Iida T, Sumita T, Ohta A, Takagi M
Department of Biotechnology, University of Tokyo, Yayoi, Bunkyo-ku, Tokyo 113-8657, Japan.
Yeast. 2000 Sep 15;16(12):1077-87. doi: 10.1002/1097-0061(20000915)16:12<1077::AID-YEA601>3.0.CO;2-K.
Genes encoding cytochromes P450 of the CYP52 family in the n-alkane-assimilating yeast Yarrowia lipolytica have been cloned and analyzed. Degenerate PCR primers which were designed for the conserved amino acid sequences of cytochromes P450ALK of Candida species were used for amplification and isolation of genes encoding P450ALK from a genomic DNA library of Y. lipolytica CX161-1B. Seven new genes (YlALK2-YlALK8) were isolated. Five of the seven YlALK genes were induced by n-alkane under the culture conditions used in this study, whereas their expression was strictly repressed by glycerol but not by glucose, similar to the case of YlALK1, reported previously. Disruption of YlALK2, YlALK3, YlALK4 or YlALK6 did not change the growth of Y. lipolytica on medium containing n-alkanes of various chain lengths. A mutant with disruptions in both YlALK1 and YlALK2 did not grow well on n-hexadecane, whereas one with disruptions in both YlALK1 and YlALK3, which has the same phenotype as the YlALK1 singly disrupted mutant, grew well on n-hexadecane. These results suggest that the presence of multiple P450ALK species is a rather common phenomenon among the n-alkane-assimilating yeasts and that in the n-alkane assimilation of Y. lipolytica, YlALK1 functions to assimilate n-decane and longer molecules, whereas YlALK2 is involved in the assimilation of molecules longer than n-dodecane; other YlALKs are not significantly involved in the assimilation of C10-C16 n-alkanes.
已对正烷烃同化酵母解脂耶氏酵母中CYP52家族细胞色素P450的编码基因进行了克隆和分析。根据假丝酵母属细胞色素P450ALK的保守氨基酸序列设计的简并PCR引物,用于从解脂耶氏酵母CX161-1B的基因组DNA文库中扩增和分离编码P450ALK的基因。分离出了7个新基因(YlALK2 - YlALK8)。在本研究使用的培养条件下,7个YlALK基因中的5个受正烷烃诱导,而它们的表达受到甘油的严格抑制,但不受葡萄糖的抑制,这与之前报道的YlALK1的情况类似。破坏YlALK2、YlALK3、YlALK4或YlALK6不会改变解脂耶氏酵母在含有各种链长正烷烃的培养基上的生长情况。YlALK1和YlALK2均被破坏的突变体在正十六烷上生长不佳,而YlALK1和YlALK3均被破坏的突变体(其表型与单独破坏YlALK1的突变体相同)在正十六烷上生长良好。这些结果表明,多种P450ALK种类的存在在正烷烃同化酵母中是一种相当普遍的现象,并且在解脂耶氏酵母的正烷烃同化过程中,YlALK1负责同化正癸烷及更长的分子,而YlALK2参与同化碳链长度大于正十二烷的分子;其他YlALKs在C10 - C16正烷烃的同化过程中没有显著作用。