期刊文献+

代谢工程改造大肠杆菌合成酪醇 被引量:3

Metabolic Engineering of Escherichia coli for Tyrosol Synthesis
在线阅读 下载PDF
导出
摘要 酪醇是一种天然存在于橄榄油、酒及绿茶中的酚类化合物。由于酪醇具有抗炎症和抗氧化的生理活性,因此广泛应用于医药、化工等工业领域。传统的酪醇生产方法是化学合成法,但是这些方法存在着工艺复杂、得率低和环境污染等问题。另外,植物中较低的酪醇含量也限制了酪醇的分离纯化工艺研究。因此微生物发酵法生产酪醇研究越来越受到重视。通过在大肠杆菌内异源表达酿酒酵母中的丙酮酸脱羧酶基因ARO10,成功构建了合成酪醇的重组大肠杆菌。通过敲除预苯酸脱水酶编码基因pheA和苯乙醛脱氢酶编码基因feaB,提高了酪醇的合成能力。在最适的培养条件下,过表达ARO10基因的重组菌利用10 g/L葡萄糖作为碳源,发酵48 h酪醇产量可达4.15 mmol/L。研究发现,发酵培养基中外源添加酪氨酸能够提高重组大肠杆菌的酪醇合成能力。同时,研究还发现在大肠杆菌细胞中存在能够催化酪氨酸合成酪醇的前体物质4-羟基苯丙酮酸的酶。为工业水平微生物发酵法合成酪醇提供了思路。 Tyrosol(2-(4-hydroxyphenyl)ethanol)is an attractive phenolic compound that is naturally found in several foods such as olive oil,wines and green tea.Tyrosol has widely used in pharmaceutical,chemical and other industrial fields because of its anti-inflammatory and antioxidant activities.Traditionally,tyrosol is often produced chemically in industrial scale,however complex process,low yield and environmental issues are hampers.On the other hand,it would be hard to purify tyrosol from olive oil at an industrial scale because of its low concentration,absence of effective separation methods.Therefore,biotechnological production of tyrosol has been paid more and more attention.In this study,the phenylpyruvate decarboxylase gene ARO10 was cloned from Saccharomyces cerevisiae and introduced into Escherichia coli to generate a recombinant tyrosol producer.Furthermore,the genes of pheA and feaB encoding prephenate dehydratase and the endogenous phenylacetaldehyde dehydrogenase respectively,were deleted sequentially to improve tyrosol synthesis.Under the optimal fermentation conditions,the recombinant strain overexpressing ARO10 gene produced 4.15 mmol/L tyrosol from 10 g/L glucose in 48 h.Moreover,it shows that adding tyrosine in M9Y medium could increase tyrosol titer.Meanwhile,it also shows that it had several enzymes that converted tyrosine into 4-hydroyvphenylpyruvate.In summary,we successfully engineered a novel metabolic pathway in E.coli capable of producing tyrosol and provided a strategy for microbial tyrosol production in an industrial-scale.
作者 薛宇翔 陈献忠 杨翠 沈微 樊游 XUE Yuxiang;CHEN Xianzhong;YANG Cui;SHEN Wei;FAN You(Key Laboratory of Industrial Biotechnology,Ministry of Education,Jiangnan University,Wuxi 214122,China;School of Biotechnology,Jiangnan University,Wuxi 214122,China)
出处 《食品与生物技术学报》 CAS CSCD 北大核心 2019年第10期152-159,共8页 Journal of Food Science and Biotechnology
基金 中央高校基本科研业务费专项资金项目(JUSRP51611A)
关键词 酪醇 丙酮酸脱羧酶 大肠杆菌 基因敲除 tyrosol pyruvate decarboxylase Escherichia coli gene knockout
  • 相关文献

参考文献2

二级参考文献14

  • 1Datsenko KA, Wanner BL. One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products. Proc Natl Acad Sci USA, 2000, 97(12): 6640-6645.
  • 2Baba T, Ara T, Hasegawa M, et al. Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants: the keio collection. Mol Syst Biol, 2006, 10.1038/msb4100050.
  • 3Bloor AE, Cranenburgh RM. An efficient method of selectable marker gene excision by Xer recombination for gene replacement in bacterial chromosomes. Appl Environ Microbiol, 2006, 72(4): 2520-2525.
  • 4De Mey M, De Maeseneire S, Soetaert W, et al. Minimizing acetate formation in E. coli fermentations. J Ind Microbiol Biotechnol, 2007, 34(11): 689-700.
  • 5Blakely GW, Sherratt DJ. Interactions of the site-specific recombinases XerC and XerD with the recombination site dif. Nucleic Acids Res, 1994, 22(25): 5613-5620.
  • 6Sambrook J, Russell DW. Molecular Cloning: A Laboratory Manual 3^rd Edn. New York: Cold Spring Harbor Laboratory Press, 2001: 1.199-1.122.
  • 7汪莉,王玉民.用Red重组系统快速敲除大肠杆菌aroL和aroK基因[J].军事医学科学院院刊,2007,31(4):308-311. 被引量:10
  • 8杨海麟,王长城,张玲,孙艳,白洁,王武,杨建勋.产胆固醇氧化酶重组大肠杆菌的发酵培养基和诱导条件的优化[J].食品与生物技术学报,2009,28(5):670-674. 被引量:8
  • 9王君明,崔瑛,王峥涛,季莉莉,崔永霞,刘海,王长虹.超氧化物歧化酶参与肝损伤的研究进展[J].中国实验方剂学杂志,2011,17(7):265-269. 被引量:71
  • 10乔宇,丁宏标,闫俊艳,常敏.重组大肠杆菌产普鲁兰酶的高密度发酵工艺研究[J].生物技术进展,2012,2(3):195-200. 被引量:11

共引文献14

同被引文献9

引证文献3

二级引证文献10

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部