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编码红酵母虾青素生物合成基因八氢番茄红素去饱和酶的克隆与鉴定

Cloning and characterization of the astaxanthin biosynthetic gene encoding phytoene desaturase of Xanthophyllomyces dendrorhous.

作者信息

Verdoes J C, Misawa N, van Ooyen A J

出版信息

Biotechnol Bioeng. 1999 Jun 20;63(6):750-5. doi: 10.1002/(sici)1097-0290(19990620)63:6<750::aid-bit13>3.0.co;2-7.

Abstract

The first carotenoid biosynthetic gene from the basidiomycetous yeast Xanthophyllomyces dendrorhous was isolated by heterologous complementation in Escherichia coli. The isolated gene, denominated as crtI, was found to encode for phytoene desaturase. The coding region is interrupted by 11 introns. The deduced amino acid sequence showed significant homology with its bacterial and eukaryotic counterparts, especially those of fungal origin. A plasmid containing the geranylgeranyl diphosphate synthase and phytoene synthase encoding genes from Erwinia uredovora was introduced in E. coli together with the phytoene desaturase encoding cDNA from X. dendrorhous. As a result, lycopene accumulation was observed in these transformants. We conclude that in X. dendrorhous the four desaturase steps, by which phytoene is converted into lycopene, are carried out by a single gene product.

摘要

通过在大肠杆菌中的异源互补,首次从担子菌酵母红法夫酵母中分离出类胡萝卜素生物合成基因。分离出的基因命名为crtI,发现其编码八氢番茄红素去饱和酶。编码区被11个内含子中断。推导的氨基酸序列与其细菌和真核对应物,特别是那些真菌来源的对应物具有显著同源性。将含有来自丁香假单胞菌的牻牛儿基牻牛儿基二磷酸合酶和八氢番茄红素合酶编码基因的质粒与来自红法夫酵母的八氢番茄红素去饱和酶编码cDNA一起导入大肠杆菌。结果,在这些转化体中观察到番茄红素积累。我们得出结论,在红法夫酵母中,八氢番茄红素转化为番茄红素的四个去饱和步骤由单一基因产物完成。

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