Metabolic engineering for microbial production of sugar acids.

IF 3.5 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Fatma Gizem Avci, Tim Prasun, Volker F Wendisch
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引用次数: 0

Abstract

Carbohydrates including sugar acids are commonly used as carbon sources in microbial biotechnology. These sugar acids are themselves desirable and often overlooked targets for biobased production since they find applications in a broad range of industries, examples include food, construction, medical, textile, and polymer industries. Different stages of oxidation for natural sugar acids can be distinguished. Oxidation of the aldehyde group yields aldonic acids, oxidation of the primary hydroxy group leads to uronic acids, and both oxidations combined yield aldaric acids. While the chemical oxidation of sugars to their acid forms often is a one-pot reaction under harsh conditions, their biosynthesis is much more delicate. Bio-based production can involve enzymatic conversion, whole-cell biotransformation, and fermentation. Generally, the in vivo approaches are preferred because they are less resource-intensive than enzymatic conversion. Metabolic engineering plays a crucial role in optimizing microbial strains for efficient sugar acid production. Strategies include pathway engineering to overexpress key enzymes involved in sugar oxidation, deletion of competing pathways to enhance the precursor availability and eliminate the product consumption, cofactor balancing for efficient redox reactions, and transporter engineering to facilitate precursor import or sugar acid export. Synthetic biology tools, such as CRISPR-Cas and dynamic regulatory circuits, have further improved strain development by enabling precise genetic modifications and adaptive control of metabolic fluxes. The usage of plant biomass hydrolysates for bio-based production further adds to the environmental friendliness of the in vivo approaches. This review highlights the different approaches for the production of C5 and C6 sugar acids, their applications, and their catabolism in microbes.

微生物生产糖酸的代谢工程。
包括糖酸在内的碳水化合物是微生物生物技术中常用的碳源。这些糖酸本身是理想的,但往往被忽视的生物基生产目标,因为它们在广泛的行业中得到应用,例如食品,建筑,医疗,纺织和聚合物行业。天然糖酸氧化的不同阶段是可以区分的。醛基氧化生成醛酸,伯羟基氧化生成醛酸,两种氧化结合生成醛酸。虽然在恶劣的条件下,糖的化学氧化通常是一锅反应,但它们的生物合成要微妙得多。生物基生产包括酶转化、全细胞生物转化和发酵。一般来说,体内方法是首选的,因为它们比酶转化的资源密集程度低。代谢工程在优化微生物菌株以高效产糖酸方面起着至关重要的作用。策略包括通路工程以过度表达参与糖氧化的关键酶,删除竞争通路以提高前体可用性并消除产品消耗,平衡辅助因子以实现有效的氧化还原反应,以及转运体工程以促进前体进口或糖酸出口。合成生物学工具,如CRISPR-Cas和动态调控电路,通过实现精确的遗传修饰和对代谢通量的适应性控制,进一步改善了菌株的发育。利用植物生物质水解物进行生物基生产进一步增加了体内方法的环境友好性。本文综述了C5和C6糖酸的不同生产方法、应用及其在微生物中的分解代谢。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Biotechnology
BMC Biotechnology 工程技术-生物工程与应用微生物
CiteScore
6.60
自引率
0.00%
发文量
34
审稿时长
2 months
期刊介绍: BMC Biotechnology is an open access, peer-reviewed journal that considers articles on the manipulation of biological macromolecules or organisms for use in experimental procedures, cellular and tissue engineering or in the pharmaceutical, agricultural biotechnology and allied industries.
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