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系统代谢工程提高热带假丝酵母中芳樟醇的合成。

Systematic metabolic engineering for improved synthesis of perillic acid in Candida tropicalis.

机构信息

The Key Laboratory of Carbohydrate Chemistry and Biotechnology, Ministry of Education, School of Biotechnology, Jiangnan University, Wuxi, 214122, China.

The Key Laboratory of Industrial Biotechnology, Ministry of Education, School of Biotechnology, Jiangnan University, Wuxi, 214122, China.

出版信息

Appl Microbiol Biotechnol. 2024 Aug 27;108(1):447. doi: 10.1007/s00253-024-13279-z.

Abstract

Perillic acid has been studied as an anticancer and antimicrobial drug. Production of perillic acid has attracted considerable attention. Meanwhile, Candida tropicalis is an unconventional diploid yeast, most significantly characterized by its ability to metabolize alkanes or fatty acids for growth and proliferation. Therefore, perillic acid's precursor (L-limonene) in C. tropicalis was firstly synthesized by expressing a Mentha spicata L-limonene synthase gene, LS_Ms in this work. Expression of a gene which encoded for a truncated version of tLS_Ms increased the production of L-limonene with a 2.78-fold increase in the titer over C. tropicalis GJR-LS-01. Compartmentalized expression of the gene tLS_Ms inhibited the production of L-limonene in C. tropicalis compared to cytoplasmic expression. Cytoplasmic overexpression of seven precursor synthesis genes significantly enhanced the production of L-limonene in C. tropicalis compared to their compartmentalized expression (mitochondria or peroxisomes), which increased by 31.7-fold in C. tropicalis GJR-tLS-01. The L-limonene titer in C. tropicalis GJR-EW-tLS-04 overexpressing the mutant gene ERG20WW in the cytoplasm was significantly increased, 11.33-fold higher than the control. The titer of L-limonene for 60 g/L glucose was increased by 1.40-fold compared to the control. Finally, a Salvia miltiorrhiza cytochrome P450 enzyme gene CYP7176 and an Arabidopsis thaliana NADPH cytochrome P450 reductase gene CPR were heterologously expressed in C. tropicalis GJR-EW-tLS-04C for the synthesis of perillic acid, which reached a titer of 106.69 mg/L in a 5-L fermenter. This is the first report of de novo synthesis of perillic acid in engineered microorganisms. The results also showed that other chemicals may be efficiently produced in C. tropicalis. KEY POINTS: • Key genes cytoplasmic expression was conducive to L-limonene production in C. tropicalis. • Perillic acid was first synthesized de novo in engineered microorganisms. • The titer of perillic acid reached 106.69 mg/L in a 5-L fermenter.

摘要

壬酸已被研究为一种抗癌和抗菌药物。壬酸的生产引起了相当大的关注。同时,热带假丝酵母是一种非常规的二倍体酵母,最显著的特点是能够代谢烷烃或脂肪酸进行生长和增殖。因此,在这项工作中,首先通过在热带假丝酵母中表达薄荷属 L-柠檬烯合酶基因 LS_Ms 来合成壬酸的前体(L-柠檬烯)。与细胞质表达相比,表达编码 tLS_Ms 的截断版本的基因增加了 L-柠檬烯的产量,比 GJR-LS-01 中的产量增加了 2.78 倍。基因 tLS_Ms 的区室化表达抑制了 L-柠檬烯在热带假丝酵母中的产生。与区室化表达(线粒体或过氧化物酶体)相比,细胞质过表达七种前体合成基因显著提高了 L-柠檬烯在热带假丝酵母中的产量,在 GJR-tLS-01 中增加了 31.7 倍。在细胞质中过表达突变基因 ERG20WW 的热带假丝酵母 GJR-EW-tLS-04 中,L-柠檬烯的产量明显增加,比对照高 11.33 倍。与对照相比,60 g/L 葡萄糖的 L-柠檬烯产量增加了 1.40 倍。最后,在热带假丝酵母 GJR-EW-tLS-04C 中异源表达丹参细胞色素 P450 酶基因 CYP7176 和拟南芥 NADPH 细胞色素 P450 还原酶基因 CPR,用于合成壬酸,在 5-L 发酵罐中达到 106.69 mg/L 的产量。这是首次在工程微生物中从头合成壬酸。结果还表明,其他化学物质也可能在热带假丝酵母中有效生产。要点:• 关键基因的细胞质表达有利于热带假丝酵母中 L-柠檬烯的生产。• 壬酸首次在工程微生物中从头合成。• 在 5-L 发酵罐中,壬酸的产量达到 106.69 mg/L。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/769f/11349783/7a0c2e012844/253_2024_13279_Fig1_HTML.jpg

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