首页|代谢工程改造酿酒酵母生产β-胡萝卜素

代谢工程改造酿酒酵母生产β-胡萝卜素

扫码查看
β-胡萝卜素在食品、药品和化妆品领域有广泛用途.为获得生产β-胡萝卜素的微生物细胞工厂,本研究首先在酿酒酵母BY4742中过表达甲羟戊酸(MVA)途径的限速酶3-羟基-3-甲基戊二酰辅酶A还原酶(HMGR)基因及二萜化合物合成的关键酶牻牛儿基牻牛儿基焦磷酸合酶(GGPS)基因,来提高牻牛儿基牻牛儿基焦磷酸(GGPP)的供给.在酿酒酵母底盘菌BY4742-T2的基础上整合来源于成团泛菌和红法夫酵母的β-胡萝卜素合成基因,比较酿酒酵母工程菌生产β-胡萝卜素的差别.结果表明提高酿酒酵母中HMGR和GGPS酶基因的表达能将工程菌中β-胡萝卜素的产量提高26.0倍.另外,来源于真核生物红法夫酵母的合成基因相比成团泛菌,更有利于酿酒酵母生产β-胡萝卜素.最终获得的酿酒酵母工程菌BW02能生产1.56 mg/g细胞干重的β-胡萝卜素,为进一步获得高产β-胡萝卜素细胞工厂提供基础.
Production of β-carotene by metabolically engineered Saccharomyces cerevisiae
β-carotene has a wide range of application in food,pharmaceutical and cosmetic industries.For microbial production of β-carotene in Saccharomyces cerevisiae,the supply of geranylgeranyl diphosphate (GGPP) was firstly increased in S.cerevisiae BY4742 to obtain strain BY4742-T2 through over-expressing truncated 3-hydroxy-3-methylglutaryl-CoA reductase (tHMGR),which is the major rate-limiting enzyme in the mevalonate (MVA) pathway,and GGPP synthase (GGPS),which is a key enzyme in the diterpenoid synthetic pathway.The β-carotene synthetic genes of Pantoea agglomerans and Xanthophyllomyces dendrorhous were further integrated into strain BY4742-T2 for comparing β-carotene production.Over-expression of tHMGR and GGPS genes led to 26.0-fold increase of β-carotene production.In addition,genes from X.dendrorhous was more efficient than those from P.agglomerans for β-carotene production in S.cerevisiae.Strain BW02 was obtained which produced 1.56 mg/g (dry cell weight) β-carotene,which could be used further for constructing cell factories for β-carotene production.

β-carotenePantoea agglomeransXanthophyllomyces dendrorhousSaccharomyces cerevisiae

王贝贝、施明雨、王冬、许骄阳、刘怡、杨洪江、戴住波、张学礼

展开 >

天津科技大学生物工程学院,天津300457

中国科学院天津工业生物技术研究所,天津300308

中国科学院系统微生物工程重点实验室,天津 300308

β-胡萝卜素 成团泛菌 红法夫酵母 酿酒酵母

国家高技术研究发展计划(863计划)国家自然科学基金国家重点基础研究发展计划(973计划)中国科学院百人计划资助

2012AA02A704812028642011CBA00800

2014

生物工程学报
中国科学院微生物研究所 中国微生物学会

生物工程学报

CSTPCDCSCD北大核心
影响因子:0.641
ISSN:1000-3061
年,卷(期):2014.30(8)
  • 6
  • 2