新型木糖转运体支持大肠杆菌同时消耗葡萄糖和木糖。

IF 4.5 Q1 MICROBIOLOGY mLife Pub Date : 2022-06-10 eCollection Date: 2022-06-01 DOI:10.1002/mlf2.12021
Xinna Zhu, Feiyu Fan, Huanna Qiu, Mengyao Shao, Di Li, Yong Yu, Changhao Bi, Xueli Zhang
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引用次数: 0

摘要

葡萄糖和木糖是木质纤维素的两种主要成分。同时消耗葡萄糖和木糖对工程微生物利用木质纤维素生物质生产燃料和化学品至关重要。虽然许多生产限制已经解决,但葡萄糖诱导的木糖转运抑制仍然是一个挑战。本研究设计了一种基于细胞生长的筛选策略,以鉴定不受葡萄糖抑制的木糖转运体。在大肠杆菌中通过基因阻断葡萄糖通路,使葡萄糖只发挥抑制作用,而细胞则需要木糖作为生存的碳源。通过适应性进化、omics分析和逆向代谢工程,发现了一种不受葡萄糖抑制的新的磷酸烯醇丙酮酸:碳水化合物磷酸转移酶系统(PTS)半乳糖醇转运体(GalABC,由EcolC_1640、EcolC_1641和EcolC_1642基因编码)。腺苷酸环化酶的失活导致 EcolC_1642 基因的表达增加,EcolC_1642(N13S)基因的点突变进一步增强了木糖转运。在第二轮基因挖掘过程中,发现了 AraE 和一种新的木糖 ABC 转运体(AraFGH)。转录调节因子 araC 的点突变(L156I)导致 araE 和 araFGH 基因的表达增加,但没有阿拉伯糖诱导,而 araE 的点突变(D223Y)进一步增强了木糖转运。这些新发现的木糖转运体可支持葡萄糖和木糖的同时消耗,具有利用木质纤维素生产化学品的潜在用途。
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New xylose transporters support the simultaneous consumption of glucose and xylose in Escherichia coli.

Glucose and xylose are two major components of lignocellulose. Simultaneous consumption of glucose and xylose is critical for engineered microorganisms to produce fuels and chemicals from lignocellulosic biomass. Although many production limitations have been resolved, glucose-induced inhibition of xylose transport remains a challenge. In this study, a cell growth-based screening strategy was designed to identify xylose transporters uninhibited by glucose. The glucose pathway was genetically blocked in Escherichia coli so that glucose functions only as an inhibitor and cells need xylose as the carbon source for survival. Through adaptive evolution, omics analysis and reverse metabolic engineering, a new phosphoenolpyruvate: carbohydrate phosphotransferase system (PTS) galactitol transporter (GalABC, encoded by EcolC_1640, EcolC_1641, and EcolC_1642 genes) that is not inhibited by glucose was identified. Inactivation of adenylate cyclase led to increased expression of the EcolC_1642 gene, and a point mutation in gene EcolC_1642 (N13S) further enhanced xylose transport. During the second round of gene mining, AraE and a new ABC transporter (AraFGH) of xylose were identified. A point mutation in the transcription regulator araC (L156I) caused increased expression of araE and araFGH genes without arabinose induction, and a point mutation in araE (D223Y) further enhanced xylose transport. These newly identified xylose transporters can support the simultaneous consumption of glucose and xylose and have potential use in producing chemicals from lignocellulose.

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