Production of the sesquiterpenoid (+)-nootkatone by metabolic engineering of Pichia pastoris

被引:144
作者
Wriessnegger, Tamara [1 ]
Augustin, Peter [1 ]
Engleder, Matthias [2 ]
Leitner, Erich [3 ]
Muller, Monika [4 ]
Kaluzna, Iwona [4 ]
Schurmann, Martin [4 ]
Mink, Daniel [4 ]
Zellnig, Guenther [5 ]
Schwab, Helmut [1 ,2 ]
Pichler, Harald [1 ,2 ]
机构
[1] ACIB, A-8010 Graz, Austria
[2] Graz Univ Technol, Inst Mol Biotechnol, A-8010 Graz, Austria
[3] Graz Univ Technol, Inst Anal Chem & Food Chem, A-8010 Graz, Austria
[4] DSM Innovat Synth BV, NL-6167 RD Geleen, Netherlands
[5] Graz Univ, Inst Plant Sci, A-8010 Graz, Austria
关键词
Pichia pastoris; Metabolic engineering; Membrane protein; Cytochrome P450; Terpenoid; Nootkatone; COENZYME-A REDUCTASE; SACCHAROMYCES-CEREVISIAE; FUNCTIONAL EXPRESSION; PROTEIN-PRODUCTION; IXODES-SCAPULARIS; CALLITROPSIS-NOOTKATENSIS; AMBLYOMMA-AMERICANUM; CYTOCHROME-P450; 2D6; PLEUROTUS-SAPIDUS; CATALYTIC DOMAIN;
D O I
10.1016/j.ymben.2014.04.001
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
The sesquiterpenoid (+)-nootkatone is a highly demanded and highly valued aroma compound naturally found in grapefruit, pummelo or Nootka cypress tree. Extraction of (+)-nootkatone from plant material or its production by chemical synthesis suffers from low yields and the use of environmentally harmful methods, respectively. Lately, major attention has been paid to biotechnological approaches, using cell extracts or whole-cell systems for the production of (+)-nootkatone. In our study, the yeast Pichia pastoris initially was applied as whole-cell biocatalyst for the production of (+)-nootkatone from (+)-valencene, the abundant aroma compound of oranges. Therefore, we generated a strain co-expressing the premnaspirodiene oxygenase of Hyoscyamus muticus (HPO) and the Arabidopsis thaliana cytochrome P450 reductase (CPR) that hydroxylated extracellularly added (+)-valencene. Intracellular production of (+)-valencene by co-expression of valencene synthase from Callitropsis nootkatensis resolved the phase-transfer issues of (+)-valencene. Bi-phasic cultivations of P. pastoris resulted in the production of trans-nootkatol, which was oxidized to (+)-nootkatone by an intrinsic P. pastoris activity. Additional overexpression of a P. pastoris alcohol dehydrogenase and truncated hydroxy-methylglutaryl-CoA reductase (tHmg1p) significantly enhanced the (+)-nootkatone yield to 208 mg L-1 cell culture in bioreactor cultivations. Thus, metabolically engineered yeast P. pastoris represents a valuable, whole-cell system for high-level production of (+)-nootkatone from simple carbon sources. (C) 2014 International Metabolic Engineering Society. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:18 / 29
页数:12
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