Total biosynthesis of hydrocortisone from a simple carbon source in yeast

被引:237
作者
Szczebara, FM
Chandelier, C
Villeret, C
Masurel, A
Bourot, S
Duport, C
Blanchard, S
Groisillier, A
Testet, E
Costaglioli, P
Cauet, G
Degryse, E
Balbuena, D
Winter, J
Achstetter, T
Spagnoli, R
Pompon, D
Dumas, B
机构
[1] Avemtis Pharma, Funct Genom, F-93400 Vitry Sur Seine, France
[2] CNRS, Lab Ingn Prot Membranaires, CGM, F-91198 Gif Sur Yvette, France
[3] Univ Bordeaux 2, Ecole Super Tecnol Biomol Bordeux 2, F-33076 Bordeaux, France
[4] Transgene SA, F-67082 Strasbourg, France
[5] Aventis Pharma, Lead Discovery Technol, F-93235 Romainville, France
关键词
D O I
10.1038/nbt775
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We report on the production of hydrocortisone, the major adrenal glucocorticoid of mammals and an important intermediate of steroidal drug synthesis, from a simple carbon source by recombinant Saccharomyces cerevisiae strains. An artificial and fully self-sufficient biosynthetic pathway involving 13 engineered genes was assembled and expressed in a single yeast strain. Endogenous sterol biosynthesis was rerouted to produce compatible sterols to serve as substrates for the heterologous part of the pathway. Biosynthesis involves eight mammalian proteins (mature forms of CYP11A1, adrenodoxin (ADX), and adrenodoxin reductase (ADR); mitochondrial forms of ADX and CYP11B1; 3beta-HSD, CYP17A1, and CYP21A1). Optimization involved modulating the two mitochondrial systems and disrupting of unwanted side reactions associated with ATF2, GCY1, and YPR1 gene products. Hydrocortisone was the major steroid produced. This work demonstrates the feasibility of transfering a complex biosynthetic pathway from higher eukaryotes into microorganisms.
引用
收藏
页码:143 / 149
页数:7
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