Rosson R A, Rittenberg S C
J Bacteriol. 1981 Apr;146(1):108-16. doi: 10.1128/jb.146.1.108-116.1981.
Bdellovibrio bacteriovorus grown axenically or intraperiplasmically on Escherichia coli has pathways for the interconversion of pyrimidines and the synthesis of pyrimidine nucleoside 5'-triphosphates similar to those found in the enteric bacteria. Minimal differences in enzyme activities were observed for axenically and intraperiplasmically grown cells. As might be expected for an organism which takes up deoxyribonucleoside 5'-monophosphates per se, high levels of enzymes which catalyze the generation of deoxyribonucleoside triphosphates from monophosphates were found. In addition, all enzymes of the thymine salvage pathway, except for thymidine kinase, were directly demonstrated in wild-type strains. It was possible to demonstrate this activity only indirectly owing to an inhibitor in wild-type extracts. Investigations with inhibitors of pyrimidine interconversion reactions showed that essentially all B. bacteriovorus deoxyribonucleic acid not synthesized from units derived from E. coli deoxyribonucleic acid is made from components of the substrate organism's ribonucleic acid. Evidence for de novo pyrimidine synthesis from the amino acid level was not found for B. bacteriovorus grown on E. coli that had a high protein/deoxyribonucleic acid ratio or on normal E. coli. The potential for de novo pyrimidine synthesis by intraperiplasmically grown B. bacteriovorus, however, cannot be totally ruled out on the basis of these investigations.
在大肠杆菌上无菌培养或周质内生长的食菌蛭弧菌具有嘧啶相互转化途径以及嘧啶核苷5'-三磷酸的合成途径,这与肠道细菌中的途径相似。对于无菌培养和周质内生长的细胞,观察到酶活性的差异极小。正如预期的那样,对于一种本身摄取脱氧核糖核苷5'-单磷酸的生物体,发现了催化从单磷酸生成脱氧核糖核苷三磷酸的高水平酶。此外,在野生型菌株中直接证明了除胸苷激酶外胸腺嘧啶补救途径的所有酶。由于野生型提取物中的一种抑制剂,只能间接证明这种活性。对嘧啶相互转化反应抑制剂的研究表明,基本上所有不是由源自大肠杆菌脱氧核糖核酸的单位合成的食菌蛭弧菌脱氧核糖核酸都是由底物生物体核糖核酸的成分制成的。对于在蛋白质/脱氧核糖核酸比率高的大肠杆菌上生长的食菌蛭弧菌或在正常大肠杆菌上生长的食菌蛭弧菌,未发现从氨基酸水平从头合成嘧啶的证据。然而,基于这些研究,不能完全排除周质内生长的食菌蛭弧菌从头合成嘧啶的可能性。