Yow Geok-Yong, Uo Takuma, Yoshimura Tohru, Esaki Nobuyoshi
Institute for Chemical Research, Kyoto University, Gokasho, Uji, 611-0011, Kyoto-fu, Japan.
Arch Microbiol. 2006 Mar;185(1):39-46. doi: 10.1007/s00203-005-0060-x. Epub 2005 Dec 14.
Saccharomyces cerevisiae is sensitive to D-amino acids: those corresponding to almost all proteinous L-amino acids inhibit the growth of yeast even at low concentrations (e.g. 0.1 mM). We have determined that D-amino acid-N-acetyltransferase (DNT) of the yeast is involved in the detoxification of D-amino acids on the basis of the following findings. When the DNT gene was disrupted, the resulting mutant was far less tolerant to D-amino acids than the wild type. However, when the gene was overexpressed with a vector plasmid p426Gal1 in the wild type or the mutant S. cerevisiae as a host, the recombinant yeast, which was found to show more than 100 times higher DNT activity than the wild type, was much more tolerant to D-amino acids than the wild type. We further confirmed that, upon cultivation with D-phenylalanine, N-acetyl-D-phenylalanine was accumulated in the culture but not in the wild type and hpa3Delta cells overproducing DNT cells. Thus, D-amino acids are toxic to S. cerevisiae but are detoxified with DNT by N-acetylation preceding removal from yeast cells.
酿酒酵母对D - 氨基酸敏感:几乎所有蛋白质中的L - 氨基酸对应的D - 氨基酸即使在低浓度(例如0.1 mM)下也会抑制酵母生长。基于以下发现,我们确定酵母的D - 氨基酸 - N - 乙酰转移酶(DNT)参与D - 氨基酸的解毒过程。当DNT基因被破坏时,产生的突变体对D - 氨基酸的耐受性远低于野生型。然而,当该基因在野生型或突变型酿酒酵母作为宿主的情况下用载体质粒p426Gal1进行过表达时,发现重组酵母的DNT活性比野生型高100倍以上,其对D - 氨基酸的耐受性也比野生型高得多。我们进一步证实,在用D - 苯丙氨酸培养时,N - 乙酰 - D - 苯丙氨酸在培养物中积累,但在野生型和过量表达DNT的hpa3Delta细胞中不积累。因此,D - 氨基酸对酿酒酵母有毒,但在从酵母细胞中去除之前,通过DNT进行N - 乙酰化作用使其解毒。