研究报告

基于地衣芽孢杆菌表达系统搭建左旋多巴新合成体系

  • 李乐云 ,
  • 李由然 ,
  • 许银彪 ,
  • 张梁 ,
  • 顾正华 ,
  • 丁重阳 ,
  • 石贵阳
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  • 1(粮食发酵工艺与技术国家工程实验室(江南大学),江苏 无锡,214122)
    2(江南大学 生物工程学院,江苏 无锡,214122)
硕士研究生(石贵阳教授为通讯作者,E-mail:gyshi@jiangnan.edu.cn)

收稿日期: 2020-02-06

  网络出版日期: 2020-06-24

基金资助

轻工业技术与工程国家一流学科计划(LITE2018-22)

Preparation of L-DOPA from tyrosine by biotransformation usingBacillus licheniformis strains expressed tyrosine 3-monooxygenase andsepiapterin reductase

  • LI Leyun ,
  • LI Youran ,
  • XU Yinbiao ,
  • ZHANG Liang ,
  • GU Zhenghua ,
  • DING Zhongyang ,
  • SHI Guiyang
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  • 1(National Engineering Laboratory for Cereal Fermentation Technology, Jiangnan University, Wuxi 214122, China)
    2(School of Biotechnology, Jiangnan University, Wuxi 214122, China)

Received date: 2020-02-06

  Online published: 2020-06-24

摘要

左旋多巴(3,4-dihydroxylphenylalanine, L-DOPA)是一种L-酪氨酸(L-tyrosine, L-Tyr)的氨基酸类似物,在临床医学、美容保健等领域具有广阔的应用前景。通过生物信息学方法挖掘到Streptosporangium roseum DSM 43021来源的酪氨酸羟化酶(tyrosine hydroxylase, TH)基因(srth)在地衣芽孢杆菌(Bacillus licheniformis)中重组表达,结合墨蝶呤还原酶重组菌以L-Tyr为底物进行全细胞联合转化合成L-DOPA,并初步探究其催化过程。结果显示,srth具有保守的Fe2+及底物喋呤的氨基酸结合位点,与人来源的TH亲缘关系较远。SrTH蛋白胞内粗酶活力为30.7 U/mL,胞外酶活力为22.79 U/mL。利用srth重组菌Bl/pMH与墨蝶呤还原酶重组菌Bl/pMF全细胞联合转化L-Tyr,成功合成L-DOPA。TH催化合成L-DOPA过程中,四氢生物蝶呤(tetrahydrobiopterin, BH4)是限制酶反应进行的重要因素,L-Tyr的消耗量与BH4的需求量之比约为1∶2。研究首次实现了TH在地衣芽孢菌中的表达,成功基于B. licheniformis表达系统搭建L-DOPA新合成体系,对拓展酶催化法高效合成L-DOPA具有重要的指导意义和应用潜力。

本文引用格式

李乐云 , 李由然 , 许银彪 , 张梁 , 顾正华 , 丁重阳 , 石贵阳 . 基于地衣芽孢杆菌表达系统搭建左旋多巴新合成体系[J]. 食品与发酵工业, 2020 , 46(11) : 23 -31 . DOI: 10.13995/j.cnki.11-1802/ts.023539

Abstract

3,4-Dihydroxylphenylalanine (L-DOPA) is an analog of L-tyrosine (L-Tyr), which has broad application prospects in clinical medicine, cosmetic, health care and other fields. A gene (srth) encoding a tyrosine 3-monooxygenase from Streptosporangium roseum DSM 43021 was cloned and expressed in Bacillus licheniformis, and the recombinant srth was obtained. The intracellular and extracellular activities of the recombinant tyrosine 3-monooxygenase were 30.7 U/mL and 22.79 U/mL, respectively. The recombinant srth and a strain expressed sepiapterin reductase were efficiently used for production of L-DOPA from L-Tyr by whole-cell biotransformation. Tetrahydrobiopterin (BH4) was found a restrictive factor in the process and the ratio of the consumption of L-Tyr to the demand of BH4 was about 1∶2. The results provide a novel biotransformation routine for L-DOPA preparation.

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