Miyahisa Ikuo, Funa Nobutaka, Ohnishi Yasuo, Martens Stefan, Moriguchi Takaya, Horinouchi Sueharu
Department of Biotechnology, Graduate School of Agriculture and Life Sciences, The University of Tokyo, Bunkyo-ku, Tokyo, 113-8657, Japan.
Appl Microbiol Biotechnol. 2006 Jun;71(1):53-8. doi: 10.1007/s00253-005-0116-5. Epub 2005 Aug 18.
(2S)-Flavanones (naringenin and pinocembrin) are key intermediates in the flavonoid biosynthetic pathway in plants. Recombinant Escherichia coli cells containing four genes for a phenylalanine ammonia-lyase, cinnamate/coumarate:CoA ligase, chalcone synthase, and chalcone isomerase, in addition to the acetyl-CoA carboxylase, have been established for efficient production of (2S)-naringenin from tyrosine and (2S)-pinocembrin from phenylalanine. Further introduction of the flavone synthase I gene from Petroselinum crispum under the control of the T7 promoter and the synthetic ribosome-binding sequence in pACYCDuet-1 caused the E. coli cells to produce flavones: apigenin (13 mg/l) from tyrosine and chrysin (9.4 mg/l) from phenylalanine. Introduction into the E. coli cells of the flavanone 3beta-hydroxylase and flavonol synthase genes from the plant Citrus species led to production of flavonols: kaempferol (15.1 mg/l) from tyrosine and galangin (1.1 mg/l) from phenylalanine. The combinatorial biosynthesis of the flavones and flavonols in E. coli is promising for the construction of a library of various flavonoid compounds and un-natural flavonoids in bacteria.
(2S)-黄烷酮(柚皮素和松属素)是植物类黄酮生物合成途径中的关键中间体。已构建了含有苯丙氨酸解氨酶、肉桂酸/香豆酸:辅酶A连接酶、查尔酮合酶和查尔酮异构酶四个基因,以及乙酰辅酶A羧化酶的重组大肠杆菌细胞,用于从酪氨酸高效生产(2S)-柚皮素和从苯丙氨酸高效生产(2S)-松属素。在pACYCDuet-1载体中,在T7启动子和合成核糖体结合序列的控制下,进一步引入来自皱叶欧芹的黄酮合酶I基因,使大肠杆菌细胞能够生产黄酮:从酪氨酸生产芹菜素(13毫克/升),从苯丙氨酸生产白杨素(9.4毫克/升)。将来自柑橘属植物的黄烷酮3β-羟化酶和黄酮醇合酶基因导入大肠杆菌细胞,导致生产黄酮醇:从酪氨酸生产山奈酚(15.1毫克/升),从苯丙氨酸生产高良姜素(1.1毫克/升)。大肠杆菌中黄酮和黄酮醇的组合生物合成有望用于构建细菌中各种类黄酮化合物和非天然类黄酮的文库。