Lopez P, Greenberg B, Lacks S A
Biology Department, Brookhaven National Laboratory, Upton, New York 11973.
J Bacteriol. 1990 Sep;172(9):4766-74. doi: 10.1128/jb.172.9.4766-4774.1990.
A cloned segment of the chromosome of Streptococcus pneumoniae, in which mutations to sulfonamide resistance occur, contains several genes encoding enzymes for folate biosynthesis. Determination of the DNA sequence of parts of this segment and identification of a putative promoter and terminator of transcription indicate an operon composed of four genes. The first, sulA, encodes the enzyme dihydropteroate synthase. The functions of the second and third possible genes, sulB and sulC, are not known. The last gene, sulD, encodes a 6-hydroxymethyl-7,8-dihydropterin pyrophosphokinase. The product of this enzyme is the substrate for dihydropteroate synthetase. The enzyme protein was partially purified and shown to consist of a single subunit of 31 kilodaltons, encoded by sulD. On the basis of gel filtration behavior, the native protein appears to be a trimer or tetramer. Subcloning of the sulD gene in an Escherichia coli expression vector increased expression of the pyrophosphokinase 1,000-fold over the level produced by a single copy of the chromosomal gene.
肺炎链球菌染色体的一个克隆片段中会发生对磺胺类药物的抗性突变,该片段包含几个编码叶酸生物合成酶的基因。对该片段部分区域的DNA序列测定以及对推定的转录启动子和终止子的鉴定表明,这是一个由四个基因组成的操纵子。第一个基因sulA编码二氢蝶酸合酶。另外两个可能的基因sulB和sulC的功能尚不清楚。最后一个基因sulD编码6-羟甲基-7,8-二氢蝶呤焦磷酸激酶。该酶的产物是二氢蝶酸合酶的底物。该酶蛋白经部分纯化后显示由一个31千道尔顿的单亚基组成,由sulD编码。根据凝胶过滤行为,天然蛋白似乎是三聚体或四聚体。将sulD基因亚克隆到大肠杆菌表达载体中,使焦磷酸激酶的表达比染色体基因单拷贝产生的水平提高了1000倍。