Inactivation of mdoH leads to increased expression of colanic acid capsular polysaccharide in Escherichia coli

Inactivation of mdoH leads to increased expression of colanic acid capsular polysaccharide in Escherichia coli
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DOI:
10.1128/jb.179.21.6858-6861.1997
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发表时间:
1997-11-01
影响因子:
3.2
通讯作者:
Trempy, JE
Trempy, JE
中科院分区:
生物学3区
文献类型:
--
作者:
Ebel, W;Vaughn, GJ;Trempy, JE

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在大肠杆菌lon(+)细胞中通常以低水平表达的荚膜基因(cps)表达,在携带Tn10::Delta kan插入的lon(+)细胞中增加了38倍,在E. coli染色体。rcsA、rcsB或rcsC中的突变消除了Tn10::Delta kan插入的效应。对Tn10::Delta kan插入的两侧进行测序,将插入定位于先前报道的mdoH基因,该基因编码一种参与膜衍生寡糖(MDO)生物合成的蛋白质。提出了一个模型,表明MDO的周质水平的行为,以信号RcsC激活cps的表达。
Capsule gene (cps) expression, which normally occurs at low levels in Escherichia coli lon(+) cells, increased 38-fold in lon(+) cells carrying a Tn10::Delta kan insertion mapping to 24 min on the E. coli chromosome. Null mutations in rcsA, rcsB, or rcsC abolished the effect of the Tn10::Delta kan insertion. Sequencing of both sides of the Tn10::Delta kan insertion localized the insertion to the previously reported mdoH gene, which encodes a protein involved in biosynthesis of membrane-derived oligosaccharides (MDOs). A model suggesting that the periplasmic levels of MDOs act to signal RcsC to activate cps expression is proposed.