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Activation of the SigE-SigB signaling pathway by inhibition of the respiratory electron transport chain and its effect on rifampicin resistance in Mycobacterium smegmatis
Yuna Oh , Hye-In Lee , Ji-A Jeong , Seonghan Kim , Jeong-Il Oh
J. Microbiol. 2022;60(9):935-947.   Published online August 1, 2022
DOI: https://doi.org/10.1007/s12275-022-2202-0
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AbstractAbstract
Using a mutant of Mycobacterium smegmatis lacking the major aa3 cytochrome c oxidase of the electron transport chain (Δaa3), we demonstrated that inhibition of the respiratory electron transport chain led to an increase in antibiotic resistance of M. smegmatis to isoniazid, rifampicin, ethambutol, and tetracycline. The alternative sigma factors SigB and SigE were shown to be involved in an increase in rifampicin resistance of M. smegmatis induced under respiration-inhibitory conditions. As in Mycobacterium tuberculosis, SigE and SigB form a hierarchical regulatory pathway in M. smegmatis through SigE-dependent transcription of sigB. Expression of sigB and sigE was demonstrated to increase in the Δaa3 mutant, leading to upregulation of the SigB-dependent genes in the mutant. The phoU2 (MSMEG_1605) gene implicated in a phosphatesignaling pathway and the MSMEG_1097 gene encoding a putative glycosyltransferase were identified to be involved in the SigB-dependent enhancement of rifampicin resistance observed for the Δaa3 mutant of M. smegmatis. The significance of this study is that the direct link between the functionality of the respiratory electron transport chain and antibiotic resistance in mycobacteria was demonstrated for the first time using an electron transport chain mutant rather than inhibitors of electron transport chain.

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  • Rel-dependent decrease in the expression of ribosomal protein genes by inhibition of the respiratory electron transport chain in Mycobacterium smegmatis
    Na-Kyeong Kim, Jong-Eun Baek, Ye-Jin Lee, Yuna Oh, Jeong-Il Oh
    Frontiers in Microbiology.2024;[Epub]     CrossRef
  • MoaB2, a newly identified transcription factor, binds to σ A in Mycobacterium smegmatis
    Barbora Brezovská, Subhash Narasimhan, Michaela Šiková, Hana Šanderová, Tomáš Kovaľ, Nabajyoti Borah, Mahmoud Shoman, Debora Pospíšilová, Viola Vaňková Hausnerová, Dávid Tužinčin, Martin Černý, Jan Komárek, Martina Janoušková, Milada Kambová, Petr Halada,
    Journal of Bacteriology.2024;[Epub]     CrossRef
  • Enhanced hypoxanthine utilization for cAMP salvage synthesis efficiently by Arthrobacter sp. CCTCC 2013431 via xanthine oxidase inhibition
    Baofeng Chen, Hai Tan, Chang Li, Linbo Li, Zhonghua Zhang, Zhigang Li
    Biotechnology Letters.2024; 46(6): 1095.     CrossRef
  • Mycobacterial Regulatory Systems Involved in the Regulation of Gene Expression Under Respiration-Inhibitory Conditions
    Yuna Oh, Ha-Na Lee, Eon-Min Ko, Ji-A Jeong, Sae Woong Park, Jeong-Il Oh
    Journal of Microbiology.2023; 61(3): 297.     CrossRef
Review
MINIREVIEW] Fungi in salterns
Dawoon Chung† , Haryun Kim† , Hyun Seok Choi
J. Microbiol. 2019;57(9):717-724.   Published online August 27, 2019
DOI: https://doi.org/10.1007/s12275-019-9195-3
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AbstractAbstract
Salterns are hypersaline extreme environments with unique physicochemical properties such as a salinity gradient. Although the investigation of microbiota in salterns has focused on archaea and bacteria, diverse fungi also thrive in the brine and soil of salterns. Fungi isolated from salterns are represented by black yeasts (Hortaea werneckii, Phaeotheca triangularis, Aureobasidium pullulans, and Trimmatostroma salinum), Cladosporium, Aspergillus, and Penicillium species. Most studies on saltern-derived fungi gave attention to black yeasts and their physiological characteristics, including growth under various culture conditions. Since then, biochemical and molecular tools have been employed to explore adaptation of these fungi to salt stress. Genome databases of several fungi in salterns are now publicly available and being used to elucidate salt tolerance mechanisms and discover the target genes for agricultural and industrial applications. Notably, the number of enzymes and novel metabolites known to be produced by diverse saltern-derived fungi has increased significantly. Therefore, fungi in salterns are not only interesting and important subjects to study fungal biodiversity and adaptive mechanisms in extreme environments, but also valuable bioresources with potential for biotechnological applications.

Citations

Citations to this article as recorded by  
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    Ya-Li Wei, Zi-Jie Long, Zhen-Dong Li, Ming-Xun Ren
    Applied Soil Ecology.2024; 198: 105392.     CrossRef
  • Overgrowth of filamentous fungi in halophilic activated granule sludge reactivated after refrigeration: Insights into bacterial-fungal interactions
    Ji-Lin Huang, You-Wei Cui, Chen Chen
    Chemical Engineering Journal.2024; 482: 148859.     CrossRef
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    Applied Microbiology and Biotechnology.2024;[Epub]     CrossRef
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    RYO HAGIUDA, DAI HIROSE
    Journal of Microorganism Control.2024; 29(1): 17.     CrossRef
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    David L. Parrott, Bonnie K. Baxter
    Frontiers in Fungal Biology.2024;[Epub]     CrossRef
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    Jurgita Švedienė, Vita Raudonienė, Goda Mizerienė, Jolanta Rimšaitė, Sigitas Algis Davenis, Povilas Ivinskis
    Journal of Fungi.2024; 10(7): 442.     CrossRef
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    Cene Gostinčar, Nina Gunde-Cimerman
    Applied Microbiology and Biotechnology.2024;[Epub]     CrossRef
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    Monika Novak Babič, Sara Ragucci, Adrijana Leonardi, Miha Pavšič, Nicola Landi, Igor Križaj, Nina Gunde-Cimerman, Kristina Sepčić, Antimo Di Maro
    Biomolecules.2024; 14(3): 336.     CrossRef
  • Revealing the Mechanism of Aroma Production Driven by High Salt Stress in Trichomonascus ciferrii WLW
    Fangying Xian, Lin Yang, Huaqing Ye, Jinlin Xu, Xiaoping Yue, Xiaolan Wang
    Foods.2024; 13(11): 1593.     CrossRef
  • The Fungal Side of the Story: Saprotrophic- vs. Symbiotrophic-Predicted Ecological Roles of Fungal Communities in Two Meromictic Hypersaline Lakes from Romania
    Cristina Mircea, Ioana Rusu, Erika Andrea Levei, Adorján Cristea, Ionuț Mădălin Gridan, Adrian Vasile Zety, Horia Leonard Banciu
    Microbial Ecology.2024;[Epub]     CrossRef
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    Shivankar Agrawal, Pruthviraj Chavan, Laurent Dufossé
    Journal of Fungi.2024; 10(4): 290.     CrossRef
  • Multi-functional xylanase from Aspergillus sydowii : biosynthesis of nanoconjugates, optimization by Taguchi approach and biodeinking potential
    J. A. Elegbede, A. Lateef, E. B. Gueguim-Kana, L. S. Beukes, N. Matyumza
    Preparative Biochemistry & Biotechnology.2024; 54(5): 622.     CrossRef
  • Secofumitremorgins C and D, a pair of atropisomers from saltern-derived fungus Aspergillus fumigatus GXIMD00544
    Geng-Si Zhang, Hai-Yan Li, Li-Fen Liang, Chun-Qing Fu, Qin Yu, Kai Liu, Zhi-Wei Su, Dong-Mei Zhou, Cheng-Hai Gao, Xin-Ya Xu, Yong-Hong Liu
    Journal of Asian Natural Products Research.2024; 26(9): 1049.     CrossRef
  • Exploring Halobiome Resources for Developing Salt-Tolerant Crops: A Perspective Review
    Tushar Khare, Monica Jamla, Vartika Mathur, Vinay Kumar
    Journal of Plant Growth Regulation.2024; 43(7): 2137.     CrossRef
  • Updates on the classification and numbers of marine fungi
    Mark S. Calabon, E.B. Gareth Jones, Ka-Lai Pang, Mohamed A. Abdel-Wahab, Jing Jin, Bandarupalli Devadatha, Resurreccion B. Sadaba, Carlo Chris Apurillo, Kevin D. Hyde
    Botanica Marina.2023; 66(4): 213.     CrossRef
  • Isolation and characterization of halophilic and halotolerant fungi from man-made solar salterns in Pattani Province, Thailand
    Lakkhana Kanhayuwa Wingfield, Ninadia Jitprasitporn, Nureeda Che-alee, William C. Nierman
    PLOS ONE.2023; 18(2): e0281623.     CrossRef
  • A comparative study using response surface methodology and artificial neural network towards optimized production of melanin by Aureobasidium pullulans AKW
    WesamEldin I. A. Saber, Abeer A. Ghoniem, Fatimah O. Al-Otibi, Mohammed S. El-Hersh, Noha M. Eldadamony, Farid Menaa, Khaled M. Elattar
    Scientific Reports.2023;[Epub]     CrossRef
  • Fungal Diversity and Its Relationship with Environmental Factors in Coastal Sediments from Guangdong, China
    Keyue Wu, Yongchun Liu, Xinyu Liao, Xinyue Yang, Zihui Chen, Li Mo, Saiyi Zhong, Xiaoyong Zhang
    Journal of Fungi.2023; 9(1): 101.     CrossRef
  • Static magnetic field increases aerobic nitrogen removal from hypersaline wastewater in activated sludge with coexistence of fungi and bacteria
    Jun Chen, You-Wei Cui, Mei-Qi Huang, Hui-Juan Yan, Dong Li
    Bioresource Technology.2023; 382: 129194.     CrossRef
  • Marine fungi: A treasure trove of novel natural products and for biological discovery
    Frank Kempken, Mary Ann Jabra-Rizk
    PLOS Pathogens.2023; 19(9): e1011624.     CrossRef
  • They too serve who tolerate and survive: the need to study halotolerant fungi to appreciate their role in saline ecosystems
    T.S. Suryanarayanan, J.P. Ravishankar
    Fungal Biology Reviews.2023; 46: 100328.     CrossRef
  • Solar Salterns and Pollution: Valorization of Some Endemic Species as Sentinels in Ecotoxicology
    Wassim Guermazi, Neila Annabi-Trabelsi, Genuario Belmonte, Kais Guermazi, Habib Ayadi, Vincent Leignel
    Toxics.2023; 11(6): 524.     CrossRef
  • Response of the obligate halophile fungus Aspergillus loretoensis to stress salinity
    Amelia Portillo López, Sophia González Martínez, Edgar A López Landavery, Alma R Cabazos-Marín, Alejandro Sánchez González
    Journal of Microbiology & Experimentation.2023; 11(1): 26.     CrossRef
  • The Cytotoxic Properties of Extreme Fungi’s Bioactive Components—An Updated Metabolic and Omics Overview
    Attila Kiss, Farhad Hariri Akbari, Andrey Marchev, Viktor Papp, Iman Mirmazloum
    Life.2023; 13(8): 1623.     CrossRef
  • Understanding Fungi in Glacial and Hypersaline Environments
    Cene Gostinčar, Nina Gunde-Cimerman
    Annual Review of Microbiology.2023; 77(1): 89.     CrossRef
  • Potential of Halophilic Penicillium chrysogenum Isolated from Algerian Saline Soil to Produce Laccase on Olive Oil Wastes
    Zeyneb Boucherit, Sigrid Flahaut, Brahim Djoudi, Toma-Nardjes Mouas, Aicha Mechakra, Souad Ameddah
    Current Microbiology.2022;[Epub]     CrossRef
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    Si-Yao Wang, Yong Wang, Yan Li
    MycoKeys.2022; 91: 151.     CrossRef
  • Metagenomic analysis of the soil microbial composition and salt tolerance mechanism in Yuncheng Salt Lake, Shanxi Province
    Feifeng Zeng, Yonghong Zhu, Dongling Zhang, Zengqiang Zhao, Quansheng Li, Panpan Ma, Guoli Zhang, Yuan Wang, Shenjie Wu, Sandui Guo, Guoqing Sun
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    Ya-Li Wei, Zi-Jie Long, Ming-Xun Ren
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  • Culturomics remains a highly valuable methodology to obtain rare microbial diversity with putative biotechnological potential from two Portuguese salterns
    Eduarda Almeida, Maria F. Carvalho, Olga M. Lage
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    Asmaa Elsayis, Sahar W. M. Hassan, Khaled M. Ghanem, Heba Khairy
    Frontiers in Microbiology.2022;[Epub]     CrossRef
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    Irina Jiménez-Gómez, Gisell Valdés-Muñoz, Aldo Moreno-Ulloa, Yordanis Pérez-Llano, Tonatiuh Moreno-Perlín, Hortencia Silva-Jiménez, Fernando Barreto-Curiel, María del Rayo Sánchez-Carbente, Jorge Luis Folch-Mallol, Nina Gunde-Cimerman, Asunción Lago-Lestó
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    BMC Microbiology.2022;[Epub]     CrossRef
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Journal Article
Characterization of Flavobacterium aquimarinum sp. nov., a halotolerant bacterium isolated from seawater
Sylvia Kristyanto , Tuan Manh Nguyen , Dhiraj Kumar Chaudhary , Sang-Seob Lee , Jaisoo Kim
J. Microbiol. 2018;56(5):317-323.   Published online May 2, 2018
DOI: https://doi.org/10.1007/s12275-018-7454-3
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AbstractAbstract
A novel, aerobic, Gram-stain-negative, non-motile, non-spore forming, rod-shaped bacterium, designated strain Dol 15-39T, was isolated from a seawater sample near Geoje Island in the South Sea, Republic of Korea. The strain was found to be oxidase-negative and catalase-positive. The isolate was observed to grow at temperatures from 4 to 37°C, at salinities of up to 7%, and at pH levels from 6 to 9; moreover, it was not able to degrade starch, DNA, esculin, or tyrosine. Phylogenetic analysis based on 16S rRNA gene sequences showed that Dol 15-39T was most closely related to Flavobacterium jumunjinense HME7102T with a sequence similarity of 97.3%. However, the levels of DNA-DNA relatedness between Dol 15-39T and the most closely related species were much lower than 70%, confirming that they represented distinct genomic species. The genomic DNA G + C content of Dol 15-39T was calculated to be 32.6 mol%. MK-6 was the predominant respiratory quinine, while iso-C15:0 (25.0%), iso- C15:1 G (17.0%), and iso-C17:0 3-OH (10.4%) were the major cellular fatty acids. Phosphatidylethanolamine was identified as a major polar lipid, while various unidentified aminolipids and polar lipids were also detected. Based on polyphasic taxonomic data, Dol 15-39T represents a novel species of the genus Flavobacterium, for which the name F. aquimarinum sp. nov. is proposed. The type strain is accessible under the culture collection numbers (KEMB 9005-617T = JCM 31930T).

Citations

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  • Flavobacterium adhaerens sp. nov. and Flavobacterium maritimum sp. nov., two novel flavobacteria isolated from the Pearl River Estuary
    Zi-Qi Peng, Jia-Ling Li, Zi-Wen Yang, Pan-Deng Wang, Dan-Yuan Guo, Xiao-Qing Luo, Qi-Qi Deng, Qi Li, Ting-Ting She, Wen-Jun Li
    International Journal of Systematic and Evolutionary Microbiology .2024;[Epub]     CrossRef
  • Flavobacterium frigoritolerans sp. nov. and Flavobacterium shii sp. nov., isolated from glaciers on the Tibetan Plateau
    Lei-Lei Yang, Hong-Can Liu, Yu-Hua Xin, Qing Liu
    International Journal of Systematic and Evolutionary Microbiology .2023;[Epub]     CrossRef
  • Identification of Flavobacterium algoritolerans sp. nov. and Flavobacterium yafengii sp. nov., two novel members of the genus Flavobacterium
    Ce-Ce Yin, Lei-Lei Yang, Yu-Hua Xin, Jian Ye, Qing Liu
    International Journal of Systematic and Evolutionary Microbiology .2023;[Epub]     CrossRef
  • Ten Novel Species Belonging to the Genus Flavobacterium, Isolated from Freshwater Environments: F. praedii sp. nov., F. marginilacus sp. nov., F. aestivum sp. nov., F. flavigenum sp. nov., F. luteolum sp. nov., F. gelatinilyticum sp. nov., F. aquiphilum s
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Research Support, Non-U.S. Gov't
Virgibacillus xinjiangensis sp. nov., Isolated from a Salt Lake of Xin-jiang Province in China
Che Ok Jeon , Jeong Myeong Kim , Dong-Jin Park , Li-Hua Xu , Cheng-Lin Jiang , Chang-Jin Kim
J. Microbiol. 2009;47(6):705-709.   Published online February 4, 2010
DOI: https://doi.org/10.1007/s12275-009-0107-9
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AbstractAbstract
A strictly aerobic Gram-positive, moderately halophilic spore forming bacterium, designated strain SL6-1T, was isolated from a salt lake in Xin-jiang province, China. Growth of strain SL6-1T was observed at NaCl concentrations of 0~20% (w/v) (the optimum being 5~7%, w/v). The peptidoglycan type of strain SL6-1T was A1γ-meso-diaminopimelic acid and its major cellular fatty acids were iso-C14:0 and iso-C16:0 and anteiso-C15:0. The major respiratory isoprenoid quinone was MK-7 and the G+C content of the genomic DNA was 44.5 mol%. The major cellular phospholipids were phosphatidylglycerol and diphosphatidylglycerol. Phylogenetic analysis based on 16S rRNA gene sequences showed that strain SL6-1T formed a phylogenetic lineage within the genus Virgibacillus. Based on 16S rRNA gene sequence similarity, the strain was most closely related to Virgibacillus olivae E308T, Virgibacillus kekensis YIM kkny16T, Virgibacillus marismortui DSM 12325T with 97.1%, 97.1%, and 97.0% gene sequence similarities, respectively and the sequence similarities to other related taxa were less than 96.7%. The DNA relatedness values between strain SL6-1T and V. olivae E308T, V. kekensis YIM kkny16T, V. marismortui DSM 12325T were 16.7%, 51.0%, and 22.8%, respectively. On the basis of physiological, biochemical and phylogenetic properties, strain SL6-1T represents a novel species, for which the name Virgibacillus xinjiangensis sp. nov. is proposed. The type strain is SL6-1T (=KCTC 13128T =DSM 19031T).

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