Skip Navigation
Skip to contents

Journal of Microbiology : Journal of Microbiology

OPEN ACCESS
SEARCH
Search

Search

Page Path
HOME > Search
4 "osmotic stress"
Filter
Filter
Article category
Keywords
Publication year
Journal Article
iTRAQ-facilitated proteomic analysis of Bacillus cereus via degradation of malachite green
Bobo Wang , Jing Lu , Junfang Zheng , Zhisheng Yu
J. Microbiol. 2021;59(2):142-150.   Published online February 1, 2021
DOI: https://doi.org/10.1007/s12275-021-0441-0
  • 57 View
  • 0 Download
  • 1 Web of Science
  • 1 Crossref
AbstractAbstract
The wide use of malachite green (MG) as a dye has caused substantial concern owing to its toxicity. Bacillus cereus can against the toxic effect of MG and efficiently decolourise it. However, detailed information regarding its underlying adaptation and degradation mechanisms based on proteomic data is scarce. In this study, the isobaric tags for relative and absolute quantitation (iTRAQ)-facilitated quantitative method was applied to analyse the molecular mechanisms by which B. cereus degrades MG. Based on this analysis, 209 upregulated proteins and 198 downregulated proteins were identified with a false discovery rate of 1% or less during MG biodegradation. Gene ontology and KEGG analysis determined that the differentially expressed proteins were enriched in metabolic processes, catalytic activity, antioxidant activity, and responses to stimuli. Furthermore, real-time qPCR was utilised to further confirm the regulated proteins involved in benzoate degradation. The proteins BCE_4076 (Acetyl-CoA acetyltransferase), BCE_5143 (Acetyl-CoA acetyltransferase), BCE_5144 (3-hydroxyacyl-CoA dehydrogenase), BCE_4651 (Enoyl-CoA hydratase), and BCE_5474 (3-hydroxyacyl-CoA dehydrogenase) involved in the benzoate degradation pathway may play an important role in the biodegradation of MG by B. cereus. The results of this study not only provide a comprehensive view of proteomic changes in B. cereus upon MG loading but also shed light on the mechanism underlying MG biodegradation by B. cereus.

Citations

Citations to this article as recorded by  
  • Engineering globins for efficient biodegradation of malachite green: two case studies of myoglobin and neuroglobin
    Jiao Liu, Jia-Kun Xu, Hong Yuan, Xiao-Juan Wang, Shu-Qin Gao, Ge-Bo Wen, Xiang-Shi Tan, Ying-Wu Lin
    RSC Advances.2022; 12(29): 18654.     CrossRef
Reviews
REVIEW] The contribution of Aspergillus fumigatus stress responses to virulence and antifungal resistance
Neil A. Brown , Gustavo H. Goldman
J. Microbiol. 2016;54(3):243-253.   Published online February 27, 2016
DOI: https://doi.org/10.1007/s12275-016-5510-4
  • 52 View
  • 0 Download
  • 53 Crossref
AbstractAbstract
Invasive aspergillosis has emerged as one of the most common life-threatening fungal disease of humans. The emergence of antifungal resistant pathogens represents a current and increasing threat to society. In turn, new strategies to combat fungal infection are urgently required. Fungal adaptations to stresses experienced within the human host are a prerequisite for the survival and virulence strategies of the pathogen. Here, we review the latest information on the signalling pathways in Aspergillus fumigatus that contribute to stress adaptations and virulence, while highlighting their potential as targets for the development of novel combinational antifungal therapies.

Citations

Citations to this article as recorded by  
  • The Expanding Mycovirome of Aspergilli
    Josephine L. Battersby, David A. Stevens, Robert H. A. Coutts, Vladimír Havlíček, Joe L. Hsu, Gabriele Sass, Ioly Kotta-Loizou
    Journal of Fungi.2024; 10(8): 585.     CrossRef
  • Synergistic effects of putative Ca2+-binding sites of calmodulin in fungal development, temperature stress and virulence ofAspergillus fumigatus
    Xingyue Li, Ruoyun Feng, Pan Luo, Yuanwei Zhang, Ling Lu
    Virulence.2024;[Epub]     CrossRef
  • MicroRNA (miRNA) profiling of maize genotypes with differential response to Aspergillus flavus implies zma-miR156–squamosa promoter binding protein (SBP) and zma-miR398/zma-miR394–F -box combinations involved in resistance mechanisms
    Prasad Gandham, Kanniah Rajasekaran, Christine Sickler, Harikrishnan Mohan, Matthew Gilbert, Niranjan Baisakh
    Stress Biology.2024;[Epub]     CrossRef
  • Pleiotropic functions of SscA on the asexual spore of the human pathogenic fungus Aspergillus fumigatus
    Ye-Eun Son, Jiwoo Han, Kyung-Tae Lee, Hee-Soo Park
    Mycology.2024; 15(2): 238.     CrossRef
  • The Oxidative Stress Response Highly Depends on Glucose and Iron Availability in Aspergillus fumigatus
    Tamás Emri, Károly Antal, Kinga Varga, Barnabás Csaba Gila, István Pócsi
    Journal of Fungi.2024; 10(3): 221.     CrossRef
  • Response of Fusarium oxysporum soil isolate to amphotericin B and fluconazole at the proteomic level
    I. V. da S. Amatto, F. A. de O. Simões, N. G. da R. Garzon, C. L. Marciano, R. R. da Silva, H. Cabral
    Brazilian Journal of Microbiology.2024; 55(3): 2557.     CrossRef
  • tRNA hypomodification facilitates 5-fluorocytosine resistance via cross-pathway control system activation in Aspergillus fumigatus
    Alexander Bruch, Valentina Lazarova, Maximilian Berg, Thomas Krüger, Sascha Schäuble, Abdulrahman A Kelani, Birte Mertens, Pamela Lehenberger, Olaf Kniemeyer, Stefanie Kaiser, Gianni Panagiotou, Fabio Gsaller, Matthew G Blango
    Nucleic Acids Research.2024;[Epub]     CrossRef
  • A host defense peptide mimetic, brilacidin, potentiates caspofungin antifungal activity against human pathogenic fungi
    Thaila Fernanda dos Reis, Patrícia Alves de Castro, Rafael Wesley Bastos, Camila Figueiredo Pinzan, Pedro F. N. Souza, Suzanne Ackloo, Mohammad Anwar Hossain, David Harold Drewry, Sondus Alkhazraji, Ashraf S. Ibrahim, Hyunil Jo, Jorge D. Lightfoot, Emily
    Nature Communications.2023;[Epub]     CrossRef
  • Pathogenicity and virulence of Aspergillus fumigatus
    Kayleigh Earle, Clara Valero, Daniel P. Conn, George Vere, Peter C. Cook, Michael J. Bromley, Paul Bowyer, Sara Gago
    Virulence.2023;[Epub]     CrossRef
  • Putative Core Transcription Factors Affecting Virulence in Aspergillus flavus during Infection of Maize
    Matthew K. Gilbert, Brian M. Mack, Matthew D. Lebar, Perng-Kuang Chang, Stephanie R. Gross, Rebecca R. Sweany, Jeffrey W. Cary, Kanniah Rajasekaran
    Journal of Fungi.2023; 9(1): 118.     CrossRef
  • Fungi’s Swiss Army Knife: Pleiotropic Effect of Melanin in Fungal Pathogenesis during Cattle Mycosis
    Víctor Romero, Carolina Kalinhoff, Luis Rodrigo Saa, Aminael Sánchez
    Journal of Fungi.2023; 9(9): 929.     CrossRef
  • Afu-Emi1 Contributes to Stress Adaptation and Voriconazole Susceptibility in Aspergillus fumigatus
    Jufang Tan, Heng Zhang, Yi Sun, Lujuan Gao, Cezar M. Khursigara
    Microbiology Spectrum.2023;[Epub]     CrossRef
  • COVID-19-Associated Pulmonary Aspergillosis Isolates Are Genomically Diverse but Similar to Each Other in Their Responses to Infection-Relevant Stresses
    Matthew E. Mead, Patrícia Alves de Castro, Jacob L. Steenwyk, Jean-Pierre Gangneux, Martin Hoenigl, Juergen Prattes, Riina Rautemaa-Richardson, Hélène Guegan, Caroline B. Moore, Cornelia Lass-Flörl, Florian Reizine, Clara Valero, Norman Van Rhijn, Michael
    Microbiology Spectrum.2023;[Epub]     CrossRef
  • Host-derived reactive oxygen species trigger activation of the Candida albicans transcription regulator Rtg1/3
    Mazen Oneissi, Melissa R. Cruz, Bernardo Ramírez-Zavala, Elena Lindemann-Perez, Joachim Morschhäuser, Danielle A. Garsin, J. Christian Perez, Aaron P. Mitchell
    PLOS Pathogens.2023; 19(9): e1011692.     CrossRef
  • The high osmolarity glycerol (HOG) pathway in fungi†
    Hajar Yaakoub, Norma Silvia Sanchez, Laura Ongay-Larios, Vincent Courdavault, Alphonse Calenda, Jean-Philippe Bouchara, Roberto Coria, Nicolas Papon
    Critical Reviews in Microbiology.2022; 48(6): 657.     CrossRef
  • Stress Responses Elicited by Glucose Withdrawal in Aspergillus fumigatus
    Tamás Emri, Károly Antal, Barnabás Gila, Andrea P. Jónás, István Pócsi
    Journal of Fungi.2022; 8(11): 1226.     CrossRef
  • PHYTONICIDIC PROPERTIES OF PLANTS REGARDING FUNGI OF THE ASPERGILLUS GENUS
    A. Karasenko, S. Peredera
    Sučasne ptahìvnictvo.2022;[Epub]     CrossRef
  • Strategies Shaping the Transcription of Carbohydrate-Active Enzyme Genes in Aspergillus nidulans
    Barnabás Cs. Gila, Károly Antal, Zsuzsanna Birkó, Judit Sz. Keserű, István Pócsi, Tamás Emri
    Journal of Fungi.2022; 8(1): 79.     CrossRef
  • An evolutionary genomic approach reveals both conserved and species-specific genetic elements related to human disease in closely related Aspergillus fungi
    Matthew E Mead, Jacob L Steenwyk, Lilian P Silva, Patrícia A de Castro, Nauman Saeed, Falk Hillmann, Gustavo H Goldman, Antonis Rokas, A Mitchell
    Genetics.2021;[Epub]     CrossRef
  • Flavonoids Modulate the Accumulation of Toxins From Aspergillus flavus in Maize Kernels
    Lina Castano-Duque, Matthew K. Gilbert, Brian M. Mack, Matthew D. Lebar, Carol H. Carter-Wientjes, Christine M. Sickler, Jeffrey W. Cary, Kanniah Rajasekaran
    Frontiers in Plant Science.2021;[Epub]     CrossRef
  • Novel Biological Functions of the NsdC Transcription Factor in Aspergillus fumigatus
    Patrícia Alves de Castro, Clara Valero, Jéssica Chiaratto, Ana Cristina Colabardini, Lakhansing Pardeshi, Lilian Pereira Silva, Fausto Almeida, Marina Campos Rocha, Roberto Nascimento Silva, Iran Malavazi, Wenyue Du, Paul S. Dyer, Matthias Brock, Flávio V
    mBio.2021;[Epub]     CrossRef
  • Fungal G-Protein-Coupled Receptors: A Promising Mediator of the Impact of Extracellular Signals on Biosynthesis of Ochratoxin A
    Jing Gao, Xinge Xu, Kunlun Huang, Zhihong Liang
    Frontiers in Microbiology.2021;[Epub]     CrossRef
  • The Essential Thioredoxin Reductase of the Human Pathogenic Mold Aspergillus fumigatus Is a Promising Antifungal Target
    Jasmin Binder, Yana Shadkchan, Nir Osherov, Sven Krappmann
    Frontiers in Microbiology.2020;[Epub]     CrossRef
  • Putative Membrane Receptors Contribute to Activation and Efficient Signaling of Mitogen-Activated Protein Kinase Cascades during Adaptation of Aspergillus fumigatus to Different Stressors and Carbon Sources
    Lilian Pereira Silva, Dean Frawley, Leandro José de Assis, Ciara Tierney, Alastair B. Fleming, Ozgur Bayram, Gustavo Henrique Goldman, Aaron P. Mitchell
    mSphere.2020;[Epub]     CrossRef
  • Evolving moldy murderers: Aspergillus section Fumigati as a model for studying the repeated evolution of fungal pathogenicity
    Antonis Rokas, Matthew E. Mead, Jacob L. Steenwyk, Nicholas H. Oberlies, Gustavo H. Goldman, Donald C. Sheppard
    PLOS Pathogens.2020; 16(2): e1008315.     CrossRef
  • Aspergillus fumigatus G-Protein Coupled Receptors GprM and GprJ Are Important for the Regulation of the Cell Wall Integrity Pathway, Secondary Metabolite Production, and Virulence
    Aílton Pereira da Costa Filho, Guilherme Thomaz Pereira Brancini, Patrícia Alves de Castro, Clara Valero, Jaire Alves Ferreira Filho, Lilian Pereira Silva, Marina Campos Rocha, Iran Malavazi, João Guilherme de Moraes Pontes, Taícia Fill, Roberto Nasciment
    mBio.2020;[Epub]     CrossRef
  • Phenotypic plasticity and the evolution of azole resistance in Aspergillus fumigatus; an expression profile of clinical isolates upon exposure to itraconazole
    Margriet W. J. Hokken, Jan Zoll, Jordy P. M. Coolen, Bas J. Zwaan, Paul E. Verweij, Willem J. G. Melchers
    BMC Genomics.2019;[Epub]     CrossRef
  • Aspergillus fumigatus calcium-responsive transcription factors regulate cell wall architecture promoting stress tolerance, virulence and caspofungin resistance
    Patrícia Alves de Castro, Ana Cristina Colabardini, Adriana Oliveira Manfiolli, Jéssica Chiaratto, Lilian Pereira Silva, Eliciane Cevolani Mattos, Giuseppe Palmisano, Fausto Almeida, Gabriela Felix Persinoti, Laure Nicolas Annick Ries, Laura Mellado, Mari
    PLOS Genetics.2019; 15(12): e1008551.     CrossRef
  • How Environmental Fungi Cause a Range of Clinical Outcomes in Susceptible Hosts
    Steven T. Denham, Morgan A. Wambaugh, Jessica C.S. Brown
    Journal of Molecular Biology.2019; 431(16): 2982.     CrossRef
  • Aspergillus fumigatus High Osmolarity Glycerol Mitogen Activated Protein Kinases SakA and MpkC Physically Interact During Osmotic and Cell Wall Stresses
    Adriana Oliveira Manfiolli, Eliciane Cevolani Mattos, Leandro José de Assis, Lilian Pereira Silva, Mevlüt Ulaş, Neil Andrew Brown, Rafael Silva-Rocha, Özgür Bayram, Gustavo H. Goldman
    Frontiers in Microbiology.2019;[Epub]     CrossRef
  • Characterizing the Pathogenic, Genomic, and Chemical Traits of Aspergillus fischeri , a Close Relative of the Major Human Fungal Pathogen Aspergillus fumigatus
    Matthew E. Mead, Sonja L. Knowles, Huzefa A. Raja, Sarah R. Beattie, Caitlin H. Kowalski, Jacob L. Steenwyk, Lilian P. Silva, Jessica Chiaratto, Laure N. A. Ries, Gustavo H. Goldman, Robert A. Cramer, Nicholas H. Oberlies, Antonis Rokas, Aaron P. Mitchell
    mSphere.2019;[Epub]     CrossRef
  • Aspergillus fumigatus phosphoethanolamine transferase gene gpi7 is required for proper transportation of the cell wall GPI-anchored proteins and polarized growth
    Haomiao Ouyang, Ting Du, Hui Zhou, Iain B. H. Wilson, Jinghua Yang, Jean-Paul Latgé, Cheng Jin
    Scientific Reports.2019;[Epub]     CrossRef
  • Overview of selected virulence attributes in Aspergillus fumigatus, Candida albicans, Cryptococcus neoformans, Trichophyton rubrum, and Exophiala dermatitidis
    Hazal Boral, Banu Metin, Aylin Döğen, Seyedmojtaba Seyedmousavi, Macit Ilkit
    Fungal Genetics and Biology.2018; 111: 92.     CrossRef
  • Heavy Metal-Induced Expression of PcaA Provides Cadmium Tolerance to Aspergillus fumigatus and Supports Its Virulence in the Galleria mellonella Model
    Fruzsina Bakti, Christoph Sasse, Thorsten Heinekamp, István Pócsi, Gerhard H. Braus
    Frontiers in Microbiology.2018;[Epub]     CrossRef
  • Predicted Glycerol 3-Phosphate Dehydrogenase Homologs and the Glycerol Kinase GlcA Coordinately Adapt to Various Carbon Sources and Osmotic Stress in Aspergillus fumigatus
    Chi Zhang, Xiuhua Meng, Huiyu Gu, Zhihua Ma, Ling Lu
    G3 Genes|Genomes|Genetics.2018; 8(7): 2291.     CrossRef
  • Heterogeneity in Pathogenicity-related Properties and Stress Tolerance in Aspergillus fumigatus Clinical Isolates
    Daisuke Hagiwara, Hiroki Takahashi, Hiroshi Takagi, Akira Watanabe, Katsuhiko Kamei
    Medical Mycology Journal.2018; 59(4): E63.     CrossRef
  • Additional oxidative stress reroutes the global response of Aspergillus fumigatus to iron depletion
    Vivien Kurucz, Thomas Krüger, Károly Antal, Anna-Maria Dietl, Hubertus Haas, István Pócsi, Olaf Kniemeyer, Tamás Emri
    BMC Genomics.2018;[Epub]     CrossRef
  • Fungal G-protein-coupled receptors: mediators of pathogenesis and targets for disease control
    Neil Andrew Brown, Sanne Schrevens, Patrick van Dijck, Gustavo Henrique Goldman
    Nature Microbiology.2018; 3(4): 402.     CrossRef
  • Dynamic Fungal Cell Wall Architecture in Stress Adaptation and Immune Evasion
    Alex Hopke, Alistair J.P. Brown, Rebecca A. Hall, Robert T. Wheeler
    Trends in Microbiology.2018; 26(4): 284.     CrossRef
  • A cytosine methyltransferase ortholog dmtA is involved in the sensitivity of Aspergillus flavus to environmental stresses
    Qing-Qing Zhi, Jie-Ying Li, Qiu-Yun Liu, Zhu-Mei He
    Fungal Biology.2017; 121(5): 501.     CrossRef
  • Global gene expression reveals stress-responsive genes in Aspergillus fumigatus mycelia
    Hiroki Takahashi, Yoko Kusuya, Daisuke Hagiwara, Azusa Takahashi-Nakaguchi, Kanae Sakai, Tohru Gonoi
    BMC Genomics.2017;[Epub]     CrossRef
  • The putative flavin carrier family FlcA-C is important forAspergillus fumigatusvirulence
    Patrícia A. de Castro, Jéssica Chiaratto, Enyara Rezende Morais, Thaila Fernanda dos Reis, Thomas K. Mitchell, Neil A. Brown, Gustavo H. Goldman
    Virulence.2017; 8(6): 797.     CrossRef
  • Transcriptome-Based Modeling Reveals that Oxidative Stress Induces Modulation of the AtfA-Dependent Signaling Networks inAspergillus nidulans
    Erzsébet Orosz, Károly Antal, Zoltán Gazdag, Zsuzsa Szabó, Kap-Hoon Han, Jae-Hyuk Yu, István Pócsi, Tamás Emri
    International Journal of Genomics.2017; 2017: 1.     CrossRef
  • Genome-wide transcriptome analysis ofAspergillus fumigatusexposed to osmotic stress reveals regulators of osmotic and cell wall stresses that are SakAHOG1and MpkC dependent
    Lilian Pereira Silva, Patrícia Alves de Castro, Thaila Fernanda dos Reis, Mario Henrique Paziani, Márcia Regina Von Zeska Kress, Diego M. Riaño-Pachón, Daisuke Hagiwara, Laure N. A. Ries, Neil Andrew Brown, Gustavo H. Goldman
    Cellular Microbiology.2017; 19(4): e12681.     CrossRef
  • Aspergillus fumigatus morphology and dynamic host interactions
    Frank L. van de Veerdonk, Mark S. Gresnigt, Luigina Romani, Mihai G. Netea, Jean-Paul Latgé
    Nature Reviews Microbiology.2017; 15(11): 661.     CrossRef
  • Human fungal pathogens: Why should we learn?
    Jeong-Yoon Kim
    Journal of Microbiology.2016; 54(3): 145.     CrossRef
  • Mitogen activated protein kinases SakAHOG1 and MpkC collaborate for Aspergillus fumigatus virulence
    Ariane Cristina Mendes de Oliveira Bruder Nascimento, Thaila Fernanda dos Reis, Patrícia Alves de Castro, Juliana I. Hori, Vinícius Leite Pedro Bom, Leandro José de Assis, Leandra Naira Zambelli Ramalho, Marina Campos Rocha, Iran Malavazi, Neil Andrew Bro
    Molecular Microbiology.2016; 100(5): 841.     CrossRef
  • Proteomic analysis of Aspergillus fumigatus – clinical implications
    Nicola M. Moloney, Rebecca A. Owens, Sean Doyle
    Expert Review of Proteomics.2016; 13(7): 635.     CrossRef
  • Aspergillus fumigatusMADS-Box Transcription FactorrlmAIs Required for Regulation of the Cell Wall Integrity and Virulence
    Marina Campos Rocha, João Henrique Tadini Marilhano Fabri, Krissia Franco de Godoy, Patrícia Alves de Castro, Juliana Issa Hori, Anderson Ferreira da Cunha, Mark Arentshorst, Arthur F J Ram, Cees A M J J van den Hondel, Gustavo Henrique Goldman, Iran Mala
    G3 Genes|Genomes|Genetics.2016; 6(9): 2983.     CrossRef
  • Transcriptional Control of Drug Resistance, Virulence and Immune System Evasion in Pathogenic Fungi: A Cross-Species Comparison
    Pedro Pais, Catarina Costa, Mafalda Cavalheiro, Daniela Romão, Miguel C. Teixeira
    Frontiers in Cellular and Infection Microbiology.2016;[Epub]     CrossRef
  • How to invade a susceptible host: cellular aspects of aspergillosis
    Sven Krappmann
    Current Opinion in Microbiology.2016; 34: 136.     CrossRef
  • Epidemiological and Genomic Landscape of Azole Resistance Mechanisms in Aspergillus Fungi
    Daisuke Hagiwara, Akira Watanabe, Katsuhiko Kamei, Gustavo H. Goldman
    Frontiers in Microbiology.2016;[Epub]     CrossRef
  • Aspergillosis and stem cell transplantation: An overview of experimental pathogenesis studies
    Nadia Al-Bader, Donald C. Sheppard
    Virulence.2016; 7(8): 950.     CrossRef
MINIREVIEW] Regulation of Escherichia coli RNase III activity
Boram Lim , Minji Sim , Howoon Lee , Seogang Hyun , Younghoon Lee , Yoonsoo Hahn , Eunkyoung Shin , Kangseok Lee
J. Microbiol. 2015;53(8):487-494.   Published online July 31, 2015
DOI: https://doi.org/10.1007/s12275-015-5323-x
  • 80 View
  • 0 Download
  • 12 Crossref
AbstractAbstract
Bacterial cells respond to changes in the environment by adjusting their physiological reactions. In cascades of cellular responses to stresses of various origins, rapid modulation of RNA function is known to be an effective biochemical adaptation. Among many factors affecting RNA function, RNase III, a member of the phylogenetically highly conserved endoribonuclease III family, plays a key role in posttranscriptional regulatory pathways in Escherichia coli. In this review, we provide an overview of the factors affecting RNase III activity in E. coli.

Citations

Citations to this article as recorded by  
  • Comparative Transcriptomic Analysis of Flagellar-Associated Genes in Salmonella Typhimurium and Its rnc Mutant
    Seungmok Han, Ji-Won Byun, Minho Lee
    Journal of Microbiology.2024; 62(1): 33.     CrossRef
  • arfAantisense RNA regulates MscL excretory activity
    Rosa Morra, Fenryco Pratama, Thomas Butterfield, Geizecler Tomazetto, Kate Young, Ruth Lopez, Neil Dixon
    Life Science Alliance.2023; 6(6): e202301954.     CrossRef
  • Transcriptome and metabolome analyses of response of Synechocystis sp. PCC 6803 to methyl viologen
    Xinyu Hu, Tianyuan Zhang, Kai Ji, Ke Luo, Li Wang, Wenli Chen
    Applied Microbiology and Biotechnology.2021; 105(21-22): 8377.     CrossRef
  • Endoribonuclease-mediated control of hns mRNA stability constitutes a key regulatory pathway for Salmonella Typhimurium pathogenicity island 1 expression
    Minho Lee, Minkyung Ryu, Minju Joo, Young-Jin Seo, Jaejin Lee, Hong-Man Kim, Eunkyoung Shin, Ji-Hyun Yeom, Yong-Hak Kim, Jeehyeon Bae, Kangseok Lee, William Navarre
    PLOS Pathogens.2021; 17(2): e1009263.     CrossRef
  • Trans-acting regulators of ribonuclease activity
    Jaejin Lee, Minho Lee, Kangseok Lee
    Journal of Microbiology.2021; 59(4): 341.     CrossRef
  • RNase III, Ribosome Biogenesis and Beyond
    Maxence Lejars, Asaki Kobayashi, Eliane Hajnsdorf
    Microorganisms.2021; 9(12): 2608.     CrossRef
  • The rnc Gene Regulates the Microstructure of Exopolysaccharide in the Biofilm of Streptococcus mutans through the β-Monosaccharides
    Yangyu Lu, Hongyu Zhang, Meng Li, Mengying Mao, Jiaqi Song, Yalan Deng, Lei Lei, Yingming Yang, Tao Hu
    Caries Research.2021; 55(5): 534.     CrossRef
  • Distributive enzyme binding controlled by local RNA context results in 3′ to 5′ directional processing of dicistronic tRNA precursors byEscherichia coliribonuclease P
    Jing Zhao, Michael E Harris
    Nucleic Acids Research.2019; 47(3): 1451.     CrossRef
  • RNase G controls tpiA mRNA abundance in response to oxygen availability in Escherichia coli
    Jaejin Lee, Dong-Ho Lee, Che Ok Jeon, Kangseok Lee
    Journal of Microbiology.2019; 57(10): 910.     CrossRef
  • The coordinated action of RNase III and RNase G controls enolase expression in response to oxygen availability in Escherichia coli
    Minho Lee, Minju Joo, Minji Sim, Se-Hoon Sim, Hyun-Lee Kim, Jaejin Lee, Minkyung Ryu, Ji-Hyun Yeom, Yoonsoo Hahn, Nam-Chul Ha, Jang-Cheon Cho, Kangseok Lee
    Scientific Reports.2019;[Epub]     CrossRef
  • Identification of endoribonuclease specific cleavage positions reveals novel targets of RNase III inStreptococcus pyogenes
    Anaïs Le Rhun, Anne-Laure Lécrivain, Johan Reimegård, Estelle Proux-Wéra, Laura Broglia, Cristina Della Beffa, Emmanuelle Charpentier
    Nucleic Acids Research.2017; : gkw1316.     CrossRef
  • Regulation and functions of bacterial PNPase
    Federica Briani, Thomas Carzaniga, Gianni Dehò
    WIREs RNA.2016; 7(2): 241.     CrossRef
Research Support, Non-U.S. Gov't
Identification of [sigma]^B-Dependent Promoters Using Consensus-Directed Search of Streptomyces coelicolor Genome
Eun-Jin Lee , You-Hee Cho , Hyo-Sub Kim , Jung-Hye Roe
J. Microbiol. 2004;42(2):147-151.
DOI: https://doi.org/2030 [pii]
  • 35 View
  • 0 Download
AbstractAbstract
[sigma]^B plays an important role in both osmoprotection and proper differentiation in Streptomyces coelicolor A3(2). We searched for candidate members of the [sigma]^B regulon from the genome database, using the consensus promoter sequence (GNNTN_14-16GGGTAC/T). The list consists of 115 genes, and includes all the known [sigma]^B target genes and many other genes whose functions are related to stress protection and differentiation.

Journal of Microbiology : Journal of Microbiology
TOP