Kahler A E, Switzer R L
Department of Biochemistry, University of Illinois, Urbana 61801, USA.
J Bacteriol. 1996 Aug;178(16):5013-6. doi: 10.1128/jb.178.16.5013-5016.1996.
An in-frame deletion in the coding region of a gene of previously unidentified function (which is called orf2 and which we propose to rename pyrDII) in the Bacillus subtilis pyr operon led to pyrimidine bradytrophy, markedly reduced dihydroorotate dehydrogenase activity, and derepressed levels of other enzymes of pyrimidine biosynthesis. The deletion mutation was not corrected by a plasmid encoding pyrDI, the previously identified gene encoding dihydroorotate dehydrogenase, but was complemented by a plasmid encoding pyrDII. We propose that pyrDII encodes a protein subunit of dihydroorotate dehydrogenase that catalyzes electron transfer from the pyrDI-encoded subunit to components of the electron transport chain.
枯草芽孢杆菌嘧啶操纵子中一个功能此前未明确的基因(称为orf2,我们建议将其重新命名为pyrDII)编码区的框内缺失,导致嘧啶营养缺陷、二氢乳清酸脱氢酶活性显著降低以及嘧啶生物合成中其他酶的去阻遏水平。该缺失突变不能被编码pyrDI(先前鉴定的编码二氢乳清酸脱氢酶的基因)的质粒校正,但能被编码pyrDII的质粒互补。我们提出,pyrDII编码二氢乳清酸脱氢酶的一个蛋白质亚基,该亚基催化电子从pyrDI编码的亚基转移至电子传递链的组分。