Pathirana S M, Vance C P, Miller S S, Gantt J S
Department of Plant Biology, University of Minnesota, St. Paul 55108.
Plant Mol Biol. 1992 Nov;20(3):437-50. doi: 10.1007/BF00040603.
Phosphoenolpyruvate carboxylase (PEPC) plays a key role in N2 fixation and ammonia assimilation in legume root nodules. The enzyme can comprise up to 2% of the soluble protein in root nodules. We report here the isolation and characterization of a cDNA encoding the nodule-enhanced form of PEPC. Initially, a 2945 bp partial-length cDNA was selected by screening an effective alfalfa nodule cDNA library with antibodies prepared against root nodule PEPC. The nucleotide sequence encoding the N-terminal region of the protein was obtained by primer-extension cDNA synthesis and PCR amplification. The complete amino acid sequence of alfalfa PEPC was deduced from these cDNA sequences and shown to bear striking similarity to other plant PEPCs. Southern blots of alfalfa genomic DNA indicate that nodule PEPC is a member of a small gene family. During the development of effective root nodules, nodule PEPC activity increases to a level that is 10- to 15-fold greater than that in root and leaf tissue. This increase appears to be the result of increases in amount of enzyme protein and PEPC mRNA. Ineffective nodules have substantially less PEPC mRNA, enzyme protein and activity than do effective nodules. Maximum expression of root nodule PEPC appears to be related to two signals. The first signal is associated with nodule initiation while the second signal is associated with nodule effectiveness. Regulation of root nodule PEPC activity may also involve post-translational processes affecting enzyme activity and/or degradation.
磷酸烯醇式丙酮酸羧化酶(PEPC)在豆科植物根瘤的固氮和氨同化过程中起关键作用。该酶在根瘤中的可溶性蛋白中所占比例可达2%。我们在此报告了编码根瘤增强型PEPC的cDNA的分离和特性分析。最初,通过用针对根瘤PEPC制备的抗体筛选有效的苜蓿根瘤cDNA文库,选择了一个2945 bp的部分长度cDNA。通过引物延伸cDNA合成和PCR扩增获得了编码该蛋白N端区域的核苷酸序列。从这些cDNA序列推导得出苜蓿PEPC的完整氨基酸序列,结果显示它与其他植物PEPC具有显著的相似性。苜蓿基因组DNA的Southern杂交表明,根瘤PEPC是一个小基因家族的成员。在有效根瘤的发育过程中,根瘤PEPC的活性增加到比根和叶组织中高10至15倍的水平。这种增加似乎是酶蛋白和PEPC mRNA数量增加的结果。无效根瘤中的PEPC mRNA、酶蛋白和活性比有效根瘤少得多。根瘤PEPC的最大表达似乎与两个信号有关。第一个信号与根瘤起始有关,而第二个信号与根瘤有效性有关。根瘤PEPC活性的调节也可能涉及影响酶活性和/或降解的翻译后过程。