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Production of miltiradiene by metabolically engineered Saccharomyces cerevisiae

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논문

Production of miltiradiene by metabolically engineered Saccharomyces cerevisiae

학술지

Biotechnology and bioengineering

저자명

Dai, Zhubo; Liu, Yi; Huang, Luqi; Zhang, Xueli

초록

<P><B>Abstract</B></P><P>Metabolic engineering of microorganisms is an alternative and attractive route for production of valuable terpenoids that are usually extracted from plant sources. Tanshinones are the bioactive components of <I>Salvia miltiorrhizha</I> Bunge, which is a well&#8208;known traditional Chinese medicine widely used for treatment of many cardiovascular diseases. As a step toward microbial production of tanshinones, copalyl diphosphate (CPP) synthase, and normal CPP kaurene synthase&#8208;like genes, which convert the universal diterpenoid precursor geranylgeranyl diphosphate (GGPP) to miltiradiene (an important intermediate of the tanshinones synthetic pathway), was introduced into <I>Saccharomyces cerevisiae</I>, resulting in production of 4.2&thinsp;mg/L miltiradiene. Improving supplies of isoprenoid precursors was then investigated for increasing miltiradiene production. Although over&#8208;expression of a truncated 3&#8208;hydroxyl&#8208;3&#8208;methylglutaryl&#8208;CoA reductase (<I>tHMGR</I>) and a mutated global regulatory factor (<I>upc2.1</I>) gene did improve supply of farnesyl diphosphate (FPP), production of miltiradiene was not increased while large amounts of squalene (78&thinsp;mg/L) were accumulated. In contrast, miltiradiene production increased to 8.8&thinsp;mg/L by improving supply of GGPP through over&#8208;expression of a fusion gene of FPP synthase (<I>ERG20</I>) and endogenous GGPP synthase (<I>BTS1</I>) together with a heterologous GGPP synthase from <I>Sulfolobus acidocaldarius</I> (<I>SaGGPS</I>). Auxotrophic markers in the episomal plasmids were then replaced by antibiotic markers, so that engineered yeast strains could use rich medium to obtain better cell growth while keeping plasmid stabilities. Over&#8208;expressing <I>ERG20&#8208;BTS1</I> and <I>SaGGPS</I> genes increased miltiradiene production from 5.4 to 28.2&thinsp;mg/L. Combinatorial over&#8208;expression of <I>tHMGR&#8208;upc2.1</I> and <I>ERG20&#8208;BTS1&#8208;SaGGPS</I> genes had a synergetic effects on miltiradiene production, increasing titer to 61.8&thinsp;mg/L. Finally, fed&#8208;batch fermentation was performed, and 488&thinsp;mg/L miltiradiene was produced. The yeast strains engineered in this work provide a basis for creating an alternative way for production of tanshinones in place of extraction from plant sources. Biotechnol. Bioeng. 2012; 109: 2845&ndash;2853. &copy; 2012 Wiley Periodicals, Inc.</P>

발행연도

2012

발행기관

Wiley Subscription Services, Inc., A Wiley Company

ISSN

0006-3592

ISSN

1097-0290

109

11

페이지

pp.2845-2853

주제어

tanshinones; miltiradiene; terpenoids; isoprenoid precursors; fermentation; Saccharomyces cerevisiae

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논문; 2012-12-31

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