Austin S, Henderson N, Dixon R
Agriculture and Food Research Council Institute of Plant Science Research, University of Sussex, Brighton, England.
Eur J Biochem. 1990 Jan 26;187(2):353-60. doi: 10.1111/j.1432-1033.1990.tb15312.x.
Transcriptional activation by the Klebsiella pneumoniae nitrogen-fixation-specific positive control protein, NIFA, (nifA gene product) has been demonstrated in vitro in S30 extracts from cells which overproduce this protein. The activity of NIFA was dramatically reduced in vitro in the presence of the negative regulatory protein NIFL (nifL gene product) but was not inhibited by the presence of a mutant NIFL protein, NIFL2404. Transcriptional activation from the nifH promoter by NIFA was dependent on the alternative sigma factor, sigma 54, and also required the presence of an upstream activator sequence. NIFA activity was temperature-sensitive in vitro (as it is in vivo) which is due, at least in part, to the intrinsic lability of the protein itself. The majority of overproduced NIFA and NIFL was insoluble after low-speed centrifugation and was inactive in vitro. A low level of less aggregated NIFA protein present in cell extracts was responsible for in vitro activity and this fraction was partially purified.
肺炎克雷伯菌固氮特异性正调控蛋白NIFA(nifA基因产物)的转录激活已在体外过量产生该蛋白的细胞的S30提取物中得到证实。在负调控蛋白NIFL(nifL基因产物)存在的情况下,NIFA的活性在体外显著降低,但不受突变型NIFL蛋白NIFL2404存在的抑制。NIFA对nifH启动子的转录激活依赖于替代sigma因子sigma 54,并且还需要上游激活序列的存在。NIFA活性在体外对温度敏感(如同在体内一样),这至少部分是由于该蛋白质本身固有的不稳定性。大多数过量产生的NIFA和NIFL在低速离心后不溶,并且在体外无活性。细胞提取物中存在的低水平较少聚集的NIFA蛋白负责体外活性,并且该部分已被部分纯化。