Production of propionic acid through biotransformation of glucose and d-lactic acid by construction of synthetic acrylate pathway in metabolically engineered E. coli

IF 1.4 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Anitha Janet Roshni Yesudhas, Padmapriya Ganapathy Raman, Akila Thirumalai, Shuchi Saxena, R. Subramanian
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引用次数: 1

Abstract

Abstract Construction of an efficient synthetic acrylate pathway in recombinant hosts such as E. coli and lactic acid bacteria should lead to synthesis of an array of products such as propionic acid, β-alanine, α-amino butyric acid and other products. The major bottlenecks impeding the titre of propionic acid, from d-lactate via the acrylate pathway in Escherichia coli and Lactococcus lactis, mainly include regulatory hurdles, inefficiency of enzymes involved in production and inability to overexpress multiple enzymes in soluble functional form along with other factors. In this work, the three enzymes, propionyl-CoA transferase (Pct) and acryloyl-CoA reductase (Acr) from E. coli, and lactoyl-CoA dehydratase (Lcd) from Megasphaera elsdenii, that possess better kinetic parameters and reduced size, have been recruited based on the insights gained from kinetic modelling of the acrylate pathway. Secondly, a common strategy for functional expression of these pathway enzymes has been demonstrated to improve their specific activities. The expression levels of Pct, Acr and Lcd were enhanced by sorbitol-induced native folding, with exposure to heat and low expression temperature, resulting in 11-, 4- and 4-fold higher yield of soluble protein than in the control. The specific activities of Pct and Acr were 39- and 34-fold higher than Clostridium propionicum counterparts. Also, the enzyme activity of Lcd was equivalent to that in the native producer, C. propionicum. The recombinant strains exhibited 11% and 20% lesser growth rates than in the control with propionate titre of 240 mg/L and 320 mg/L when grown in glucose and d-lactate, respectively. The yields of propionic acid from glucose and lactic acid were 5% and 32%, respectively. Further improvement in yields should be achieved by expressing all the enzymes in sufficient amount and appropriate ratios, overcoming all the regulatory hurdles.
在代谢工程大肠杆菌中构建合成丙烯酸酯途径生物转化葡萄糖和d-乳酸生产丙酸
摘要在大肠杆菌和乳酸菌等重组宿主中构建高效的合成丙烯酸酯途径,可以合成丙酸、β-丙氨酸、α-氨基丁酸等一系列产物。阻碍丙酸在大肠杆菌和乳酸乳球菌中通过丙烯酸酯途径从d-乳酸中滴定的主要瓶颈主要包括调节障碍、参与生产的酶效率低下、无法过表达可溶性功能形式的多种酶以及其他因素。在这项工作中,基于从丙烯酸酯途径的动力学建模中获得的见解,招募了三种酶,即来自大肠杆菌的丙酰基辅酶A转移酶(Pct)和丙烯酰基辅酶A还原酶(Acr),以及来自大球藻的乳糖基辅酶A脱水酶(Lcd),它们具有更好的动力学参数和更小的尺寸。其次,这些途径酶的功能表达的常见策略已被证明可以提高其特异性活性。在高温和低表达温度下,山梨醇诱导的天然折叠增强了Pct、Acr和Lcd的表达水平,导致可溶性蛋白的产量比对照高11倍、4倍和4倍。Pct和Acr的比活性分别是丙酸梭菌的39倍和34倍。此外,Lcd的酶活性与天然生产者丙酸梭菌的酶活性相当。重组菌株表现出比对照低11%和20%的生长率,丙酸盐滴度为240 mg/L和320 当分别在葡萄糖和d-乳酸中生长时。由葡萄糖和乳酸制备丙酸的产率分别为5%和32%。产量的进一步提高应该通过以足够的量和适当的比例表达所有的酶来实现,克服所有的调节障碍。
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来源期刊
Biocatalysis and Biotransformation
Biocatalysis and Biotransformation 生物-生化与分子生物学
CiteScore
4.40
自引率
5.60%
发文量
37
审稿时长
3 months
期刊介绍: Biocatalysis and Biotransformation publishes high quality research on the application of biological catalysts for the synthesis, interconversion or degradation of chemical species. Papers are published in the areas of: Mechanistic principles Kinetics and thermodynamics of biocatalytic processes Chemical or genetic modification of biocatalysts Developments in biocatalyst''s immobilization Activity and stability of biocatalysts in non-aqueous and multi-phasic environments, including the design of large scale biocatalytic processes Biomimetic systems Environmental applications of biocatalysis Metabolic engineering Types of articles published are; full-length original research articles, reviews, short communications on the application of biotransformations, and preliminary reports of novel catalytic activities.
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