Marcus M, Halpern Y S
J Bacteriol. 1967 Apr;93(4):1409-15. doi: 10.1128/jb.93.4.1409-1415.1967.
The location of the Escherichia coli K-12 genes determining or regulating glutamate transport, and the location of the gene determining glutamate decarboxylase synthesis, were established by conjugation. The ability to grow on glutamate as the sole source of carbon and energy was used to select for glutamate transport recombinants. Two genes determining the ability to grow on glutamate as the sole source of carbon and energy were mapped. One (gltC) is located near mtl (mannitol), and the other (gltH) appears to be located between the gal (galactose) and trp (tryptophan) loci. The glutamate decarboxylase gene (gad) is strongly linked to gltC. The gltC(+) recombinants grow on glutamate much faster and accumulate this amino acid to a greater extent than do the gltH(+) recombinants. The gltH(+) gene functioned only in one female strain (P678), whereas the gltC gene functioned in all the female strains tested (P678, C600, W1).
通过接合作用确定了大肠杆菌K - 12中决定或调节谷氨酸转运的基因位置,以及决定谷氨酸脱羧酶合成的基因位置。利用以谷氨酸作为唯一碳源和能源生长的能力来筛选谷氨酸转运重组体。定位了两个决定以谷氨酸作为唯一碳源和能源生长能力的基因。一个基因(gltC)位于mtl(甘露醇)附近,另一个基因(gltH)似乎位于gal(半乳糖)和trp(色氨酸)基因座之间。谷氨酸脱羧酶基因(gad)与gltC紧密连锁。与gltH(+)重组体相比,gltC(+)重组体在谷氨酸上生长得更快,并且能积累更多的这种氨基酸。gltH(+)基因仅在一个雌性菌株(P678)中起作用,而gltC基因在所有测试的雌性菌株(P678、C600、W1)中均起作用。