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用于咖啡因和可可碱生产的酿酒酵母的代谢工程。

Metabolic engineering of Saccharomyces cerevisiae for caffeine and theobromine production.

作者信息

Jin Lu, Bhuiya Mohammad Wadud, Li Mengmeng, Liu XiangQi, Han Jixiang, Deng WeiWei, Wang Min, Yu Oliver, Zhang Zhengzhu

机构信息

Key Laboratory of Tea Biochemistry and Biotechnology, Ministry of Education, Anhui Agricultural University, Hefei, PR China.

Conagen Inc., St. Louis, Missouri, United States of America.

出版信息

PLoS One. 2014 Aug 18;9(8):e105368. doi: 10.1371/journal.pone.0105368. eCollection 2014.

Abstract

Caffeine (1, 3, 7-trimethylxanthine) and theobromine (3, 7-dimethylxanthine) are the major purine alkaloids in plants, e.g., tea (Camellia sinensis) and coffee (Coffea arabica). Caffeine is a major component of coffee and is used widely in food and beverage industries. Most of the enzymes involved in the caffeine biosynthetic pathway have been reported previously. Here, we demonstrated the biosynthesis of caffeine (0.38 mg/L) by co-expression of Coffea arabica xanthosine methyltransferase (CaXMT) and Camellia sinensis caffeine synthase (TCS) in Saccharomyces cerevisiae. Furthermore, we endeavored to develop this production platform for making other purine-based alkaloids. To increase the catalytic activity of TCS in an effort to increase theobromine production, we identified four amino acid residues based on structural analyses of 3D-model of TCS. Two TCS1 mutants (Val317Met and Phe217Trp) slightly increased in theobromine accumulation and simultaneously decreased in caffeine production. The application and further optimization of this biosynthetic platform are discussed.

摘要

咖啡因(1,3,7-三甲基黄嘌呤)和可可碱(3,7-二甲基黄嘌呤)是植物中的主要嘌呤生物碱,例如茶叶(茶树)和咖啡(阿拉伯咖啡)。咖啡因是咖啡的主要成分,在食品和饮料行业中广泛使用。先前已报道了咖啡因生物合成途径中涉及的大多数酶。在此,我们通过在酿酒酵母中共表达阿拉伯咖啡黄嘌呤甲基转移酶(CaXMT)和茶树咖啡因合酶(TCS),证明了咖啡因(0.38毫克/升)的生物合成。此外,我们致力于开发这个生产平台以制造其他基于嘌呤的生物碱。为了提高TCS的催化活性以增加可可碱的产量,我们基于TCS的3D模型的结构分析鉴定了四个氨基酸残基。两个TCS1突变体(Val317Met和Phe217Trp)可可碱积累略有增加,同时咖啡因产量下降。本文讨论了该生物合成平台的应用和进一步优化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f89/4136831/0b09c70a23f8/pone.0105368.g001.jpg

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