甲酸还原途径的酶工程和体内测试。

IF 2.6 Q2 BIOCHEMICAL RESEARCH METHODS
Synthetic biology (Oxford, England) Pub Date : 2021-08-06 eCollection Date: 2021-01-01 DOI:10.1093/synbio/ysab020
Jue Wang, Karl Anderson, Ellen Yang, Lian He, Mary E Lidstrom
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引用次数: 5

摘要

甲酸是一种有吸引力的燃料和化学品可持续微生物生产的原料,但其潜力受到缺乏有效的同化途径的限制。甲酸还原为甲醛将允许有效的下游同化,但没有有效的酶知道这种转化。为了建立两步甲酸还原途径,我们筛选了酰基辅酶a合成酶(ACS)和酰化醛脱氢酶(ACDH)在单碳底物上的活性的天然变体,并鉴定了这两种酶的活性和高表达的同源物。然后我们进行了定向进化,将acdh特异性活性提高了2.5倍,ACS裂解物活性提高了5倍。为了测试我们的途径在体内的活性,我们将其表达在甲基化菌中,甲基化菌可以天然吸收甲醛。虽然这些酶在细胞提取物中有活性,但我们无法检测到甲酸盐对生物质的同化,这表明需要进一步改善甲酸盐的形成。我们的工作为进一步开发甲酸盐同化的多用途途径提供了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Enzyme engineering and <i>in vivo</i> testing of a formate reduction pathway.

Enzyme engineering and <i>in vivo</i> testing of a formate reduction pathway.

Enzyme engineering and <i>in vivo</i> testing of a formate reduction pathway.

Enzyme engineering and in vivo testing of a formate reduction pathway.

Formate is an attractive feedstock for sustainable microbial production of fuels and chemicals, but its potential is limited by the lack of efficient assimilation pathways. The reduction of formate to formaldehyde would allow efficient downstream assimilation, but no efficient enzymes are known for this transformation. To develop a 2-step formate reduction pathway, we screened natural variants of acyl-CoA synthetase (ACS) and acylating aldehyde dehydrogenase (ACDH) for activity on one-carbon substrates and identified active and highly expressed homologs of both enzymes. We then performed directed evolution, increasing ACDH-specific activity by 2.5-fold and ACS lysate activity by 5-fold. To test for the in vivo activity of our pathway, we expressed it in a methylotroph which can natively assimilate formaldehyde. Although the enzymes were active in cell extracts, we could not detect formate assimilation into biomass, indicating that further improvement will be required for formatotrophy. Our work provides a foundation for further development of a versatile pathway for formate assimilation.

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