Wilhelm K, Rüger W
Arbeitsgruppe Molekulare Genetik, Lehrstuhl Biologie der Mikroorganismen, Ruhr-Universität Bochum, FRG.
Virology. 1992 Aug;189(2):640-6. doi: 10.1016/0042-6822(92)90587-f.
Phage SPO1 of Bacillus subtilis carries hydroxymethyl-deoxyuridylate in place of thymidylate in its DNA. The enzyme, responsible for the conversion of dUMP to HmdUMP, is a dUMP hydroxymethylase, encoded by the SPO1 gene 29. Here we describe the cloning and sequencing of the gene and the overexpression of the gene product. DNA hybridization using the DNA of bacteriophage T4 dCMP-hydroxymethylase gene as a probe, allowed us to identify and map g29 on a 3.9-kb restriction fragment, EcoRI*11. We determined the nucleotide sequence. One of the open reading frames detected, coding for a putative 44.6-kDa protein, showed significant amino acid homologies with all known thymidylate synthases. Gp29 was overexpressed in the pT7 system. Extracts prepared from induced cells show hydroxymethylase activity in a tritium release assay.
枯草芽孢杆菌的噬菌体SPO1在其DNA中携带羟甲基脱氧尿苷酸而非胸苷酸。负责将dUMP转化为HmdUMP的酶是一种dUMP羟甲基化酶,由SPO1基因29编码。在此,我们描述了该基因的克隆、测序以及基因产物的过表达。使用噬菌体T4 dCMP - 羟甲基化酶基因的DNA作为探针进行DNA杂交,使我们能够在一个3.9 kb的限制性片段EcoRI*11上鉴定并定位g29。我们测定了核苷酸序列。检测到的一个开放阅读框编码一种推定的44.6 kDa蛋白质,与所有已知的胸苷酸合酶显示出显著的氨基酸同源性。Gp29在pT7系统中过表达。从诱导细胞制备的提取物在氚释放测定中显示出羟甲基化酶活性。