Sandmann G, Misawa N
Lehrstuhl für Physiologie und Biochemie der Pflanzen, Universität Konstanz, F.R.G.
FEMS Microbiol Lett. 1992 Jan 15;69(3):253-7. doi: 10.1016/0378-1097(92)90656-9.
The role of carotenoid genes crtB and crtE has been functionally assigned. These genes were cloned from Erwinia into Escherichia coli or Agrobacterium tumefaciens. Their functions were elucidated by assaying early isoprenoid enzymes involved in phytoene formation. In vitro reactions from extracts of E. coli carrying the crtE gene or a complete carotenogenic gene cluster in which crtB was deleted showed an elevated conversion of farnesyl pyrophosphate (FPP) into geranylgeranyl pyrophosphate (GGPP). These results strongly indicate that the crtE gene encodes GGPP synthase. Introduction of the crtB gene into A. tumefaciens led to the conversion of GGPP into phytoene. This activity was absent in similar transformants with the crtE gene. Thus, the crtB gene probably encodes phytoene synthase, which was further supported by demonstration that phytoene accumulated in E. coli harboring both the crtB and crtE genes.
类胡萝卜素基因crtB和crtE的功能已得到明确。这些基因从欧文氏菌克隆到大肠杆菌或根癌农杆菌中。通过检测参与八氢番茄红素形成的早期类异戊二烯酶,阐明了它们的功能。在携带crtE基因的大肠杆菌提取物或缺失crtB的完整类胡萝卜素生成基因簇的体外反应中,法尼基焦磷酸(FPP)向香叶基香叶基焦磷酸(GGPP)的转化率有所提高。这些结果有力地表明,crtE基因编码GGPP合酶。将crtB基因导入根癌农杆菌导致GGPP转化为八氢番茄红素。在携带crtE基因的类似转化体中不存在这种活性。因此,crtB基因可能编码八氢番茄红素合酶,这一点通过在同时携带crtB和crtE基因的大肠杆菌中积累八氢番茄红素得到了进一步支持。