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本文引用的文献

1
Evaluation of normalization reference genes for RT-qPCR analysis of spo0A and four sporulation sigma factor genes in Clostridium botulinum Group I strain ATCC 3502.评估用于 I 组肉毒梭菌 ATCC 3502 菌株 spo0A 和四个孢子形成σ因子基因 RT-qPCR 分析的标准化参考基因。
Anaerobe. 2014 Apr;26:14-9. doi: 10.1016/j.anaerobe.2013.12.003. Epub 2014 Jan 2.
2
σK of Clostridium acetobutylicum is the first known sporulation-specific sigma factor with two developmentally separated roles, one early and one late in sporulation.丙酮丁醇梭菌的 σK 是第一个已知的具有两个发育分离作用的孢子形成特异性 σ 因子,一个在孢子形成的早期,另一个在晚期。
J Bacteriol. 2014 Jan;196(2):287-99. doi: 10.1128/JB.01103-13. Epub 2013 Nov 1.
3
The spore differentiation pathway in the enteric pathogen Clostridium difficile.肠道病原体艰难梭菌中的孢子分化途径。
PLoS Genet. 2013;9(10):e1003782. doi: 10.1371/journal.pgen.1003782. Epub 2013 Oct 3.
4
Genome-wide analysis of cell type-specific gene transcription during spore formation in Clostridium difficile.艰难梭菌孢子形成过程中细胞类型特异性基因转录的全基因组分析。
PLoS Genet. 2013;9(10):e1003756. doi: 10.1371/journal.pgen.1003756. Epub 2013 Oct 3.
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Global analysis of the sporulation pathway of Clostridium difficile.艰难梭菌孢子形成途径的全局分析。
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6
Alternative sigma factor SigK has a role in stress tolerance of group I Clostridium botulinum strain ATCC 3502.替代 sigma 因子 SigK 在 I 组肉毒梭菌菌株 ATCC 3502 的应激耐受中起作用。
Appl Environ Microbiol. 2013 Jun;79(12):3867-9. doi: 10.1128/AEM.04036-12. Epub 2013 Apr 5.
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Ultrasensitivity of the Bacillus subtilis sporulation decision.枯草芽孢杆菌孢子形成决策的超敏性。
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ClosTron-mediated engineering of Clostridium.Clostridium 的 Clostron 介导工程改造
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Primer3--new capabilities and interfaces.Primer3--新功能和界面。
Nucleic Acids Res. 2012 Aug;40(15):e115. doi: 10.1093/nar/gks596. Epub 2012 Jun 22.
10
Involvement of Clostridium botulinum ATCC 3502 sigma factor K in early-stage sporulation.参与型肉毒梭菌 ATCC 3502σ因子 K 在早期孢子形成中的作用。
Appl Environ Microbiol. 2012 Jul;78(13):4590-6. doi: 10.1128/AEM.00304-12. Epub 2012 Apr 27.

替代西格玛因子SigF、SigE和SigG对于肉毒梭菌ATCC 3502的孢子形成至关重要。

Alternative sigma factors SigF, SigE, and SigG are essential for sporulation in Clostridium botulinum ATCC 3502.

作者信息

Kirk David G, Zhang Zhen, Korkeala Hannu, Lindström Miia

机构信息

Department of Food Hygiene and Environmental Health, Centre of Excellence in Microbial Food Safety Research, Faculty of Veterinary Medicine, University of Helsinki, Helsinki, Finland.

Department of Food Hygiene and Environmental Health, Centre of Excellence in Microbial Food Safety Research, Faculty of Veterinary Medicine, University of Helsinki, Helsinki, Finland

出版信息

Appl Environ Microbiol. 2014 Aug;80(16):5141-50. doi: 10.1128/AEM.01015-14. Epub 2014 Jun 13.

DOI:10.1128/AEM.01015-14
PMID:24928875
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4135750/
Abstract

Clostridium botulinum produces heat-resistant endospores that may germinate and outgrow into neurotoxic cultures in foods. Sporulation is regulated by the transcription factor Spo0A and the alternative sigma factors SigF, SigE, SigG, and SigK in most spore formers studied to date. We constructed mutants of sigF, sigE, and sigG in C. botulinum ATCC 3502 and used quantitative reverse transcriptase PCR and electron microscopy to assess their expression of the sporulation pathway on transcriptional and morphological levels. In all three mutants the expression of spo0A was disrupted. The sigF and sigE mutants failed to induce sigG and sigK beyond exponential-phase levels and halted sporulation during asymmetric cell division. In the sigG mutant, peak transcription of sigE was delayed and sigK levels remained lower than that in the parent strain. The sigG mutant forespore was engulfed by the mother cell and possessed a spore coat but no peptidoglycan cortex. The findings suggest that SigF and SigE of C. botulinum ATCC 3502 are essential for early sporulation and late-stage induction of sigK, whereas SigG is essential for spore cortex formation but not for coat formation, as opposed to previous observations in B. subtilis sigG mutants. Our findings add to a growing body of evidence that regulation of sporulation in C. botulinum ATCC 3502, and among the clostridia, differs from the B. subtilis model.

摘要

肉毒梭菌可产生耐热性芽孢,这些芽孢可能在食物中萌发并生长为产生神经毒素的培养物。在迄今为止研究的大多数产芽孢菌中,芽孢形成受转录因子Spo0A以及替代σ因子SigF、SigE、SigG和SigK调控。我们构建了肉毒梭菌ATCC 3502中sigF、sigE和sigG的突变体,并使用定量逆转录聚合酶链反应和电子显微镜在转录和形态水平上评估它们芽孢形成途径的表达。在所有三个突变体中,spo0A的表达均被破坏。sigF和sigE突变体在指数期水平之后无法诱导sigG和sigK,并且在不对称细胞分裂期间停止芽孢形成。在sigG突变体中,sigE的转录峰值延迟,并且sigK水平低于亲本菌株。sigG突变体的前芽孢被母细胞吞噬,并且具有芽孢衣但没有肽聚糖皮层。这些发现表明,肉毒梭菌ATCC 3502的SigF和SigE对于早期芽孢形成和sigK的后期诱导至关重要,而SigG对于芽孢皮层形成至关重要,但对于芽孢衣形成并非如此,这与先前在枯草芽孢杆菌sigG突变体中的观察结果相反。我们的发现增加了越来越多的证据,表明肉毒梭菌ATCC 3502以及梭菌属中的芽孢形成调控与枯草芽孢杆菌模型不同。