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利用异源芳香羧酸还原酶由谷氨酸棒杆菌生产香草醛。

Vanillin production by Corynebacterium glutamicum using heterologous aromatic carboxylic acid reductases.

作者信息

Matsuzawa Miku, Ito Junko, Danjo Keiko, Fukui Keita

机构信息

Research Institute for Bioscience Products & Fine Chemicals, Ajinomoto Co., Inc, Kawasaki, Kanagawa, 210-8681, Japan.

出版信息

Biotechnol Biofuels Bioprod. 2024 May 1;17(1):58. doi: 10.1186/s13068-024-02507-3.

Abstract

BACKGROUND

Vanillin is a flavoring substance derived from vanilla. We are currently developing a biotransformation method for vanillin production using glucose. This report describes the last step in vanillin production: the conversion of vanillic acid to vanillin. First, we selected Corynebacterium glutamicum as the host owing to its high vanillin resistance. The aromatic aldehyde reductase gene (NCgl0324) and vanillic acid demethylase protein subunits A and B gene (vanAB, NCgl2300-NCgl2301) were deleted in C. glutamicum genome to avoid vanillin degradation. Next, we searched for an aromatic carboxylic acid reductase (ACAR), which converts vanillic acid to vanillin. Seventeen ACAR homologs from various organisms were introduced into C. glutamicum.

RESULTS

In vivo conversion experiments showed that eight ACARs were successfully expressed and produced vanillin. In terms of conversion activity and substrate specificity, the ACARs from Gordonia effusa, Coccomyxa subellipsoidea, and Novosphingobium malaysiense are promising candidates for commercial production.

CONCLUSIONS

Corynebacterium glutamicum harboring Gordonia effusa ACAR produced 22 g/L vanillin, which is, to the best of our knowledge, the highest accumulation reported in the literature. At the same time, we discovered ACAR from Novosphingobium malaysiense and Coccomyxa subellipsoidea C-169 with high substrate specificity. These findings are useful for reducing the byproducts.

摘要

背景

香草醛是一种从香草中提取的调味物质。我们目前正在开发一种利用葡萄糖生产香草醛的生物转化方法。本报告描述了香草醛生产的最后一步:香草酸转化为香草醛。首先,由于谷氨酸棒杆菌对香草醛具有高抗性,我们选择其作为宿主。在谷氨酸棒杆菌基因组中删除了芳香醛还原酶基因(NCgl0324)以及香草酸脱甲基酶蛋白亚基A和B的基因(vanAB,NCgl2300 - NCgl2301),以避免香草醛降解。接下来,我们寻找一种将香草酸转化为香草醛的芳香羧酸还原酶(ACAR)。将来自各种生物体的17种ACAR同源物导入谷氨酸棒杆菌。

结果

体内转化实验表明,8种ACAR成功表达并产生了香草醛。就转化活性和底物特异性而言,来自戈登氏菌、椭圆小球藻和马来西亚新鞘氨醇菌的ACAR是商业生产的有前景的候选者。

结论

携带戈登氏菌ACAR的谷氨酸棒杆菌产生了22 g/L香草醛,据我们所知,这是文献中报道的最高积累量。同时,我们发现了来自马来西亚新鞘氨醇菌和椭圆小球藻C - 169的具有高底物特异性的ACAR。这些发现有助于减少副产物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2006/11064420/aaadb67349ff/13068_2024_2507_Fig1_HTML.jpg

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