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利用高浓度乙酸开发积累琥珀酸的超耐受菌株。

Development of Hypertolerant Strain of Accumulating Succinic Acid Using High Levels of Acetate.

作者信息

Narisetty Vivek, Prabhu Ashish A, Bommareddy Rajesh Reddy, Cox Rylan, Agrawal Deepti, Misra Ashish, Haider M Ali, Bhatnagar Amit, Pandey Ashok, Kumar Vinod

机构信息

School of Water, Energy and Environment, Cranfield University, Cranfield MK43 0AL, United Kingdom.

Department of Applied Sciences, Northumbria University, Newcastle Upon Tyne NE1 8ST, United Kingdom.

出版信息

ACS Sustain Chem Eng. 2022 Aug 22;10(33):10858-10869. doi: 10.1021/acssuschemeng.2c02408. Epub 2022 Aug 9.

Abstract

Acetate is emerging as a promising feedstock for biorefineries as it can serve as an alternate carbon source for microbial cell factories. In this study, we expressed acetyl-CoA synthase in PSA02004PP, and the recombinant strain grew on acetate as the sole carbon source and accumulated succinic acid or succinate (SA). Unlike traditional feedstocks, acetate is a toxic substrate for microorganisms; therefore, the recombinant strain was further subjected to adaptive laboratory evolution to alleviate toxicity and improve tolerance against acetate. At high acetate concentrations, the adapted strain ACS 5.0 grew rapidly and accumulated lipids and SA. Bioreactor cultivation of ACS 5.0 with 22.5 g/L acetate in a batch mode resulted in a maximum cell OD of 9.2, with lipid and SA accumulation being 0.84 and 5.1 g/L, respectively. However, its fed-batch cultivation yielded a cell OD of 23.5, SA titer of 6.5 g/L, and lipid production of 1.5 g/L with an acetate uptake rate of 0.2 g/L h, about 2.86 times higher than the parent strain. Cofermentation of acetate and glucose significantly enhanced the SA titer and lipid accumulation to 12.2 and 1.8 g/L, respectively, with marginal increment in cell growth (OD: 26.7). Furthermore, metabolic flux analysis has drawn insights into utilizing acetate for the production of metabolites that are downstream to acetyl-CoA. To the best of our knowledge, this is the first report on SA production from acetate by and demonstrates a path for direct valorization of sugar-rich biomass hydrolysates with elevated acetate levels to SA.

摘要

乙酸盐正成为生物精炼厂一种有前景的原料,因为它可作为微生物细胞工厂的替代碳源。在本研究中,我们在PSA02004PP中表达了乙酰辅酶A合成酶,该重组菌株能以乙酸盐作为唯一碳源生长,并积累琥珀酸或琥珀酸盐(SA)。与传统原料不同,乙酸盐对微生物是一种有毒底物;因此,对该重组菌株进一步进行适应性实验室进化,以减轻毒性并提高对乙酸盐的耐受性。在高乙酸盐浓度下,适应性菌株ACS 5.0生长迅速,并积累脂质和SA。以分批模式用22.5 g/L乙酸盐对ACS 5.0进行生物反应器培养,最大细胞光密度(OD)为9.2,脂质和SA积累量分别为0.84 g/L和5.1 g/L。然而,其补料分批培养得到的细胞OD为23.5,SA产量为6.5 g/L,脂质产量为1.5 g/L,乙酸盐摄取速率为0.2 g/(L·h),约为亲本菌株的2.86倍。乙酸盐和葡萄糖的共发酵显著提高了SA产量和脂质积累量,分别达到12.2 g/L和1.8 g/L,细胞生长仅有少量增加(OD:26.7)。此外,代谢通量分析为利用乙酸盐生产乙酰辅酶A下游代谢物提供了见解。据我们所知,这是关于利用乙酸盐生产SA的首次报道,并展示了一条将富含糖的生物质水解物中乙酸盐含量升高直接转化为SA的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1068/9400109/f8f0fdf17041/sc2c02408_0002.jpg

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