Alvarez Vanessa, Rodríguez-Sáiz Marta, de la Fuente Juan Luis, Gudiña Eduardo J, Godio Ramiro P, Martín Juan F, Barredo José Luis
R&D Biology, Antibióticos S.A., Avenida de Antibióticos 59-61, 24009 León, Spain.
Fungal Genet Biol. 2006 Apr;43(4):261-72. doi: 10.1016/j.fgb.2005.12.004. Epub 2006 Feb 7.
The conversion of beta-carotene into xanthophylls is a subject of great scientific and industrial interest. We cloned the crtS gene involved in astaxanthin biosynthesis from two astaxanthin producing strains of Xanthophyllomyces dendrorhous: VKPM Y2410, an astaxanthin overproducing strain, and the wild type ATCC 24203. In both cases, the ORF has a length of 3166 bp, including 17 introns, and codes for a protein of 62.6 kDa with similarity to cytochrome-P450 hydroxylases. crtS gene sequences from strains VKPM Y2410, ATCC 24203, ATCC 96594, and ATCC 96815 show several nucleotide changes, but none of them causes any amino acid substitution, except a G2268 insertion in the 13th exon of ATCC 96815 which causes a change in the reading frame. A G1470 --> A change in the 5' splicing region of intron 8 was also found in ATCC 96815. Both point mutations explain astaxanthin idiotrophy and beta-carotene accumulation in ATCC 96815. Mutants accumulating precursors of the astaxanthin biosynthetic pathway were selected from the parental strain VKPM Y2410 (red) showing different colors depending on the compound accumulated. Two of them were blocked in the biosynthesis of astaxanthin, M6 (orange; 1% astaxanthin, 71 times more beta-carotene) and M7 (orange; 1% astaxanthin, 58 times more beta-carotene, 135% canthaxanthin), whereas the rest produced lower levels of astaxanthin (5-66%) than the parental strain. When the crtS gene was expressed in M7, canthaxanthin accumulation disappeared and astaxanthin production was partially restored. Moreover, astaxanthin biosynthesis was restored when X. dendrorhous ATCC 96815 was transformed with the crtS gene. The crtS gene was heterologously expressed in Mucor circinelloides conferring to this fungus an improved capacity to synthesize beta-cryptoxanthin and zeaxanthin, two hydroxylated compounds from beta-carotene. These results show that the crtS gene is involved in the conversion of beta-carotene into xanthophylls, being potentially useful to engineer carotenoid pathways.
β-胡萝卜素向叶黄素的转化是一个具有重大科学和工业意义的课题。我们从两种产虾青素的树状黄质菌(Xanthophyllomyces dendrorhous)菌株中克隆了参与虾青素生物合成的crtS基因:VKPM Y2410,一种虾青素高产菌株,以及野生型ATCC 24203。在这两种情况下,开放阅读框长度为3166 bp,包括17个内含子,编码一个62.6 kDa的蛋白质,与细胞色素P450羟化酶具有相似性。来自VKPM Y2410、ATCC 24203、ATCC 96594和ATCC 96815菌株的crtS基因序列显示出几个核苷酸变化,但除了ATCC 96815第13外显子中的G2268插入导致阅读框改变外,没有一个导致任何氨基酸替换。在ATCC 96815中还发现了内含子8的5'剪接区域中的G1470→A变化。这两个点突变解释了ATCC 96815中的虾青素营养缺陷和β-胡萝卜素积累。从亲本菌株VKPM Y2410(红色)中筛选出积累虾青素生物合成途径前体的突变体,根据积累的化合物不同呈现出不同颜色。其中两个在虾青素生物合成中受阻,M6(橙色;1%虾青素,β-胡萝卜素含量高71倍)和M7(橙色;1%虾青素,β-胡萝卜素含量高58倍,角黄素含量高135%),而其余突变体产生的虾青素水平(5-66%)低于亲本菌株。当crtS基因在M7中表达时,角黄素积累消失,虾青素产量部分恢复。此外,用crtS基因转化树状黄质菌ATCC 96815时,虾青素生物合成得以恢复。crtS基因在卷枝毛霉(Mucor circinelloides)中异源表达,赋予该真菌合成β-隐黄质和玉米黄质这两种来自β-胡萝卜素的羟基化化合物的能力增强。这些结果表明,crtS基因参与β-胡萝卜素向叶黄素的转化,对工程改造类胡萝卜素途径可能具有重要作用。