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Analysis of Bacillus subtilis sporulation with spore-converting bacteriophage PMB12.用孢子转化噬菌体PMB12分析枯草芽孢杆菌的孢子形成
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Nucleotide sequence of the spo0B gene of Bacillus subtilis and regulation of its expression.枯草芽孢杆菌spo0B基因的核苷酸序列及其表达调控
Proc Natl Acad Sci U S A. 1984 Nov;81(22):7012-6. doi: 10.1073/pnas.81.22.7012.
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Use of a lacZ fusion to study the role of the spoO genes of Bacillus subtilis in developmental regulation.利用lacZ融合技术研究枯草芽孢杆菌spoO基因在发育调控中的作用。
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The stability of messenger ribonucleic acid during sporulation in Bacillus subtilis.枯草芽孢杆菌孢子形成过程中信使核糖核酸的稳定性
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5
Chromosomal location of genes regulating resistance to bacteriophage in Bacillus subtilis.枯草芽孢杆菌中调控噬菌体抗性的基因的染色体定位。
J Bacteriol. 1969 Jun;98(3):1087-97. doi: 10.1128/jb.98.3.1087-1097.1969.
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Development of competence in the Bacillus subtilis transformation system.枯草芽孢杆菌转化系统能力的发展
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Catabolic repression of bacterial sporulation.细菌芽孢形成的分解代谢阻遏
Proc Natl Acad Sci U S A. 1965 Sep;54(3):704-11. doi: 10.1073/pnas.54.3.704.
8
Statistical estimate of the total number of operons specific for Bacillus subtilis sporulation.枯草芽孢杆菌孢子形成特有的操纵子总数的统计估计。
J Bacteriol. 1974 Sep;119(3):684-90. doi: 10.1128/jb.119.3.684-690.1974.
9
Catabolite-resistant sporulation (crsA) mutations in the Bacillus subtilis RNA polymerase sigma 43 gene (rpoD) can suppress and be suppressed by mutations in spo0 genes.枯草芽孢杆菌RNA聚合酶σ43基因(rpoD)中的抗分解代谢物芽孢形成(crsA)突变可被spo0基因突变抑制,同时也能抑制spo0基因突变。
Proc Natl Acad Sci U S A. 1985 Dec;82(23):8124-8. doi: 10.1073/pnas.82.23.8124.
10
Sequence analysis of the spo0B locus reveals a polycistronic transcription unit.spo0B基因座的序列分析揭示了一个多顺反子转录单元。
J Bacteriol. 1985 Feb;161(2):556-62. doi: 10.1128/jb.161.2.556-562.1985.

枯草芽孢杆菌spo0J基因:参与孢子形成的分解代谢物阻遏的证据。

The Bacillus subtilis spo0J gene: evidence for involvement in catabolite repression of sporulation.

作者信息

Mysliwiec T H, Errington J, Vaidya A B, Bramucci M G

机构信息

Department of Microbiology and Immunology, Hahnemann University, Philadelphia, Pennsylvania 19102-1192.

出版信息

J Bacteriol. 1991 Mar;173(6):1911-9. doi: 10.1128/jb.173.6.1911-1919.1991.

DOI:10.1128/jb.173.6.1911-1919.1991
PMID:1900505
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC207721/
Abstract

Previous observations concerning the ability of the Bacillus subtilis bacteriophages SP10 and PMB12 to suppress mutations in spo0J and to make wild-type sporulation catabolite resistant suggested that spo0J had a role in catabolite repression of sporulation. This suggestion was supported in the present report by the ability of the catabolite-resistant sporulation mutation crsF4 to suppress a Tn917 insertion mutation of the B. subtilis spo0J locus (spo0J::Tn917 omega HU261) in medium without glucose. Although crsF4 and SP10 made wild-type B. subtilis sporulation catabolite resistant, neither crsF4 nor SP10 caused a mutant with spo0J::Tn917 omega HU261 to sporulate in medium with glucose. Sequencing the spo0J locus revealed an open reading frame that was 179 codons in length. Disruption of the open reading frame resulted in a sporulation-negative (Spo-) phenotype that was similar to those of other spo0J mutations. Analysis of the deduced amino acid sequence of the spo0J locus indicated that the spo0J gene product contains an alpha-helix-turn-alpha-helix unit similar to the motif found in lambda Cro-like DNA-binding proteins.

摘要

先前关于枯草芽孢杆菌噬菌体SP10和PMB12抑制spo0J基因突变以及使野生型孢子形成对分解代谢物产生抗性的观察结果表明,spo0J在孢子形成的分解代谢物阻遏中发挥作用。本报告支持了这一观点,即分解代谢物抗性孢子形成突变体crsF4能够在不含葡萄糖的培养基中抑制枯草芽孢杆菌spo0J基因座(spo0J::Tn917 omega HU261)的Tn917插入突变。尽管crsF4和SP10使野生型枯草芽孢杆菌的孢子形成对分解代谢物产生抗性,但在含有葡萄糖的培养基中,crsF4和SP10均不能使具有spo0J::Tn917 omega HU261的突变体形成孢子。对spo0J基因座进行测序,发现了一个长度为179个密码子的开放阅读框。破坏该开放阅读框会导致孢子形成阴性(Spo-)表型,这与其他spo0J突变的表型相似。对spo0J基因座推导的氨基酸序列进行分析表明,spo0J基因产物包含一个α-螺旋-转角-α-螺旋单元,类似于在λ Cro样DNA结合蛋白中发现的基序。