首页> 美国卫生研究院文献>Metabolic Engineering Communications >Alone at last! – Heterologous expression of a single gene is sufficient for establishing the five-step Weimberg pathway in Corynebacterium glutamicum
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Alone at last! – Heterologous expression of a single gene is sufficient for establishing the five-step Weimberg pathway in Corynebacterium glutamicum

机译:孤独终老! –单个基因的异源表达足以在谷氨酸棒杆菌中建立五步Weimberg途径

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摘要

Corynebacterium glutamicum can grow on d-xylose as sole carbon and energy source via the five-step Weimberg pathway when the pentacistronic xylXABCD operon from Caulobacter crescentus is heterologously expressed. More recently, it could be demonstrated that the C. glutamicum wild type accumulates the Weimberg pathway intermediate d-xylonate when cultivated in the presence of d-xylose. Reason for this is the activity of the endogenous dehydrogenase IolG, which can also oxidize d-xylose. This raised the question whether additional endogenous enzymes in C. glutamicum contribute to the catabolization of d-xylose via the Weimberg pathway. In this study, analysis of the C. glutamicum genome in combination with systematic reduction of the heterologous xylXABCD operon revealed that the hitherto unknown and endogenous dehydrogenase KsaD (Cg0535) can also oxidize α-ketoglutarate semialdehyde to the tricarboxylic acid cycle intermediate α-ketoglutarate, the final enzymatic step of the Weimberg pathway. Furthermore, heterologous expression of either xylX or xylD, encoding for the two dehydratases of the Weimberg pathway in C. crescentus, is sufficient for enabling C. glutamicum to grow on d-xylose as sole carbon and energy source. Finally, several variants for the carbon-efficient microbial production of α-ketoglutarate from d-xylose were constructed. In comparison to cultivation solely on d-glucose, the best strain accumulated up to 1.5-fold more α-ketoglutarate in d-xylose/d-glucose mixtures.
机译:当来自新月形杆菌的五顺反子xylXABCD操纵子异源表达时,谷氨酸棒杆菌可以通过五步Weimberg途径在d-木糖上作为唯一碳和能源生长。最近,有证据表明,当在D-木糖存在下培养时,谷氨酸棒杆菌野生型在D-木糖酸盐的Weimberg途径中间积累。造成这种情况的原因是内源性脱氢酶IolG的活性,它也可以氧化D-木糖。这就提出了一个问题,即谷氨酸棒杆菌中的其他内源酶是否通过Weimberg途径促进了D-木糖的分解。在这项研究中,对谷氨酸棒杆菌基因组的分析与异源xylXABCD操纵子的系统还原相结合,揭示了迄今为止未知的内源性脱氢酶KsaD(Cg0535)还可将α-酮戊二酸半醛氧化为三羧酸循环中间体α-酮戊二酸,温伯格途径的最后一个酶促步骤。此外,编码C.crescentus中Weimberg途径的两个脱水酶的xylX或xylD的异源表达足以使谷氨酸棒杆菌能够在d-木糖上生长作为唯一碳和能源。最后,构建了几种从d-木糖生产碳高效微生物生产α-酮戊二酸的变体。与仅在d-葡萄糖上进行培养相比,最佳菌株在d-木糖/ d-葡萄糖混合物中累积的α-酮戊二酸多1.5倍。

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