Yurimoto Hiroya, Hirai Reiko, Yasueda Hisashi, Mitsui Ryoji, Sakai Yasuyoshi, Kato Nobuo
Division of Applied Life Sciences, Kyoto University, Kitashirakawa, Sakyo-ku, Kyoto 606-8502, Japan.
FEMS Microbiol Lett. 2002 Sep 10;214(2):189-93. doi: 10.1111/j.1574-6968.2002.tb11345.x.
The hps and phi genes encoding 3-hexulose-6-phosphate synthase and 6-phospho-3-hexuloisomerase, the key enzymes of the ribulose monophosphate (RuMP) pathway for formaldehyde fixation, were cloned from the chromosomal DNA of a thermotolerant methylotroph, Bacillus brevis S1. Enzyme induction and Northern blot analyses revealed that both the hps and phi genes are induced by methanol or ethanol, and that their expression is controlled polycistronically at the transcription stage. Sequence analysis also suggested that the hps and phi genes constitute an RuMP operon. The gene organization of the RuMP operon and its surrounding region are unique among bacteria possessing the RuMP pathway genes.
从耐热甲基营养菌短短芽孢杆菌S1的染色体DNA中克隆了编码3-己酮糖-6-磷酸合酶和6-磷酸-3-己酮糖异构酶的hps和phi基因,这两种酶是用于固定甲醛的磷酸戊糖(RuMP)途径的关键酶。酶诱导和Northern印迹分析表明,hps和phi基因均由甲醇或乙醇诱导,并且它们的表达在转录阶段受到多顺反子控制。序列分析还表明,hps和phi基因构成一个RuMP操纵子。RuMP操纵子及其周围区域的基因组织在拥有RuMP途径基因的细菌中是独特的。