Kato J, Suzuki H, Hirota Y
Mol Gen Genet. 1985;200(2):272-7. doi: 10.1007/BF00425435.
A strain of Escherichia coli lacking the entire ponB gene and a strain lacking the proximal part of the ponA gene were constructed by substitution with a drug resistance gene. These strains lost either penicillin-binding protein(PBP)-1b or -1a totally and their growth was apparently normal at 30 degrees C and 42 degrees C except that growth of the ponB deletion strain was poor on a nutrient agar plate containing no NaCl at 30 degrees C as well as at 42 degrees C. Transductional experiments to introduce the ponB deletion into the ponA deletion strain, and vice versa, showed that the ponA ponB double deletion was lethal unless the deletion was functionally compensated, e.g., by the presence of a plasmid carrying either gene. Thus, either PBP-1b (ponB) or PBP-1a (ponA), but not both, is dispensable for cell viability, at least under ordinary culture conditions. Transductional experiments also suggested that the gamma component of PBP-1b or the PBP-1b lacking the C-terminal portion encoded in the distal region to the SphI site on the ponB was sufficient for supporting growth of the E. coli cell.
通过用耐药基因进行替换,构建了一株缺失整个ponB基因的大肠杆菌菌株和一株缺失ponA基因近端部分的菌株。这些菌株分别完全缺失青霉素结合蛋白(PBP)-1b或-1a,并且在30℃和42℃时它们的生长明显正常,只是ponB缺失菌株在30℃和42℃下于不含NaCl的营养琼脂平板上生长较差。将ponB缺失导入ponA缺失菌株以及反之的转导实验表明,除非缺失通过例如携带任一基因的质粒进行功能补偿,否则ponA ponB双缺失是致死的。因此,至少在普通培养条件下,PBP-1b(ponB)或PBP-1a(ponA)中的一种而非两者对于细胞活力是必需的。转导实验还表明,PBP-1b的γ组分或缺失ponB上SphI位点远端区域编码的C末端部分的PBP-1b足以支持大肠杆菌细胞的生长。