Turner G
Department of Molecular Biology and Biotechnology, University of Sheffield, UK.
Ciba Found Symp. 1992;171:113-24; discussion 124-8.
Rapid progress has recently been made in the characterization of genes and gene clusters involved in the biosynthesis of beta-lactam antibiotics such as penicillins, cephalosporins and cephamycins. The biosynthetic pathways are found in a wide range of microorganisms, including fungi, actinomycetes and Gram-negative bacteria. Comparisons of gene sequences (particularly the genes encoding isopenicillin N synthetase) and gene organization in these different microorganisms have led to proposals about the evolution of this group of pathways, and how they might have been transferred from prokaryotes to eukaryotes. The isolation and characterization of the genes encoding ACV (tripeptide) synthetase, the first step in the beta-lactam biosynthetic pathway, have revealed the presence of three partly repeated domains, most likely responsible for the recognition, adenylation and activation of the three amino acid precursors of the penams and cephems. This has confirmed their classification as peptide synthetases, distantly related to enzymes responsible for the synthesis of peptide antibiotics in Bacillus brevis and other bacteria and fungi.
最近,在涉及β-内酰胺抗生素(如青霉素、头孢菌素和头霉素)生物合成的基因和基因簇的表征方面取得了快速进展。生物合成途径存在于多种微生物中,包括真菌、放线菌和革兰氏阴性菌。对这些不同微生物中的基因序列(特别是编码异青霉素N合成酶的基因)和基因组织进行比较,引发了关于这组途径的进化以及它们可能如何从原核生物转移到真核生物的推测。β-内酰胺生物合成途径第一步中编码ACV(三肽)合成酶的基因的分离和表征,揭示了存在三个部分重复的结构域,最有可能负责青霉烷和头孢烯的三种氨基酸前体的识别、腺苷化和活化。这证实了它们作为肽合成酶的分类,与负责短芽孢杆菌和其他细菌及真菌中肽抗生素合成的酶有较远的亲缘关系。