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Transcriptomic analysis of an l-threonine-producing Escherichia coli TWF001

机译:产高苏氨酸大肠杆菌TWF001的转录组分析

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Wild-type Escherichia coli usually does not accumulate l-threonine, but E. coli strain TWF001 could produce 30.35 g/L l-threonine after 23-H fed-batch fermentation. To understand the mechanism for the high yield of l-threonine production in TWF001, transcriptomic analyses of the TWF001 cell samples collected at the logarithmic and stationary phases were performed, using the wild-type E. coli strain W3110 as the control. Compared with W3110, 1739 and 2361 genes were differentially transcribed in the logarithmic and stationary phases, respectively. Most genes related to the biosynthesis of l-threonine were significantly upregulated. Some key genes related to the NAD(P)H regeneration were upregulated. Many genes relevant to glycolysis and TCA cycle were downregulated. The key genes involved in the l-threonine degradation were downregulated. The gene rhtA encoding the l-threonine exporter was upregulated, whereas the genes sstT and tdcC encoding the l-threonine importer were downregulated. The upregulated genes in the glutamate pathway might form an amino-providing loop, which is beneficial for the high yield of l-threonine production. Many genes encoding the 30S and 50S subunits of ribosomes were also upregulated. The findings are useful for gene engineering to increase l-threonine production in E. coli.
机译:野生型大肠杆菌通常不会累积L-苏氨酸,但大肠杆菌菌株TWF001可在23小时喂食批量发酵后产生30.35克/升L-Threonine。为了了解TWF001中L-苏氨酸产生的高产量的机制,使用野生型大肠杆菌菌株W3110作为对照进行在对数和固定相时收集的TWF001细胞样品的转录组分析。与W3110,1739和2361个基因分别在对数和固定阶段进行差异转录。大多数与L-苏氨酸生物合成相关的基因显着上调。上调了与NAD(P)H再生相关的一些关键基因。下调许多与糖酵解和TCA循环相关的基因。涉及L-苏氨酸降解的关键基因被下调。编码L-苏氨酸出口国的基因rhTA被上调,而编码L-苏氨酸进口剂的基因和TDCC被下调。谷氨酸途径中的上调基因可以形成氨基提供环,这对于L-苏氨酸产生的高产量有益。还上调了编码30S和50S亚基的许多基因也被上调。该发现对于基因工程有助于增加大肠杆菌的L-苏氨酸产生。

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