首页> 美国卫生研究院文献>Journal of Bacteriology >Activity of CMP-2-keto-3-deoxyoctulosonic acid synthetase in Escherichia coli strains expressing the capsular K5 polysaccharide implication for K5 polysaccharide biosynthesis.
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Activity of CMP-2-keto-3-deoxyoctulosonic acid synthetase in Escherichia coli strains expressing the capsular K5 polysaccharide implication for K5 polysaccharide biosynthesis.

机译:CMP-2-酮-3-脱氧辛酸合成酶在表达荚膜K5多糖的大肠杆菌菌株中的活性对K5多糖的生物合成有影响。

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摘要

The activity of the cytoplasmic CMP-2-keto-3-deoxyoctulosonic acid synthetase (CMP-KDO synthetase), which is low in Escherichia coli rough strains such as E. coli K-12 and in uncapsulated strains such as E. coli O111, was significantly elevated in encapsulated E. coli O10:K5 and O18:K5. This enzyme activity was even higher in an E. coli clone expressing the K5 capsule. This and the following findings suggest a correlation between elevated CMP-KDO synthetase activity and the biosynthesis of the capsular K5 polysaccharide. (i) Expression of the K5 polysaccharide and elevated CMP-KDO synthetase activity were observed with bacteria grown at 37 degrees C but not with cells grown at 20 degrees C or below. (ii) The recovery kinetics of capsule expression of intact bacteria, in vitro K5 polysaccharide-synthesizing activity of bacteria, and CMP-KDO synthetase activity of bacteria after temperature upshift from 18 to 37 degrees C were the same. (iii) Chemicals which inhibit capsule (polysaccharide) expression also inhibited the elevation of CMP-KDO synthetase activity. The chromosomal location of the gene responsible for the elevation of this enzyme activity was narrowed down to the distal segment of the transport region of the K5 expression genes.
机译:胞质CMP-2-酮-3-脱氧辛酸合成酶(CMP-KDO合成酶)的活性在大肠杆菌粗糙菌株(如大肠杆菌K-12)和未包囊菌株(如大肠杆菌O111)中较低,在包封的大肠杆菌O10:K5和O18:K5中,其显着升高。在表达K5胶囊的大肠杆菌克隆中,该酶活性甚至更高。该发现和以下发现表明,CMP-KDO合成酶活性升高与荚膜K5多糖的生物合成之间存在相关性。 (i)在37℃下生长的细菌观察到K5多糖的表达和提高的CMP-KDO合成酶活性,而在20℃或以下生长的细胞观察不到。 (ii)温度从18升至37摄氏度后,完整细菌的胶囊表达恢复动力学,细菌的体外K5多糖合成活性以及细菌CMP-KDO合成酶活性相同。 (iii)抑制胶囊(多糖)表达的化学物质也抑制了CMP-KDO合成酶活性的升高。负责提高这种酶活性的基因的染色体位置被缩小到K5表达基因的转运区域的远端。

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