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Solute Transport Proteins and the Outer Membrane Protein NmpC Contribute to Heat Resistance of Escherichia coli AW1.7

机译:溶质运输蛋白和外膜蛋白NmpC有助于大肠杆菌AW1.7的耐热性

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This study aimed to elucidate determinants of heat resistance in Escherichia coli by comparing the composition of membrane lipids, as well as gene expression, in heat-resistant E. coli AW1.7 and heat-sensitive E. coli GGG10 with or without heat shock. The survival of E. coli AW1.7 at late exponential phase was 100-fold higher than that of E. coli GGG10 after incubation at 60°C for 15 min. The cytoplasmic membrane of E. coli AW1.7 contained a higher proportion of saturated and cyclopropane fatty acids than that of E. coli GGG10. Microarray hybridization of cDNA libraries obtained from exponentially growing or heat-shocked cultures was performed to compare gene expression in these two strains. Expression of selected genes from different functional groups was quantified by quantitative PCR. DnaK and 30S and 50S ribosomal subunits were overexpressed in E. coli GGG10 relative to E. coli AW1.7 upon heat shock at 50°C, indicating improved ribosome stability. The outer membrane porin NmpC and several transport proteins were overexpressed in exponentially growing E. coli AW1.7. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis of membrane properties confirmed that NmpC is present in the outer membrane of E. coli AW1.7 but not in that of E. coli GGG10. Expression of NmpC in E. coli GGG10 increased survival at 60°C 50- to 1,000-fold. In conclusion, the outer membrane porin NmpC contributes to heat resistance in E. coli AW1.7, but the heat resistance of this strain is dependent on additional factors, which likely include the composition of membrane lipids, as well as solute transport proteins.
机译:这项研究旨在通过比较耐热或不耐热的大肠杆菌AW1.7和热敏大肠杆菌GGG10中膜脂的组成以及基因表达,阐明大肠杆菌的耐热性决定因素。在60°C孵育15分钟后,大肠杆菌AW1.7在指数后期的存活率比大肠杆菌GGG10高100倍。大肠杆菌AW1.7的细胞质膜所含的饱和脂肪酸和环丙烷脂肪酸的含量比大肠杆菌GGG10高。进行了从指数生长或热激培养物中获得的cDNA文库的微阵列杂交,以比较这两个菌株中的基因表达。通过定量PCR对来自不同功能组的所选基因的表达进行定量。在50°C的热冲击下,相对于大肠杆菌AW1.7,DnaK和30S和50S核糖体亚基在大肠杆菌GGG10中过表达,表明核糖体稳定性提高。外膜孔蛋白NmpC和几种转运蛋白在指数增长的大肠杆菌AW1.7中过表达。膜特性的十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分析证实,NmpC存在于大肠杆菌AW1.7的外膜中,而不存在于大肠杆菌GGG10的外膜中。 NmpC在大肠杆菌GGG10中的表达将其在60°C的存活率提高了50到1,000倍。总之,外膜孔蛋白NmpC有助于大肠杆菌AW1.7的耐热性,但是该菌株的耐热性取决于其他因素,这些因素可能包括膜脂质的组成以及溶质转运蛋白。

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