Smith I, Paress P, Cabane K, Dubnau E
Mol Gen Genet. 1980;178(2):271-9. doi: 10.1007/BF00270472.
Stringent factor (ATP:GTP-3' pyrophosphotransferase) has been purified from wild type Bacillus subtilis and it has been shown that guanosine tetra- and pentaphosphate (ppGpp and pppGpp) are synthesized in vitro in the presence of ribosomes, unacylated tRNA and its specific codon, as has been demonstrated in Escherichia coli. relA, the genetic determinant for the stringent factor, has been mapped on the B. subtilis chromosome by transduction and is found between aroD and leu. The relC locus, defined by mutations which were originally selected by resistance to thiostrepton, has been mapped adjacent to spoOH in the order cysA, spoOH, relC, rif. Sringent factor and ribosomes are functional for the in vitro synthesis of (p)ppGpp in early stages of sporulation (up to at least 4 h). This contradicts the findings of other laboratories.
严谨因子(ATP:GTP-3'-焦磷酸转移酶)已从野生型枯草芽孢杆菌中纯化出来,并且已表明,如同在大肠杆菌中所证实的那样,在核糖体、未酰化的tRNA及其特定密码子存在的情况下,鸟苷四磷酸和五磷酸(ppGpp和pppGpp)能在体外合成。relA,即严谨因子的遗传决定因素,已通过转导定位在枯草芽孢杆菌染色体上,位于aroD和leu之间。relC位点由最初通过对硫链丝菌素的抗性筛选出的突变所定义,已按cysA、spoOH、relC、rif的顺序定位在spoOH附近。在芽孢形成的早期阶段(至少长达4小时),严谨因子和核糖体对于体外合成(p)ppGpp具有功能。这与其他实验室的发现相矛盾。