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β-内酰胺类抗生素的生产及其调控。

Production of beta-lactam antibiotics and its regulation.

作者信息

Demain A L

机构信息

Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.

出版信息

Proc Natl Sci Counc Repub China B. 1991 Oct;15(4):251-65.

PMID:1815263
Abstract

The discovery of penicillin was announced over 60 years ago. It was the first beta-lactam antibiotic and the importance of this group is greater today than it has ever been. It is clear that even at 60 years of age, beta-lactams are going strong and no one contemplates their early retirement. Currently, sales of beta-lactam compounds form the largest share by far of the world's antibiotic market. The beta-lactam antibiotics include penicillins such as penicillin G, penicillin V, ampicillin, cloxacillin, and piperacillin; cephalosporins such as cephalothin, cephaloridine, cephalexin, and cefaclor; and cephamycins such as cefoxitin. In addition, beta-lactam antibiotics include the more recently developed nonclassical structures such as monobactams, including aztreonam; clavulanic acid, which is a component of the combination drug augmentin; and thienamycin, which is chemically transformed into imipenem, a component of the combination drug known as primaxin (or tienam). The classical beta-lactam antibiotics can be divided into hydrophobic and hydrophilic fermentation products. The hydrophobic members, e.g. benzylpenicillin (penicillin G) and phenoxymethylpenicillin (penicillin V), contain non-polar side chains, e.g. phenylacetate and phenoxyacetate, respectively, and are made only by filamentous fungi; the best known of these is Penicillium chrysogenum. The antibacterial spectrum of the hydrophobic penicillins is essentially Gram-positive. The hydrophilic types are penicillin N, cephalosporins and 7-alpha-methoxycephalosporins (cephamycins) which are made by fungi, actinomycetes and unicellular bacteria. They all contain the polar side chain, D-alpha-aminoadipate. We can draw a sequence of reactions which describes the biosynthesis of all penicillins and cephalosporins, however the total sequence exists in no one microorganism. All penicillin and cephalosporin biosynthetic pathways possess the first three steps in common and all cephalosporin pathways go through deacetylcephalosporin C. However, there are many subsequent biosynthetic reactions which vary in the different producing organisms. Production of beta-lactam antibiotics occurs best under conditions of nutrient imbalance and at low growth rates. Nutrient imbalance can be brought about by limitation of the carbon, nitrogen or phosphorus source. In addition to these factors, amino acids such as lysine and methionine exert marked effects on production of penicillins and/or cephalosporins by some microorganisms. Induction of some of the synthetases, especially the first enzyme, ACV synthetase, by methionine is the basis of the methionine stimulation of cephalosporin C synthesis in C. acremonium. Inhibition of homocitrate synthase is the mechanism involved in lysine inhibition of penicillin synthesis in Penicillium chrysogenum.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

青霉素的发现是在60多年前宣布的。它是第一种β-内酰胺抗生素,如今这类抗生素的重要性比以往任何时候都更高。很明显,即便已问世60年,β-内酰胺类抗生素依然强劲,没人会考虑让它们早早“退休”。目前,β-内酰胺类化合物的销售额在全球抗生素市场中所占份额迄今为止是最大的。β-内酰胺抗生素包括青霉素类,如青霉素G、青霉素V、氨苄西林、氯唑西林和哌拉西林;头孢菌素类,如头孢噻吩、头孢利定、头孢氨苄和头孢克洛;以及头霉素类,如头孢西丁。此外,β-内酰胺抗生素还包括最近开发的非经典结构,如单环β-内酰胺类,包括氨曲南;克拉维酸,它是复方制剂奥格门汀的一种成分;以及硫霉素,它经过化学转化成为亚胺培南,亚胺培南是复方制剂普立万星(或泰能)的一种成分。经典的β-内酰胺抗生素可分为疏水性和亲水性发酵产物。疏水性成员,如苄青霉素(青霉素G)和苯氧甲基青霉素(青霉素V),分别含有非极性侧链,如苯乙酸酯和苯氧乙酸酯,并且仅由丝状真菌产生;其中最知名的是产黄青霉。疏水性青霉素的抗菌谱基本上是革兰氏阳性菌。亲水性类型包括青霉素N、头孢菌素和7-α-甲氧基头孢菌素(头霉素),它们由真菌、放线菌和单细胞细菌产生。它们都含有极性侧链D-α-氨基己二酸。我们可以画出一系列反应来描述所有青霉素和头孢菌素的生物合成过程,然而完整的反应序列并不存在于任何一种微生物中。所有青霉素和头孢菌素的生物合成途径都有共同的前三个步骤,并且所有头孢菌素途径都要经过去乙酰头孢菌素C。然而,后续还有许多生物合成反应在不同的生产生物体中有所不同。β-内酰胺抗生素在营养失衡和低生长速率的条件下产量最高。营养失衡可由碳源、氮源或磷源的限制引起。除了这些因素外,赖氨酸和蛋氨酸等氨基酸对某些微生物产生青霉素和/或头孢菌素也有显著影响。蛋氨酸对顶头孢霉中头孢菌素C合成的刺激作用其基础是蛋氨酸对一些合成酶,尤其是第一种酶ACV合成酶的诱导。高柠檬酸合酶的抑制是产黄青霉中赖氨酸抑制青霉素合成所涉及的机制。

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