Richey D P, Lin E C
J Bacteriol. 1972 Nov;112(2):784-90. doi: 10.1128/jb.112.2.784-790.1972.
Wild-type Escherichia coli possesses an inducible permeation system which catalyzes facilitated diffusion of glycerol into the cell. A spectrophotometric method can be used to assess the presence of this mechanism. The structural gene for the facilitator (glpF) and the structural gene for glycerol kinase (glpK) apparently belong to a single operon. The glpF(+) allele permits effective glycerol utilization by the cells, and, at millimolar concentrations of glycerol, cells carrying the glpF(+) allele grow much faster than glpF genotypes. Although the glycerol-scavenging power of the cell depends both on the facilitated entry of the substrate and its subsequent trapping by an adenosine triphosphate-dependent phosphorylation, the two gene products, the facilitator and kinase, function independently. Wild-type Shigella flexneri appears to be glpK(+) but glpF. This organism grows slowly in media at low concentrations of glycerol. When the glpF(+) and glpK(+) alleles of E. coli are inserted into the S. flexneri genome by transduction, the hybrid strain grows rapidly in low glycerol medium. Vice versa, when the glpF and glpK(+) alleles of S. flexneri are incorporated into E. coli, the hybrid strain grows slowly in low glycerol medium.
野生型大肠杆菌拥有一种可诱导的通透系统,该系统催化甘油以易化扩散的方式进入细胞。一种分光光度法可用于评估这种机制的存在。通透酶的结构基因(glpF)和甘油激酶的结构基因(glpK)显然属于一个操纵子。glpF(+)等位基因使细胞能够有效利用甘油,并且在毫摩尔浓度的甘油条件下,携带glpF(+)等位基因的细胞比glpF基因型的细胞生长得快得多。尽管细胞清除甘油的能力既取决于底物的易化进入以及其随后被依赖三磷酸腺苷的磷酸化作用所捕获,但这两种基因产物,即通透酶和激酶,是独立发挥作用的。野生型弗氏志贺菌似乎是glpK(+)但glpF(-)。这种生物体在低浓度甘油的培养基中生长缓慢。当通过转导将大肠杆菌的glpF(+)和glpK(+)等位基因插入弗氏志贺菌基因组时,杂交菌株在低甘油培养基中生长迅速。反之,当将弗氏志贺菌的glpF(-)和glpK(+)等位基因整合到大肠杆菌中时,杂交菌株在低甘油培养基中生长缓慢。