Jiajing Duan, Pinglian Yu, Yuying Li, Mansheng Wang, Xiu Zhang, Zishu Chen, Pengjun Shi
    Current Research in Food Science.2024; 8: 100777.     CrossRef
  • Biochemical and in silico structural properties of a thermo-acid stable β-glucosidase from Beauveria bassiana
    Buka Magwaza, Ayodeji Amobonye, Prashant Bhagwat, Santhosh Pillai
    Heliyon.2024; 10(7): e28667.     CrossRef
  • Moderately thermostable GH1 β-glucosidases from hyperacidophilic archaeon Cuniculiplasma divulgatum S5
    Anna N Khusnutdinova, Hai Tran, Saloni Devlekar, Marco A Distaso, Ilya V Kublanov, Tatiana Skarina, Peter Stogios, Alexei Savchenko, Manuel Ferrer, Olga V Golyshina, Alexander F Yakunin, Peter N Golyshin
    FEMS Microbiology Ecology.2024;[Epub]     CrossRef
  • Structural determinants of cold activity and glucose tolerance of a family 1 glycoside hydrolase (GH1) from Antarctic Marinomonas sp. ef1
    Louise Jane Gourlay, Marco Mangiagalli, Elisabetta Moroni, Marina Lotti, Marco Nardini
    The FEBS Journal.2024; 291(13): 2897.     CrossRef
  • Partial characterization of β-glucosidase, β-xylosidase, and α-l-arabinofuranosidase from Jiangella alba DSM 45237 and their potential in lignocellulose-based biorefining
    Zeynep Gül Aytaş, Münir Tunçer, Çağrı Seda Kul, Sümeyye Cilmeli, Nurayan Aydın, Tuğrul Doruk, Ali Osman Adıgüzel
    Sustainable Chemistry and Pharmacy.2023; 31: 100900.     CrossRef
  • Heterologous expression and characterization of salt-tolerant β-glucosidase from xerophilic Aspergillus chevalieri for hydrolysis of marine biomass
    Hironori Senba, Daisuke Saito, Yukihiro Kimura, Shinichi Tanaka, Mikiharu Doi, Shinji Takenaka
    Archives of Microbiology.2023;[Epub]     CrossRef
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Research Support, Non-U.S. Gov'ts
Molecular characterization of mammalian-adapted Korean-type avian H9N2 virus and evaluation of its virulence in mice
Kuk Jin Park , Min-Suk Song , Eun-Ha Kim , Hyeok-il Kwon , Yun Hee Baek , Eun-hye Choi , Su-Jin Park , Se Mi Kim , Young-il Kim , Won-Suk Choi , Dae-Won Yoo , Chul-Joong Kim , Young Ki Choi
J. Microbiol. 2015;53(8):570-577.   Published online July 31, 2015
DOI: https://doi.org/10.1007/s12275-015-5329-4
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AbstractAbstract
Avian influenza A virus (AIV) is commonly isolated from domestic poultry and wild migratory birds, and the H9N2 subtype is the most prevalent and the major cause of severe disease in poultry in Korea. In addition to the veterinary concerns regarding the H9N2 subtype, it is also considered to be the next potential human pandemic strain due to its rapid evolution and interspecies transmission. In this study, we utilize serial lung-to-lung passage of a low pathogenic avian influenza virus (LPAI) H9N2 (A/Ck/Korea/163/04, WT163) (Y439-lineage) in mice to increase pathogenicity and investigate the potential virulence marker. Mouse-adapted H9N2 virus obtained high virulence (100% mortality) in mice after 98 serial passages. Sequence results show that the mouse adaptation (ma163) possesses several mutations within seven gene segments (PB2, PA, HA, NP, NA, M, and NS) relative to the wild-type strain. The HA gene showed the most mutations (at least 11) with one resulting in the loss of an N-glycosylation site (at amino acid 166). Moreover, reverse genetic studies established that an E627K substitution in PB2 and the loss of the N-glycosylation site in the HA protein (aa166) are critical virulence markers in the mouse-adapted H9N2 virus. Thus, these results add to the increasing body of mutational analysis data defining the function of the viral polymerase and HA genes and their roles in mammalian host adaptation. To our knowledge, this is first report of the generation of a mammalian-adapted Korea H9N2 virus (Y493-lineages). Therefore, this study offers valuable insights into the molecular evolution of the LPAI Korean H9N2 in a new host and adds to the current knowledge of the molecular markers associated with increased virulence.

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DBA/2 Mouse as an Animal Model for Anti-influenza Drug Efficacy Evaluation
Jin Il Kim , Sehee Park , Sangmoo Lee , Ilseob Lee , Jun Heo , Min-Woong Hwang , Joon-Yong Bae , Donghwan Kim , Seok-Il Jang , Mee Sook Park , Man-Seong Park
J. Microbiol. 2013;51(6):866-871.   Published online December 19, 2013
DOI: https://doi.org/10.1007/s12275-013-3428-7
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AbstractAbstract PDF
Influenza viruses are seasonally recurring human pathogens. Vaccines and antiviral drugs are available for influenza. However, the viruses, which often change themselves via antigenic drift and shift, demand constant efforts to update vaccine antigens every year and develop new agents with broad-spectrum antiviral efficacy. An animal model is critical for such efforts. While most human influenza viruses are unable to kill BALB/c mice, some strains have been shown to kill DBA/2 mice without prior adaptation. Therefore, in this study, we explored the feasibility of employing DBA/2 mice as a model in the development of anti-influenza drugs. Unlike the BALB/c strain, DBA/2 mice were highly susceptible and could be killed with a relatively low titer (50% DBA/2 lethal dose = 102.83 plaque-forming units) of the A/ Korea/01/2009 virus (2009 pandemic H1N1 virus). When treated with a neuraminidase inhibitor, oseltamivir phosphate, infected DBA/2 mice survived until 14 days postinfection. The reduced morbidity of the infected DBA/2 mice was also consistent with the oseltamivir treatment. Taking these data into consideration, we propose that the DBA/2 mouse is an excellent animal model to evaluate antiviral efficacy against influenza infection and can be further utilized for combination therapies or bioactivity models of existing and newly developed anti-influenza drugs.

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Complete Genome of Leptospirillum ferriphilum ML-04 Provides Insight into Its Physiology and Environmental Adaptation
Shuang Mi , Jian Song , Jianqun Lin , Yuanyuan Che , Huajun Zheng , Jianqiang Lin
J. Microbiol. 2011;49(6):890-901.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1099-9
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AbstractAbstract PDF
Leptospirillum ferriphilum has been identified as the dominant, moderately thermophilic, bioleaching microorganism in bioleaching processes. It is an acidic and chemolithoautrophic bacterium that gains electrons from ferrous iron oxidation for energy production and cell growth. Genetic information about this microorganism has been limited until now, which has hindered its further exploration. In this study, the complete genome of L. ferripilum ML-04 is sequenced and annotated. The bacterium has a single circular chromosome of 2,406,157 bp containing 2,471 coding sequences (CDS), 2 rRNA operons, 48 tRNA genes, a large number of mobile genetic elements and 2 genomic islands. In silico analysis shows L. ferriphilum ML-04 fixes carbon through a reductive citric acid (rTCA) cycle, and obtains nitrogen through ammonium assimilation. The genes related to “cell envelope biogenesis, outer membrane” (6.9%) and “DNA replication, recombination and repair” (5.6%) are abundant, and a large number of genes related to heavy metal detoxification, oxidative and acidic stress defense, and signal transduction pathways were detected. The genomic plasticity, plentiful cell envelope components, inorganic element metabolic abilities and stress response mechanisms found the base for this organism’s survival in the bioleaching niche.

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Adaptation and Cross-Adaptation of Listeria monocytogenes and Salmonella enterica to Poultry Decontaminants
Alicia Alonso-Hernando , Rosa Capita , Miguel Prieto , Carlos Alonso-Calleja
J. Microbiol. 2009;47(2):142-146.   Published online May 2, 2009
DOI: https://doi.org/10.1007/s12275-008-0237-5
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AbstractAbstract PDF
Information on the potential for acquired reduced susceptibility of bacteria to poultry decontaminants occurring is lacking. Minimal Inhibitory Concentrations (MICs) were established for assessing the initial susceptibility and the adaptative and cross-adaptative responses of four bacterial strains (Listeria monocytogenes serovar 1/2a, L. monocytogenes serovar 4b, Salmonella enterica serotype Typhimurium, and S. enterica serotype Enteritidis) to four poultry decontaminants (trisodium phosphate, acidified sodium chlorite -ASC-, citric acid, and peroxyacetic acid). The initial susceptibility was observed to differ among species (all decontaminants) and between Salmonella strains (ASC). These inter- and intra-specific variations highlight (1) the need for strict monitoring of decontaminant concentrations to inactivate all target pathogens of concern, and (2) the importance of selecting adequate test strains in decontamination studies. MICs of ASC (0.17±0.02 to 0.21±0.02 mg/ml) were higher than the U.S. authorized concentration when applied as a pre-chiller or chiller solution (0.05 to 0.15 mg/ml). Progressively increasing decontaminant concentrations resulted in reduced susceptibility of strains. The highest increase in MIC was 1.88 to 2.71-fold (ASC). All decontaminants were shown to cause cross-adaptation of strains between both related and unrelated compounds, the highest increase in MIC being 1.82-fold (ASC). Our results suggest that the in-use concentrations of ASC could, in certain conditions, be ineffective against Listeria and Salmonella strains. The adaptative and cross-adaptative responses of strains tested to poultry decontaminants are of minor concern. However, the observations being presented here are based on in vitro studies, and further research into practical applications are needed in order to confirm these findings.

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  • Exposure to Low Doses of Biocides Increases Resistance to Other Biocides and to Antibiotics in Strains of Listeria monocytogenes
    Cristina Rodríguez-Melcón, Rosa Capita, Carlos Alonso-Calleja
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Identification and Expression of the cym, cmt, and tod Catabolic Genes from Pseudomonas putida KL47: Expression of the Regulatory todST Genes as a Factor for Catabolic Adaptation
Kyoung Lee , Eun Kyeong Ryu , Kyung Soon Choi , Min Chul Cho , Jae Jun Jeong , Eun Na Choi , Soo O Lee , Do-Young Yoon , Ingyu Hwang , Chi-Kyung Kim
J. Microbiol. 2006;44(2):192-199.
DOI: https://doi.org/2365 [pii]
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AbstractAbstract PDF
Pseudomonas putida KL47 is a natural isolate that assimilates benzene, 1-alkylbenzene (C1-C4), biphenyl, p-cumate, and p-cymene. The genetic background of strain KL47 underlying the broad range of growth substrates was examined. It was found that the cym and cmt operons are constitutively expressed due to a lack of the cymR gene, and the tod operon is still inducible by toluene and biphenyl. The entire array of gene clusters responsible for the catabolism of toluene and p-cymene/p-cumate has been cloned in a cosmid vector, pLAFR3, and were named pEK6 and pEK27, respectively. The two inserts overlap one another and the nucleotide sequence (42,505 bp) comprising the cym, cmt, and tod operons and its flanking genes in KL47 are almost identical (>99%) to those of P. putida F1. In the cloned DNA fragment, two genes with unknown functions, labeled cymZ and cmtR, were newly identified and show high sequence homology to dienelactone hydrolase and CymR proteins, respectively. The cmtR gene was identified in the place of the cmtI gene of previous annotation. Western blot analysis showed that, in strains F1 and KL47, the todT gene is not expressed during growth on Luria Bertani medium. In minimal basal salt medium, expression of the todT gene is inducible by toluene, but not by biphenyl in strain F1; however, it is constantly expressed in strain KL47, indicating that high levels of expression of the todST genes with one amino acid substitution in TodS might provide strain KL47 with a means of adaptation of the tod catabolic operon to various aromatic hydrocarbons.
Review
The Use of the Rare UUA Codon to Define "Expression Space" for Genes Involved in Secondary Metabolism, Development and Environmental Adaptation in Streptomyces
Keith F. Chater , Govind Chandra
J. Microbiol. 2008;46(1):1-11.
DOI: https://doi.org/10.1007/s12275-007-0233-1
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AbstractAbstract PDF
In Streptomyces coelicolor, bldA encodes the only tRNA for a rare leucine codon, UUA. This tRNA is unnecessary for growth, but is required for some aspects of secondary metabolism and morphological development, as revealed by the phenotypes of bldA mutants in diverse streptomycetes. This article is a comprehensive review of out understanding of this unusual situation. Based on information from four sequenced genomes it now appears that, typically, about 2~3% of genes in any one streptomycete contain a TTA codon, most having been acquired through species-specific horizontal gene transfer. Among the few widely conserved TTA-containing genes, mutations in just one, the pleiotropic regulatory gene adpA, give an obvious phenotype: such mutants are defective in aerial growth and sporulation, but vary in the extent of their impairment in secondary metabolism in different streptomycetes. The TTA codon in adpA is largely responsible for the morphological phenotype of a bldA mutant of S. coelicolor. AdpA-dependent targets include several genes involved in the integrated action of extracellular proteases that, at least in some species, are involved in the conversion of primary biomass into spores. The effects of bldA mutations on secondary metabolism are mostly attributable to the presence of TTA codons in pathway-specific genes, particularly in transcriptional activator genes. This is not confined to S. coelicolor-it is true for about half of all known antibiotic biosynthetic gene sets from streptomycetes. Combined microarray and proteomic analysis of liquid (and therefore non-sporulating) S. coelicolor bldA mutant cultures revealed effects of the mutation during rapid growth, during transition phase, and in stationary phase. Some of these effects may be secondary consequences of changes in the pattern of ppGpp accumulation. It is argued that the preferential accumulation of the bldA tRNA under conditions in which growth is significantly constrained has evolved to favour the expression of genes that confer adaptive benefits in intermittently encountered sub-optimal environments. The evolution of this system may have been a secondary consequence of the selective pressure exerted by bacteriophage attack. Some biotechnological implications of bldA phenomenology are considered.

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  • Interplay between Non-Coding RNA Transcription, Stringent/Relaxed Phenotype and Antibiotic Production in Streptomyces ambofaciens
    Eva Pinatel, Matteo Calcagnile, Adelfia Talà, Fabrizio Damiano, Luisa Siculella, Clelia Peano, Giuseppe Egidio De Benedetto, Antonio Pennetta, Gianluca De Bellis, Pietro Alifano
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  • Transcriptional Regulation of Congocidine (Netropsin) Biosynthesis and Resistance
    Audrey Vingadassalon, Florence Lorieux, Maud Juguet, Alba Noël, Luisa D. F. Santos, Laura Marin Fernandez, Jean-Luc Pernodet, Stéphanie Bury-Moné, Sylvie Lautru, Maia Kivisaar
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  • AdpA Positively Regulates Morphological Differentiation and Chloramphenicol Biosynthesis in Streptomyces venezuelae
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  • The Use of the Rare TTA Codon in Streptomyces Genes: Significance of the Codon Context?
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    Indian Journal of Microbiology.2021; 61(1): 24.     CrossRef
  • Activation of cryptic milbemycin A4 production in Streptomyces sp. BB47 by the introduction of a functional bldA gene
    Nana Matsui, Shizuka Kawakami, Dai Hamamoto, Sayuri Nohara, Reina Sunada, Watanalai Panbangred, Yasuhiro Igarashi, Takuya Nihira, Shigeru Kitani
    The Journal of General and Applied Microbiology.2021; 67(6): 240.     CrossRef
  • The Phosin PptA Plays a Negative Role in the Regulation of Antibiotic Production in Streptomyces lividans
    Noriyasu Shikura, Emmanuelle Darbon, Catherine Esnault, Ariane Deniset-Besseau, Delin Xu, Clara Lejeune, Eric Jacquet, Naima Nhiri, Laila Sago, David Cornu, Sebastiaan Werten, Cécile Martel, Marie-Joelle Virolle
    Antibiotics.2021; 10(3): 325.     CrossRef
  • The Streptomyces filipinensis Gamma-Butyrolactone System Reveals Novel Clues for Understanding the Control of Secondary Metabolism
    Eva G. Barreales, Tamara D. Payero, Ester Jambrina, Jesús F. Aparicio, Rebecca E. Parales
    Applied and Environmental Microbiology.2020;[Epub]     CrossRef
  • Phenazine-1-carboxylic acid-producing Pseudomonas synxantha LBUM223 alters the transcriptome of Streptomyces scabies, the causal agent of potato common scab
    Tanya Arseneault, Roxane Roquigny, Amy Novinscak, Claudia Goyer, Martin Filion
    Physiological and Molecular Plant Pathology.2020; 110: 101480.     CrossRef
  • The Identification and Conservation of Tunicaminyluracil-Related Biosynthetic Gene Clusters in Several Rathayibacter Species Collected From Australia, Africa, Eurasia, and North America
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    Frontiers in Microbiology.2020;[Epub]     CrossRef
  • Gene miaA for post‐transcriptional modification of tRNAXXA is important for morphological and metabolic differentiation in Streptomyces
    Oksana Koshla, Oleksandr Yushchuk, Iryna Ostash, Yuriy Dacyuk, Maksym Myronovskyi, Gunilla Jäger, Roderich D. Süssmuth, Andriy Luzhetskyy, Anders Byström, Leif A. Kirsebom, Bohdan Ostash
    Molecular Microbiology.2019; 112(1): 249.     CrossRef
  • Gene ssfg_01967 (miaB) for tRNA modification influences morphogenesis and moenomycin biosynthesis in Streptomyces ghanaensis ATCC14672
    Yuliia Sehin, Oksana Koshla, Yuriy Dacyuk, Ruoxia Zhao, Robert Ross, Maksym Myronovskyi, Patrick A. Limbach, Andriy Luzhetskyy, Suzanne Walker, Victor Fedorenko, Bohdan Ostash
    Microbiology.2019; 165(2): 233.     CrossRef
  • LeuRS can leucylate type I and type II tRNALeus in Streptomyces coelicolor
    Jia-Yi Fan, Qian Huang, Quan-Quan Ji, En-Duo Wang
    Nucleic Acids Research.2019; 47(12): 6369.     CrossRef
  • Genome mining reveals the origin of a bald phenotype and a cryptic nucleocidin gene cluster in Streptomyces asterosporus DSM 41452
    Songya Zhang, Dennis Klementz, Jing Zhu, Roman Makitrynskyy, A.R. Ola Pasternak, Stefan Günther, David L. Zechel, Andreas Bechthold
    Journal of Biotechnology.2019; 292: 23.     CrossRef
  • Genomic Insights into Evolution of AdpA Family Master Regulators of Morphological Differentiation and Secondary Metabolism in Streptomyces
    Mariia Rabyk, Oleksandr Yushchuk, Ihor Rokytskyy, Maria Anisimova, Bohdan Ostash
    Journal of Molecular Evolution.2018; 86(3-4): 204.     CrossRef
  • Global regulator BldA regulates morphological differentiation and lincomycin production in Streptomyces lincolnensis
    Bingbing Hou, Liyuan Tao, Xiaoyu Zhu, Wei Wu, Meijin Guo, Jiang Ye, Haizhen Wu, Huizhan Zhang
    Applied Microbiology and Biotechnology.2018; 102(9): 4101.     CrossRef
  • Genome-guided exploration of metabolic features of Streptomyces peucetius ATCC 27952: past, current, and prospect
    Nguyen Huy Thuan, Dipesh Dhakal, Anaya Raj Pokhrel, Luan Luong Chu, Thi Thuy Van Pham, Anil Shrestha, Jae Kyung Sohng
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  • Rational engineering of Streptomyces albus J1074 for the overexpression of secondary metabolite gene clusters
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    Microbial Cell Factories.2018;[Epub]     CrossRef
  • In conditions of over-expression, WblI, a WhiB-like transcriptional regulator, has a positive impact on the weak antibiotic production of Streptomyces lividans TK24
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  • Tracking the Subtle Mutations Driving Host Sensing by the Plant Pathogen Streptomyces scabies
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    mSphere.2017;[Epub]     CrossRef
  • Properties of Streptomyces albus J1074 mutant deficient in tRNALeu UAA gene bldA
    Oksana Koshla, Maria Lopatniuk, Ihor Rokytskyy, Oleksandr Yushchuk, Yuriy Dacyuk, Victor Fedorenko, Andriy Luzhetskyy, Bohdan Ostash
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  • Genome Analysis of the Fruiting Body-Forming Myxobacterium Chondromyces crocatus Reveals High Potential for Natural Product Biosynthesis
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    Applied and Environmental Microbiology.2016; 82(6): 1945.     CrossRef
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  • Overexpression of a pathway specific negative regulator enhances production of daunorubicin in bldA deficient Streptomyces peucetius ATCC 27952
    Anaya Raj Pokhrel, Amit Kumar Chaudhary, Hue Thi Nguyen, Dipesh Dhakal, Tuoi Thi Le, Anil Shrestha, Kwangkyoung Liou, Jae Kyung Sohng
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  • Identification and engineering of regulation-related genes toward improved kasugamycin production
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    Applied Microbiology and Biotechnology.2016; 100(4): 1811.     CrossRef
  • Ribosomal frameshifting and transcriptional slippage: From genetic steganography and cryptography to adventitious use
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  • Development of an Unnatural Amino Acid Incorporation System in the Actinobacterial Natural Product Producer Streptomyces venezuelae ATCC 15439
    Jingxuan He, Briana Van Treeck, Han B. Nguyen, Charles E. Melançon
    ACS Synthetic Biology.2016; 5(2): 125.     CrossRef
  • The Rare Codon AGA Is Involved in Regulation of Pyoluteorin Biosynthesis in Pseudomonas protegens Pf-5
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  • Recent advances in understanding Streptomyces
    Keith F. Chater
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  • Changing Biosynthetic Profiles by Expressing bldA in Streptomyces Strains
    Arne Gessner, Tanja Heitzler, Songya Zhang, Christine Klaus, Renato Murillo, Hanna Zhao, Stephanie Vanner, David L. Zechel, Andreas Bechthold
    ChemBioChem.2015; 16(15): 2244.     CrossRef
  • Genome Mining of Streptomyces sp. Tü 6176: Characterization of the Nataxazole Biosynthesis Pathway
    Carolina Cano‐Prieto, Raúl García‐Salcedo, Marina Sánchez‐Hidalgo, Alfredo F. Braña, Hans‐Peter Fiedler, Carmen Méndez, José A. Salas, Carlos Olano
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  • Identification of BagI as a positive transcriptional regulator of bagremycin biosynthesis in engineered Streptomyces sp. Tü 4128
    Feng Liu, Dakui Xu, Yuchen Zhang, Yunxia Zhu, Jiang Ye, Huizhan Zhang
    Microbiological Research.2015; 173: 18.     CrossRef
  • Rifampicin-resistance, rpoB polymorphism and RNA polymerase genetic engineering
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  • Augmented genetic decoding: global, local and temporal alterations of decoding processes and codon meaning
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    Nature Reviews Genetics.2015; 16(9): 517.     CrossRef
  • The Gene bldA, a Regulator of Morphological Differentiation and Antibiotic Production in Streptomyces
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  • Genetic and Proteomic Analyses of Pupylation in Streptomyces coelicolor
    Corey L. Compton, Michael S. Fernandopulle, Rohith T. Nagari, Jason K. Sello, W. W. Metcalf
    Journal of Bacteriology.2015; 197(17): 2747.     CrossRef
  • c-di-GMP signalling and the regulation of developmental transitions in streptomycetes
    Matthew J. Bush, Natalia Tschowri, Susan Schlimpert, Klas Flärdh, Mark J. Buttner
    Nature Reviews Microbiology.2015; 13(12): 749.     CrossRef
  • Construction and development of a novel expression system of Streptomyces
    Chengran Guan, Wenjing Cui, Xiaotian He, Xu Hu, Jun Xu, Guocheng Du, Jian Chen, Zhemin Zhou
    Protein Expression and Purification.2015; 113: 17.     CrossRef
  • Identified members of the Streptomyces lividans AdpA regulon involved in differentiation and secondary metabolism
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    BMC Microbiology.2014;[Epub]     CrossRef
  • Thaxtomin A Production and Virulence Are Controlled by Several bld Gene Global Regulators in Streptomyces scabies
    Dawn R. D. Bignell, Isolde M. Francis, Joanna K. Fyans, Rosemary Loria
    Molecular Plant-Microbe Interactions®.2014; 27(8): 875.     CrossRef
  • Developmental biology ofStreptomycesfrom the perspective of 100 actinobacterial genome sequences
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    FEMS Microbiology Reviews.2014; 38(3): 345.     CrossRef
  • The gamma-butyrolactone receptors BulR1 and BulR2 of Streptomyces tsukubaensis: tacrolimus (FK506) and butyrolactone synthetases production control
    Zahra Salehi-Najafabadi, Carlos Barreiro, Antonio Rodríguez-García, Anthony Cruz, Gustavo E. López, Juan F. Martín
    Applied Microbiology and Biotechnology.2014; 98(11): 4919.     CrossRef
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  • Specificity determinants for the two tRNA substrates of the cyclodipeptide synthase AlbC from Streptomyces noursei
    M. Moutiez, J. Seguin, M. Fonvielle, P. Belin, I. B. Jacques, E. Favry, M. Arthur, M. Gondry
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    Journal of Industrial Microbiology and Biotechnology.2014; 41(2): 387.     CrossRef
  • Controlling translation elongation efficiency: tRNA regulation of ribosome flux on the mRNA
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    Biochemical Society Transactions.2014; 42(1): 160.     CrossRef
  • Collismycin A biosynthesis in Streptomyces sp. CS40 is regulated by iron levels through two pathway-specific regulators
    Natalia M. Vior, Carlos Olano, Ignacio García, Carmen Méndez, José A. Salas
    Microbiology.2014; 160(3): 467.     CrossRef
  • Genes Required for Aerial Growth, Cell Division, and Chromosome Segregation Are Targets of WhiA before Sporulation in Streptomyces venezuelae
    Matthew J. Bush, Maureen J. Bibb, Govind Chandra, Kim C. Findlay, Mark J. Buttner, Yves V. Brun
    mBio.2013;[Epub]     CrossRef
  • Pleiotropic regulatory genes bldA , adpA and absB are implicated in production of phosphoglycolipid antibiotic moenomycin
    Roman Makitrynskyy, Bohdan Ostash, Olga Tsypik, Yuriy Rebets, Emma Doud, Timothy Meredith, Andriy Luzhetskyy, Andreas Bechthold, Suzanne Walker, Victor Fedorenko
    Open Biology.2013; 3(10): 130121.     CrossRef
  • A Microbial Metagenome (Leucobactersp.) inCaenorhabditisWhole Genome Sequences
    Riccardo Percudani
    Bioinformatics and Biology Insights.2013; 7: BBI.S11064.     CrossRef
  • Molecular Regulation of Antibiotic Biosynthesis in Streptomyces
    Gang Liu, Keith F. Chater, Govind Chandra, Guoqing Niu, Huarong Tan
    Microbiology and Molecular Biology Reviews.2013; 77(1): 112.     CrossRef
  • Towards a new science of secondary metabolism
    Arryn Craney, Salman Ahmed, Justin Nodwell
    The Journal of Antibiotics.2013; 66(7): 387.     CrossRef
  • Recent advances in the biosynthesis of penicillins, cephalosporins and clavams and its regulation
    Gulay Ozcengiz, Arnold L. Demain
    Biotechnology Advances.2013; 31(2): 287.     CrossRef
  • 5S Clavam Biosynthesis Is Controlled by an Atypical Two-Component Regulatory System in Streptomyces clavuligerus
    Thomas Kwong, Nathan J. Zelyas, Hui Cai, Kapil Tahlan, Annie Wong, Susan E. Jensen
    Antimicrobial Agents and Chemotherapy.2012; 56(9): 4845.     CrossRef
  • Interspecies modulation of bacterial development through iron competition and siderophore piracy
    Matthew F. Traxler, Mohammad R. Seyedsayamdost, Jon Clardy, Roberto Kolter
    Molecular Microbiology.2012; 86(3): 628.     CrossRef
  • FK506 biosynthesis is regulated by two positive regulatory elements in Streptomyces tsukubaensis
    Dušan Goranovič, Marko Blažič, Vasilka Magdevska, Jaka Horvat, Enej Kuščer, Tomaž Polak, Javier Santos-Aberturas, Miriam Martínez-Castro, Carlos Barreiro, Peter Mrak, Gregor Kopitar, Gregor Kosec, Štefan Fujs, Juan F Martín, Hrvoje Petković
    BMC Microbiology.2012;[Epub]     CrossRef
  • Evaluation of Streptomyces coelicolor A3(2) as a heterologous expression host for the cyanobacterial protein kinase C activator lyngbyatoxin A
    Adam C. Jones, Sabine Ottilie, Alessandra S. Eustáquio, Daniel J. Edwards, Lena Gerwick, Bradley S. Moore, William H. Gerwick
    The FEBS Journal.2012; 279(7): 1243.     CrossRef
  • Signals and regulators that governStreptomycesdevelopment
    Joseph R. McCormick, Klas Flärdh
    FEMS Microbiology Reviews.2012; 36(1): 206.     CrossRef
  • Three pathway-specific regulators control streptolydigin biosynthesis in Streptomyces lydicus
    Cristina Gómez, Carlos Olano, Carmen Méndez, José A. Salas
    Microbiology.2012; 158(10): 2504.     CrossRef
  • Roles of fkbN in Positive Regulation and tcs7 in Negative Regulation of FK506 Biosynthesis in Streptomyces sp. Strain KCTC 11604BP
    SangJoon Mo, Young Ji Yoo, Yeon Hee Ban, Sung-Kwon Lee, Eunji Kim, Joo-Won Suh, Yeo Joon Yoon
    Applied and Environmental Microbiology.2012; 78(7): 2249.     CrossRef
  • Expression of the chaplin and rodlin hydrophobic sheath proteins in Streptomyces venezuelae is controlled by σBldN and a cognate anti‐sigma factor, RsbN
    Maureen J. Bibb, Ágota Domonkos, Govind Chandra, Mark J. Buttner
    Molecular Microbiology.2012; 84(6): 1033.     CrossRef
  • tRNA accumulation and suppression of the bldA phenotype during development in Streptomyces coelicolor
    B. M. Fredrik Pettersson, Leif A. Kirsebom
    Molecular Microbiology.2011; 79(6): 1602.     CrossRef
  • Novel Two-Component Systems Implied in Antibiotic Production in Streptomyces coelicolor
    Ana Yepes, Sergio Rico, Antonio Rodríguez-García, Ramón I. Santamaría, Margarita Díaz, Ching-Hong Yang
    PLoS ONE.2011; 6(5): e19980.     CrossRef
  • The regulation of the secondary metabolism of Streptomyces: new links and experimental advances
    Gilles P. van Wezel, Kenneth J. McDowall
    Natural Product Reports.2011; 28(7): 1311.     CrossRef
  • Strict regulation of morphological differentiation and secondary metabolism by a positive feedback loop between two global regulators AdpA and BldA in Streptomyces griseus
    Akiyoshi Higo, Sueharu Horinouchi, Yasuo Ohnishi
    Molecular Microbiology.2011; 81(6): 1607.     CrossRef
  • The Level of AdpA Directly Affects Expression of Developmental Genes in Streptomyces coelicolor
    Marcin Wolański, Rafał Donczew, Agnieszka Kois-Ostrowska, Paweł Masiewicz, Dagmara Jakimowicz, Jolanta Zakrzewska-Czerwińska
    Journal of Bacteriology.2011; 193(22): 6358.     CrossRef
  • SanG, a transcriptional activator, controls nikkomycin biosynthesis through binding to the sanN–sanO intergenic region in Streptomyces ansochromogenes
    Xihong He, Rui Li, Yuanyuan Pan, Gang Liu, Huarong Tan
    Microbiology .2010; 156(3): 828.     CrossRef
  • Differential proteomic analysis reveals novel links between primary metabolism and antibiotic production in Amycolatopsis balhimycina
    Giuseppe Gallo, Giovanni Renzone, Rosa Alduina, Efthimia Stegmann, Tilmann Weber, Anna Eliasson Lantz, Jette Thykaer, Fabio Sangiorgi, Andrea Scaloni, Anna Maria Puglia
    PROTEOMICS.2010; 10(7): 1336.     CrossRef
  • Adaptation of the Highly Productive T7 Expression System to Streptomyces lividans
    François-Xavier Lussier, François Denis, François Shareck
    Applied and Environmental Microbiology.2010; 76(3): 967.     CrossRef
  • Autoregulation of hpdR and its effect on CDA biosynthesis in Streptomyces coelicolor
    Haihua Yang, Yang An, Linqi Wang, Shuli Zhang, Yue Zhang, Yuqing Tian, Gang Liu, Huarong Tan
    Microbiology .2010; 156(9): 2641.     CrossRef
  • Regulation of the Biosynthesis of the Macrolide Antibiotic Spiramycin in Streptomyces ambofaciens
    Fatma Karray, Emmanuelle Darbon, Hoang Chuong Nguyen, Josette Gagnat, Jean-Luc Pernodet
    Journal of Bacteriology.2010; 192(21): 5813.     CrossRef
  • Moenomycin family antibiotics: chemical synthesis, biosynthesis, and biological activity
    Bohdan Ostash, Suzanne Walker
    Natural Product Reports.2010; 27(11): 1594.     CrossRef
  • Morphological differentiation and clavulanic acid formation are affected in a Streptomyces clavuligerus adpA-deleted mutant
    M. T. Lopez-Garcia, I. Santamarta, P. Liras
    Microbiology.2010; 156(8): 2354.     CrossRef
  • Quantitative Proteome Analysis of Streptomyces coelicolor Nonsporulating Liquid Cultures Demonstrates a Complex Differentiation Process Comparable to That Occurring in Sporulating Solid Cultures
    Angel Manteca, Hye R. Jung, Veit Schwämmle, Ole N. Jensen, Jesus Sanchez
    Journal of Proteome Research.2010; 9(9): 4801.     CrossRef
  • Genetically Engineered Lipopeptide Antibiotics Related to A54145 and Daptomycin with Improved Properties
    Kien T. Nguyen, Xiaowei He, Dylan C. Alexander, Chen Li, Jian-Qiao Gu, Carmela Mascio, Andrew Van Praagh, Larry Mortin, Min Chu, Jared A. Silverman, Paul Brian, Richard H. Baltz
    Antimicrobial Agents and Chemotherapy.2010; 54(4): 1404.     CrossRef
  • Genes essential for morphological development and antibiotic production in Streptomyces coelicolor are targets of BldD during vegetative growth
    Chris D. Den Hengst, Ngat T. Tran, Maureen J. Bibb, Govind Chandra, Brenda K. Leskiw, Mark J. Buttner
    Molecular Microbiology.2010; 78(2): 361.     CrossRef
  • The complex extracellular biology ofStreptomyces
    Keith F. Chater, Sandor Biró, Kye Joon Lee, Tracy Palmer, Hildgund Schrempf
    FEMS Microbiology Reviews.2010; 34(2): 171.     CrossRef
  • Streptomyces scabies 87-22 Contains a Coronafacic Acid-Like Biosynthetic Cluster That Contributes to Plant–Microbe Interactions
    Dawn R. D. Bignell, Ryan F. Seipke, José C. Huguet-Tapia, Alan H. Chambers, Ronald J. Parry, Rosemary Loria
    Molecular Plant-Microbe Interactions®.2010; 23(2): 161.     CrossRef
  • Characterization of γ-Butyrolactone Autoregulatory Signaling Gene Homologs in the Angucyclinone Polyketide WS5995B ProducerStreptomyces acidiscabies
    Frank G. Healy, Kevin P. Eaton, Prajit Limsirichai, Joel F. Aldrich, Alaina K. Plowman, Russell R. King
    Journal of Bacteriology.2009; 191(15): 4786.     CrossRef
  • The pleiotropic regulator AdpA‐L directly controls the pathway‐specific activator of nikkomycin biosynthesis in Streptomyces ansochromogenes
    Yuanyuan Pan, Gang Liu, Haihua Yang, Yuqing Tian, Huarong Tan
    Molecular Microbiology.2009; 72(3): 710.     CrossRef
  • The SmpB-tmRNA Tagging System Plays Important Roles in Streptomyces coelicolor Growth and Development
    Chunzhong Yang, John R. Glover, Christophe Herman
    PLoS ONE.2009; 4(2): e4459.     CrossRef
  • Deciphering Biosynthesis of the RNA Polymerase Inhibitor Streptolydigin and Generation of Glycosylated Derivatives
    Carlos Olano, Cristina Gómez, María Pérez, Martina Palomino, Antonio Pineda-Lucena, Rodrigo J. Carbajo, Alfredo F. Braña, Carmen Méndez, José A. Salas
    Chemistry & Biology.2009; 16(10): 1031.     CrossRef
  • Extracellular signalling, translational control, two repressors and an activator all contribute to the regulation of methylenomycin production inStreptomyces coelicolor
    Sean O'Rourke, Andreas Wietzorrek, Kay Fowler, Christophe Corre, Greg L. Challis, Keith F. Chater
    Molecular Microbiology.2009; 71(3): 763.     CrossRef
  • Evolutionary flux of potentially bldA-dependent Streptomyces genes containing the rare leucine codon TTA
    Govind Chandra, Keith F. Chater
    Antonie van Leeuwenhoek.2008; 94(1): 111.     CrossRef
  • novE and novG act as positive regulators of novobiocin biosynthesis
    Volker Dangel, Alessandra S. Eustáquio, Bertolt Gust, Lutz Heide
    Archives of Microbiology.2008; 190(5): 509.     CrossRef
  • SarA influences the sporulation and secondary metabolism inStreptomyces coelicolorM145
    Xijun Ou, Bo Zhang, Lin Zhang, Kai Dong, Chun Liu, Guoping Zhao, Xiaoming Ding
    Acta Biochimica et Biophysica Sinica.2008; 40(10): 877.     CrossRef

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