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酵母哺乳动物 BCRP 基因编码的黄素输出蛋白同源物的表达激活了产黄素酵母 Candida famata 中的维生素 B 生成。

Expression of yeast homolog of the mammal BCRP gene coding for riboflavin efflux protein activates vitamin B production in the flavinogenic yeast Candida famata.

机构信息

Department of Molecular Biology and Biotechnology, Institute of Cell Biology, NAS of Ukraine, Lviv, Ukraine.

Department of Microbiology and Biotechnology, University of Rzeszow, Rzeszow, Poland.

出版信息

Yeast. 2020 Sep;37(9-10):467-473. doi: 10.1002/yea.3470. Epub 2020 Jul 20.

DOI:10.1002/yea.3470
PMID:32401376
Abstract

Candida famata is a representative of a group of so-called flavinogenic yeast species that overproduce riboflavin (vitamin B ) in response to iron limitation. Overproduced riboflavin accumulates in the cultural medium rather than in the cells suggesting existence of the special mechanisms involved in riboflavin excretion. The corresponding protein and gene have not been identified in yeasts. At the same time, the corresponding gene BCRP has been identified in mammal mammary glands. Several homologs of the mammal BCRP gene encoding putative riboflavin efflux protein (excretase) were identified in Debaryomyces hansenii. The closest homolog was expressed under the control of D. hansenii TEF1 promoter in the riboflavin overproducing strain of C. famata. Resulted transformants overexpressed the corresponding gene and produced 1.4- to 1.8-fold more riboflavin as compared with the parental strain. They also were characterized by overexpression of RIB1 and RIB6 genes of riboflavin synthesis and exhibited elevated specific activity of GTP-cyclohydrolase II. Membrane localization of the riboflavin excretase was confirmed by fluorescent microscopy.

摘要

法氏被孢霉是一组所谓黄素生成酵母的代表,它们在铁限制条件下过量产生核黄素(维生素 B )。过量产生的核黄素积累在培养基中而不是细胞中,这表明存在涉及核黄素排泄的特殊机制。在酵母中尚未鉴定出相应的蛋白质和基因。与此同时,在哺乳动物乳腺中已经鉴定出了相应的 BCRP 基因。在汉逊德巴利酵母中鉴定出了几个编码推定的核黄素外排蛋白(外切酶)的哺乳动物 BCRP 基因的同源物。最接近的同源物在产核黄素过量的法氏被孢霉菌株中,受 D. hansenii TEF1 启动子的控制表达。所得转化体过量表达了相应的基因,与亲本菌株相比产生了 1.4 到 1.8 倍的核黄素。它们还表现出核黄素合成的 RIB1 和 RIB6 基因的过表达,并表现出 GTP-环化水解酶 II 的特异性活性升高。通过荧光显微镜证实了核黄素外排酶的膜定位。

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