Characterization of two membrane-associated protease genes obtained from screening out-membrane protein genes of Flavobacterium columnare G(4)
文献类型:期刊论文
作者 | Xie, HX; Nie, P; Sun, BJ |
刊名 | JOURNAL OF FISH DISEASES
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出版日期 | 2004-12-01 |
卷号 | 27期号:12页码:719-729 |
关键词 | Flavobacterium columnare G(4) gene cloning library screening membrane-associated zinc metalloprotease prolyl oligopeptidase outer membrane protein |
ISSN号 | 0140-7775 |
通讯作者 | Nie, P, Chinese Acad Sci, Inst Hydrobiol, State Key Lab Freshwater Ecol & Biotechnol, Wuhan 430072, Hubei Province, Peoples R China |
中文摘要 | In order to identify genes encoding the outer membrane proteins (OMPs) of the myxobacter Flavobacterium columnare G(4), the expression library of the bacterium was screened by using rabbit antisera developed against its OMPs. Positive colonies of Escherichia coli M15 containing fragments encoding the bacterial OMPs were selected for cloning the relevant genes by genomic walking methods. Two genes encoding a membrane-associated zinc metalloprotease and prolyl oligopeptidase are reported in this paper. The membrane-associated zinc metalloprotease gene (map) is 1800 bp in length, coding for 449 amino acids (aa). Despite the presence of a conserved motif HEXXH for all metalloproteases, the special HEXXH similar to 32 aa similar to E motif of the F. columnare G(4) Map and its low level of identity with other reported zinc-containing metalloproteases may imply that the membrane-associated zinc metalloprotease of F. columnare G(4) represents a new family of zincins. The gene encoding prolyl oligopeptidase (Pop), a serine proteinase, is 2352 bp in length, coding for 649 aa. Sequence homology analysis revealed that the Pop is also novel as it has <50% identity with other reported prolyl oligopeptidase family proteins. The present study represents the first to employ anti-fish bacterial OMP sera to screen genes of membrane-associated proteases of fish pathogenic bacteria, and to provide necessary information for the examination of the role of the two genes in the infection and pathogenesis of F. columnare. |
英文摘要 | In order to identify genes encoding the outer membrane proteins (OMPs) of the myxobacter Flavobacterium columnare G(4), the expression library of the bacterium was screened by using rabbit antisera developed against its OMPs. Positive colonies of Escherichia coli M15 containing fragments encoding the bacterial OMPs were selected for cloning the relevant genes by genomic walking methods. Two genes encoding a membrane-associated zinc metalloprotease and prolyl oligopeptidase are reported in this paper. The membrane-associated zinc metalloprotease gene (map) is 1800 bp in length, coding for 449 amino acids (aa). Despite the presence of a conserved motif HEXXH for all metalloproteases, the special HEXXH similar to 32 aa similar to E motif of the F. columnare G(4) Map and its low level of identity with other reported zinc-containing metalloproteases may imply that the membrane-associated zinc metalloprotease of F. columnare G(4) represents a new family of zincins. The gene encoding prolyl oligopeptidase (Pop), a serine proteinase, is 2352 bp in length, coding for 649 aa. Sequence homology analysis revealed that the Pop is also novel as it has <50% identity with other reported prolyl oligopeptidase family proteins. The present study represents the first to employ anti-fish bacterial OMP sera to screen genes of membrane-associated proteases of fish pathogenic bacteria, and to provide necessary information for the examination of the role of the two genes in the infection and pathogenesis of F. columnare. |
WOS标题词 | Science & Technology ; Life Sciences & Biomedicine |
学科主题 | Fisheries; Marine & Freshwater Biology; Veterinary Sciences |
类目[WOS] | Fisheries ; Marine & Freshwater Biology ; Veterinary Sciences |
研究领域[WOS] | Fisheries ; Marine & Freshwater Biology ; Veterinary Sciences |
关键词[WOS] | PROLYL ENDOPEPTIDASE ; AEROMONAS-SALMONICIDA ; FLEXIBACTER-COLUMNARIS ; PROTECTIVE IMMUNITY ; ATLANTIC SALMON ; RAINBOW-TROUT ; PDZ DOMAINS ; ENZYME GENE ; GILL TISSUE ; CLONING |
收录类别 | SCI |
语种 | 英语 |
WOS记录号 | WOS:000225487200006 |
公开日期 | 2010-10-13 |
源URL | [http://ir.ihb.ac.cn/handle/152342/9374] ![]() |
专题 | 水生生物研究所_中科院水生所知识产出(2009年前)_期刊论文 |
作者单位 | 1.Chinese Acad Sci, Inst Hydrobiol, State Key Lab Freshwater Ecol & Biotechnol, Wuhan 430072, Hubei Province, Peoples R China 2.Chinese Acad Sci, Inst Hydrobiol, Lab Fish Dis, Wuhan 430072, Hubei Province, Peoples R China |
推荐引用方式 GB/T 7714 | Xie, HX,Nie, P,Sun, BJ. Characterization of two membrane-associated protease genes obtained from screening out-membrane protein genes of Flavobacterium columnare G(4)[J]. JOURNAL OF FISH DISEASES,2004,27(12):719-729. |
APA | Xie, HX,Nie, P,&Sun, BJ.(2004).Characterization of two membrane-associated protease genes obtained from screening out-membrane protein genes of Flavobacterium columnare G(4).JOURNAL OF FISH DISEASES,27(12),719-729. |
MLA | Xie, HX,et al."Characterization of two membrane-associated protease genes obtained from screening out-membrane protein genes of Flavobacterium columnare G(4)".JOURNAL OF FISH DISEASES 27.12(2004):719-729. |
入库方式: OAI收割
来源:水生生物研究所
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