• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

负责胞外多糖柯烷酸产生的大肠杆菌K-12基因簇的组织。

Organization of the Escherichia coli K-12 gene cluster responsible for production of the extracellular polysaccharide colanic acid.

作者信息

Stevenson G, Andrianopoulos K, Hobbs M, Reeves P R

机构信息

Department of Microbiology, University of Sydney, New South Wales, Australia.

出版信息

J Bacteriol. 1996 Aug;178(16):4885-93. doi: 10.1128/jb.178.16.4885-4893.1996.

DOI:10.1128/jb.178.16.4885-4893.1996
PMID:8759852
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC178271/
Abstract

Colanic acid (CA) is an extracellular polysaccharide produced by most Escherichia coli strains as well as by other species of the family Enterobacteriaceae. We have determined the sequence of a 23-kb segment of the E. coli K-12 chromosome which includes the cluster of genes necessary for production of CA. The CA cluster comprises 19 genes. Two other sequenced genes (orf1.3 and galF), which are situated between the CA cluster and the O-antigen cluster, were shown to be unnecessary for CA production. The CA cluster includes genes for synthesis of GDP-L-fucose, one of the precursors of CA, and the gene for one of the enzymes in this pathway (GDP-D-mannose 4,6-dehydratase) was identified by biochemical assay. Six of the inferred proteins show sequence similarity to glycosyl transferases, and two others have sequence similarity to acetyl transferases. Another gene (wzx) is predicted to encode a protein with multiple transmembrane segments and may function in export of the CA repeat unit from the cytoplasm into the periplasm in a process analogous to O-unit export. The first three genes of the cluster are predicted to encode an outer membrane lipoprotein, a phosphatase, and an inner membrane protein with an ATP-binding domain. Since homologs of these genes are found in other extracellular polysaccharide gene clusters, they may have a common function, such as export of polysaccharide from the cell.

摘要

柯氏酸(CA)是大多数大肠杆菌菌株以及肠杆菌科其他物种产生的一种细胞外多糖。我们已经确定了大肠杆菌K-12染色体上一个23kb片段的序列,该片段包含产生CA所需的基因簇。CA基因簇由19个基因组成。位于CA基因簇和O抗原基因簇之间的另外两个已测序基因(orf1.3和galF)被证明对CA的产生是不必要的。CA基因簇包括CA前体之一GDP-L-岩藻糖合成的基因,并且通过生化分析鉴定了该途径中一种酶(GDP-D-甘露糖4,6-脱水酶)的基因。六个推断的蛋白质与糖基转移酶具有序列相似性,另外两个与乙酰转移酶具有序列相似性。另一个基因(wzx)预计编码一种具有多个跨膜区段的蛋白质,并且可能在类似于O单元输出的过程中参与将CA重复单元从细胞质输出到周质中。该基因簇的前三个基因预计编码一种外膜脂蛋白、一种磷酸酶和一种具有ATP结合结构域的内膜蛋白.由于这些基因的同源物存在于其他细胞外多糖基因簇中,它们可能具有共同功能,例如从细胞中输出多糖。

相似文献

1
Organization of the Escherichia coli K-12 gene cluster responsible for production of the extracellular polysaccharide colanic acid.负责胞外多糖柯烷酸产生的大肠杆菌K-12基因簇的组织。
J Bacteriol. 1996 Aug;178(16):4885-93. doi: 10.1128/jb.178.16.4885-4893.1996.
2
Cloning and analysis of duplicated rfbM and rfbK genes involved in the formation of GDP-mannose in Escherichia coli O9:K30 and participation of rfb genes in the synthesis of the group I K30 capsular polysaccharide.大肠杆菌O9:K30中参与GDP-甘露糖形成的重复rfbM和rfbK基因的克隆与分析以及rfb基因在I型K30荚膜多糖合成中的作用
J Bacteriol. 1994 Jun;176(11):3126-39. doi: 10.1128/jb.176.11.3126-3139.1994.
3
Structure of the O antigen of Escherichia coli K-12 and the sequence of its rfb gene cluster.大肠杆菌K-12 O抗原的结构及其rfb基因簇序列
J Bacteriol. 1994 Jul;176(13):4144-56. doi: 10.1128/jb.176.13.4144-4156.1994.
4
Identification of the fucose synthetase gene in the colanic acid gene cluster of Escherichia coli K-12.大肠杆菌K-12荚膜酸基因簇中岩藻糖合成酶基因的鉴定。
J Bacteriol. 1998 Feb;180(4):998-1001. doi: 10.1128/JB.180.4.998-1001.1998.
5
Identification, expression, and DNA sequence of the GDP-mannose biosynthesis genes encoded by the O7 rfb gene cluster of strain VW187 (Escherichia coli O7:K1).VW187菌株(大肠杆菌O7:K1)O7 rfb基因簇编码的GDP-甘露糖生物合成基因的鉴定、表达及DNA序列
J Bacteriol. 1993 Jan;175(1):148-58. doi: 10.1128/jb.175.1.148-158.1993.
6
Expression of the O9 polysaccharide of Escherichia coli: sequencing of the E. coli O9 rfb gene cluster, characterization of mannosyl transferases, and evidence for an ATP-binding cassette transport system.大肠杆菌O9多糖的表达:大肠杆菌O9 rfb基因簇的测序、甘露糖基转移酶的特性分析以及ATP结合盒转运系统的证据
J Bacteriol. 1995 Apr;177(8):2178-87. doi: 10.1128/jb.177.8.2178-2187.1995.
7
Genetic analysis of the Serratia marcescens N28b O4 antigen gene cluster.粘质沙雷氏菌N28b O4抗原基因簇的遗传分析。
J Bacteriol. 1999 Mar;181(6):1883-91. doi: 10.1128/JB.181.6.1883-1891.1999.
8
Molecular and functional analysis of genes required for expression of group IB K antigens in Escherichia coli: characterization of the his-region containing gene clusters for multiple cell-surface polysaccharides.大肠杆菌中IB族K抗原表达所需基因的分子与功能分析:多个细胞表面多糖的含组氨酸区域基因簇的特性
Mol Microbiol. 1997 Oct;26(1):145-61. doi: 10.1046/j.1365-2958.1997.5631930.x.
9
Genetic characterization of the Escherichia coli O66 antigen and functional identification of its wzy gene.大肠杆菌O66抗原的遗传特征及其wzy基因的功能鉴定。
J Microbiol. 2007 Feb;45(1):69-74.
10
Synthesis of the A-band polysaccharide sugar D-rhamnose requires Rmd and WbpW: identification of multiple AlgA homologues, WbpW and ORF488, in Pseudomonas aeruginosa.A带多糖糖D-鼠李糖的合成需要Rmd和WbpW:在铜绿假单胞菌中鉴定多个AlgA同源物、WbpW和ORF488。
Mol Microbiol. 1998 Sep;29(6):1419-34. doi: 10.1046/j.1365-2958.1998.01024.x.

引用本文的文献

1
Evolutionary responses of Escherichia coli to phage pressure: insights into mucoidy and colanic acid overexpression.大肠杆菌对噬菌体压力的进化反应:对黏液化和柯氏酸过表达的见解。
BMC Genomics. 2025 May 6;26(1):448. doi: 10.1186/s12864-025-11605-x.
2
Enterobacterial common antigen repeat-unit flippase WzxE is required for growth under acidic conditions, low temperature, and high osmotic stress conditions.肠杆菌共同抗原重复单元翻转酶WzxE是在酸性条件、低温和高渗透压胁迫条件下生长所必需的。
Appl Environ Microbiol. 2025 May 21;91(5):e0259524. doi: 10.1128/aem.02595-24. Epub 2025 Apr 10.
3
Enzyme cascades for nucleotide sugar regeneration in glycoconjugate synthesis.用于糖缀合物合成中核苷酸糖再生的酶级联反应。
Appl Microbiol Biotechnol. 2025 Feb 27;109(1):51. doi: 10.1007/s00253-025-13432-2.
4
Structure of WzxE the lipid III flippase for Enterobacterial Common Antigen polysaccharide.肠杆菌共同抗原多糖的脂质III翻转酶WzxE的结构
Open Biol. 2025 Jan;15(1):240310. doi: 10.1098/rsob.240310. Epub 2025 Jan 8.
5
The transcriptional response to low temperature is weakly conserved across the .对低温的转录反应在整个……中保守性较弱。 (你提供的原文不完整,这里只能翻译到这一步)
mSystems. 2024 Dec 17;9(12):e0078524. doi: 10.1128/msystems.00785-24. Epub 2024 Nov 26.
6
In Vivo Evolution of a Klebsiella pneumoniae Capsule Defect With wcaJ Mutation Promotes Complement-Mediated Opsonophagocytosis During Recurrent Infection.在复发性感染过程中,携带 wcaJ 突变的肺炎克雷伯菌荚膜缺陷的体内进化促进补体介导的调理吞噬作用。
J Infect Dis. 2024 Jul 25;230(1):209-220. doi: 10.1093/infdis/jiae003.
7
Construction of an engineered for effective synthesis of 2'-fucosyllactose the pathway.构建用于通过该途径有效合成2'-岩藻糖基乳糖的工程菌。
Synth Syst Biotechnol. 2024 Jan 6;9(1):108-114. doi: 10.1016/j.synbio.2024.01.001. eCollection 2024 Mar.
8
Lethal perturbation of an Escherichia coli regulatory network is triggered by a restriction-modification system's regulator and can be mitigated by excision of the cryptic prophage Rac.大肠杆菌调控网络的致命干扰是由限制修饰系统的调控因子触发的,可以通过切除隐藏的噬菌体 Rac 来减轻。
Nucleic Acids Res. 2024 Apr 12;52(6):2942-2960. doi: 10.1093/nar/gkad1234.
9
Engineering a synthetic energy-efficient formaldehyde assimilation cycle in Escherichia coli.在大肠杆菌中构建一个合成的、节能的甲醛同化循环。
Nat Commun. 2023 Dec 20;14(1):8490. doi: 10.1038/s41467-023-44247-2.
10
Structural and Genetic Identification of the O-Antigen from an Isolate, SD2019180, Representing a Novel Serogroup.结构和遗传鉴定一株分离株,SD2019180,代表一个新的血清群。
Int J Mol Sci. 2023 Oct 10;24(20):15040. doi: 10.3390/ijms242015040.

本文引用的文献

1
A role for exopolysaccharides in the protection of microorganisms from desiccation.胞外多糖在微生物抗干燥中的作用。
Appl Environ Microbiol. 1994 Feb;60(2):740-5. doi: 10.1128/aem.60.2.740-745.1994.
2
The identification, cloning and mutagenesis of a genetic locus required for lipopolysaccharide biosynthesis in Bordetella pertussis.百日咳博德特氏菌脂多糖生物合成所需遗传位点的鉴定、克隆及诱变
Mol Microbiol. 1996 Jan;19(1):37-52. doi: 10.1046/j.1365-2958.1996.354877.x.
3
Identification of the promoter region for the colanic acid polysaccharide biosynthetic genes in Escherichia coli K-12.大肠杆菌K-12中柯氏酸多糖生物合成基因启动子区域的鉴定
J Bacteriol. 1996 Jul;178(14):4273-80. doi: 10.1128/jb.178.14.4273-4280.1996.
4
C-terminal half of Salmonella enterica WbaP (RfbP) is the galactosyl-1-phosphate transferase domain catalyzing the first step of O-antigen synthesis.肠炎沙门氏菌WbaP(RfbP)的C端结构域是催化O抗原合成第一步的1-磷酸半乳糖基转移酶结构域。
J Bacteriol. 1996 May;178(9):2598-604. doi: 10.1128/jb.178.9.2598-2604.1996.
5
An O-antigen processing function for Wzx (RfbX): a promising candidate for O-unit flippase.Wzx(RfbX)的O抗原加工功能:O单元翻转酶的一个有潜力的候选者。
J Bacteriol. 1996 Apr;178(7):2102-7. doi: 10.1128/jb.178.7.2102-2107.1996.
6
A novel locus of Yersinia enterocolitica serotype O:3 involved in lipopolysaccharide outer core biosynthesis.小肠结肠炎耶尔森菌O:3血清型中一个参与脂多糖外核心生物合成的新基因座。
Mol Microbiol. 1995 Aug;17(3):575-94. doi: 10.1111/j.1365-2958.1995.mmi_17030575.x.
7
Molecular characterization of hasB from an operon required for hyaluronic acid synthesis in group A streptococci. Demonstration of UDP-glucose dehydrogenase activity.A群链球菌中透明质酸合成所需操纵子hasB的分子特征。UDP-葡萄糖脱氢酶活性的证明。
J Biol Chem. 1993 Apr 5;268(10):7118-24.
8
Molecular analysis of the 3,6-dideoxyhexose pathway genes of Yersinia pseudotuberculosis serogroup IIA.假结核耶尔森氏菌血清群IIA的3,6-二脱氧己糖途径基因的分子分析。
J Bacteriol. 1993 Mar;175(5):1412-22. doi: 10.1128/jb.175.5.1412-1422.1993.
9
Evolution of Salmonella O antigen variation by interspecific gene transfer on a large scale.通过大规模种间基因转移实现沙门氏菌O抗原变异的进化
Trends Genet. 1993 Jan;9(1):17-22. doi: 10.1016/0168-9525(93)90067-R.
10
Inactivation of the Escherichia coli B41 (O101:K99/F41) rfb gene encoding an 80-kDa polypeptide results in the synthesis of an antigenically altered lipopolysaccharide in E. coli K-12.
Gene. 1993 Jan 15;123(1):9-15. doi: 10.1016/0378-1119(93)90532-8.