Takada A, Wachi M, Nagai K
Department of Bioengineering, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama, 226-8501, Japan.
Biochem Biophys Res Commun. 1999 Dec 20;266(2):579-83. doi: 10.1006/bbrc.1999.1863.
We found that the hfq::cat mutant strain produced minicells at high frequency. Minicell production by the mutant strain was more prominent in poor media and in the stationary phase than in rich media and in the exponentially growing phase. The amount of the cell division protein FtsZ increased up to two- to threefold of the wild-type cells in the hfq::cat mutant in the stationary phase, while such differences were not observed in the exponentially growing phase. Increased ftsZ mRNA levels were also observed in the hfq::cat mutant in the stationary phase. These results suggest a negative regulatory role of the DNA-, RNA-binding protein Hfq in cell division in the stationary phase.
我们发现hfq::cat突变株能高频产生微细胞。与在丰富培养基和指数生长期相比,突变株产生微细胞在贫养培养基和稳定期更为显著。在稳定期,hfq::cat突变株中细胞分裂蛋白FtsZ的量增加至野生型细胞的两到三倍,而在指数生长期未观察到这种差异。在稳定期的hfq::cat突变株中也观察到ftsZ mRNA水平升高。这些结果表明DNA、RNA结合蛋白Hfq在稳定期细胞分裂中起负调控作用。