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clpC操纵子调控炭疽芽孢杆菌的细胞结构和孢子形成。

clpC operon regulates cell architecture and sporulation in Bacillus anthracis.

作者信息

Singh Lalit K, Dhasmana Neha, Sajid Andaleeb, Kumar Prasun, Bhaduri Asani, Bharadwaj Mitasha, Gandotra Sheetal, Kalia Vipin C, Das Taposh K, Goel Ajay K, Pomerantsev Andrei P, Misra Richa, Gerth Ulf, Leppla Stephen H, Singh Yogendra

机构信息

CSIR-Institute of Genomics and Integrative Biology, Delhi, 110007, India.

出版信息

Environ Microbiol. 2015 Mar;17(3):855-65. doi: 10.1111/1462-2920.12548. Epub 2014 Jul 17.

Abstract

The clpC operon is known to regulate several processes such as genetic competence, protein degradation and stress survival in bacteria. Here, we describe the role of clpC operon in Bacillus anthracis. We generated knockout strains of the clpC operon genes to investigate the impact of CtsR, McsA, McsB and ClpC deletion on essential processes of B. anthracis. We observed that growth, cell division, sporulation and germination were severely affected in mcsB and clpC deleted strains, while none of deletions affected toxin secretion. Growth defect in these strains was pronounced at elevated temperature. The growth pattern gets restored on complementation of mcsB and clpC in respective mutants. Electron microscopic examination revealed that mcsB and clpC deletion also causes defect in septum formation leading to cell elongation. These vegetative cell deformities were accompanied by inability of mutant strains to generate morphologically intact spores. Higher levels of polyhydroxybutyrate granules accumulation were also observed in these deletion strains, indicating a defect in sporulation process. Our results demonstrate, for the first time, the vital role played by McsB and ClpC in physiology of B. anthracis and open up further interest on this operon, which might be of importance to success of B. anthracis as pathogen.

摘要

已知clpC操纵子可调节细菌中的多种过程,如遗传感受态、蛋白质降解和应激存活。在此,我们描述了clpC操纵子在炭疽芽孢杆菌中的作用。我们构建了clpC操纵子基因的敲除菌株,以研究CtsR、McsA、McsB和ClpC缺失对炭疽芽孢杆菌基本过程的影响。我们观察到,在缺失mcsB和clpC的菌株中,生长、细胞分裂、孢子形成和萌发受到严重影响,而所有缺失均未影响毒素分泌。这些菌株在高温下生长缺陷明显。在各自的突变体中对mcsB和clpC进行互补后,生长模式得以恢复。电子显微镜检查显示,mcsB和clpC的缺失还导致隔膜形成缺陷,从而导致细胞伸长。这些营养细胞畸形伴随着突变菌株无法产生形态完整的孢子。在这些缺失菌株中还观察到更高水平的聚羟基丁酸酯颗粒积累,表明孢子形成过程存在缺陷。我们的结果首次证明了McsB和ClpC在炭疽芽孢杆菌生理学中所起的重要作用,并引发了对该操纵子的进一步关注,这可能对炭疽芽孢杆菌作为病原体的成功至关重要。

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