Bruce D L, Warren R A
J Bacteriol. 1979 Sep;139(3):811-6. doi: 10.1128/jb.139.3.811-816.1979.
Incompatibility group P-1 plasmids with the bla+ genotype were transferred from various Escherichia coli strains to Pseudomonas acidovorans strain 29. When resistance to ampicillin was used as the criterion, none of these plasmids appeared able to express their Bla+ phenotype in this host. When the plasmids were subsequently transferred back from these ampicillin-sensitive P. acdiovorans transcipients to E. coli strains, it was found that the Bla+ phenotype was again expressed. Although beta-lactamase was not detected in cultures of P. acidovorans transcipients, macroiodometric determinations of beta-lactamase activity made on broken cell suspensions revealed that beta-lactamase was indeed synthesized. It was concluded that P. acidovorans strain 29 allows expression of the bla gene within the cell but that this organism is unable to excrete the enzyme.
具有bla+基因型的不相容群P-1质粒从各种大肠杆菌菌株转移至食酸假单胞菌菌株29。以对氨苄西林的抗性作为标准时,这些质粒似乎均无法在该宿主中表达其Bla+表型。当这些质粒随后从这些对氨苄西林敏感的食酸假单胞菌转导子转移回大肠杆菌菌株时,发现Bla+表型再次得以表达。尽管在食酸假单胞菌转导子培养物中未检测到β-内酰胺酶,但对破碎细胞悬液进行的β-内酰胺酶活性的宏观碘量法测定表明,β-内酰胺酶确实得以合成。得出的结论是,食酸假单胞菌菌株29允许细胞内bla基因的表达,但该生物体无法分泌该酶。