Kossmann J, Klintworth R, Bowien B
Institut für Mikrobiologie, Georg-August-Universität Göttingen, F.R.G.
Gene. 1989 Dec 21;85(1):247-52. doi: 10.1016/0378-1119(89)90490-3.
Two DNA fragments encoding the chromosomal and plasmid copies of the gene (cfxP) encoding phosphoribulokinase (PRK) from the chemoautotrophic bacterium Alcaligenes eutrophus, were sequenced and found to be highly homologous. The gene (cfxF) of another Calvin cycle enzyme, fructose-1,6-bisphosphatase (FBPase), was identified as terminating immediately upstream of cfxP, but was not completely contained on both fragments. A hypothetical, also incompletely contained, open reading frame starts closely downstream from cfxP. Genes cfxF, cfxP, and the third hypothetical gene seem to belong to the same operon. The cfxP genes encode highly homologous PRK isoenzyme subunits consisting of 292 aa residues with calculated Mrs of 33 319 (chromosomal PRKc) and 33 164 (plasmid-encoded PRKp). There is little overall sequence similarity between the bacterial and plant (spinach) PRK, apart from some structural motifs.
对来自化能自养细菌嗜碱假单胞菌(Alcaligenes eutrophus)中编码磷酸核糖激酶(PRK)的基因(cfxP)的染色体拷贝和质粒拷贝的两个DNA片段进行了测序,发现它们高度同源。另一种卡尔文循环酶果糖-1,6-二磷酸酶(FBPase)的基因(cfxF)被确定在cfxP上游紧邻处终止,但并未完全包含在这两个片段中。一个假定的、同样未完全包含的开放阅读框在cfxP下游紧邻处开始。基因cfxF、cfxP和第三个假定基因似乎属于同一个操纵子。cfxP基因编码高度同源的PRK同工酶亚基,由292个氨基酸残基组成,计算得出的分子量分别为33319(染色体PRKc)和33164(质粒编码的PRKp)。除了一些结构基序外,细菌和植物(菠菜)的PRK之间几乎没有整体序列相似性。