作者
Mohammed Sebaihia, Michael W Peck, Nigel P Minton, Nicholas R Thomson, Matthew TG Holden, Wilfrid J Mitchell, Andrew T Carter, Stephen D Bentley, David R Mason, Lisa Crossman, Catherine J Paul, Alasdair Ivens, Marjon HJ Wells-Bennik, Ian J Davis, Ana M Cerdeño-Tárraga, Carol Churcher, Michael A Quail, Tracey Chillingworth, Theresa Feltwell, Audrey Fraser, Ian Goodhead, Zahra Hance, Kay Jagels, Natasha Larke, Mark Maddison, Sharon Moule, Karen Mungall, Halina Norbertczak, Ester Rabbinowitsch, Mandy Sanders, Mark Simmonds, Brian White, Sally Whithead, Julian Parkhill
发表日期
2007/7/1
期刊
Genome research
卷号
17
期号
7
页码范围
1082-1092
出版商
Cold Spring Harbor Lab
简介
Clostridium botulinum is a heterogeneous Gram-positive species that comprises four genetically and physiologically distinct groups of bacteria that share the ability to produce botulinum neurotoxin, the most poisonous toxin known to man, and the causative agent of botulism, a severe disease of humans and animals. We report here the complete genome sequence of a representative of Group I (proteolytic) C. botulinum (strain Hall A, ATCC 3502). The genome consists of a chromosome (3,886,916 bp) and a plasmid (16,344 bp), which carry 3650 and 19 predicted genes, respectively. Consistent with the proteolytic phenotype of this strain, the genome harbors a large number of genes encoding secreted proteases and enzymes involved in uptake and metabolism of amino acids. The genome also reveals a hitherto unknown ability of C. botulinum to degrade chitin. There is a significant lack of recently acquired DNA …
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