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β-内酰胺抗生素与链霉菌R39的胞外D-羧肽酶-转肽酶的结合。

Binding of beta-lactam antibiotics to the exocellular DD-carboxypeptidase-transpeptidase of Streptomyces R39.

作者信息

Frère J M, Ghuysen J M, Reynolds P E, Moreno R

出版信息

Biochem J. 1974 Oct;143(1):241-9. doi: 10.1042/bj1430241.

Abstract

Benzylpenicillin and cephaloridine reacted with the exocellular dd-carboxypeptidase-transpeptidase from Streptomyces R39 to form equimolar and inactive antibiotic-enzyme complexes. At saturation, the molar ratio of chromogenic cephalosporin 87-312 to enzyme was 1.3:1, but this discrepancy might be due to a lack of accuracy in the measurement of the antibiotic. Spectrophotometric studies showed that binding of cephaloridine and cephalosporin 87-312 to the enzyme caused opening of their beta-lactam rings. Benzylpenicillin and cephalosporin 87-312 competed for the same site on the free enzyme, suggesting that binding of benzylpenicillin also resulted in the opening of its beta-lactam ring. In Tris-NaCl-MgCl(2) buffer at pH7.7 and 37 degrees C, the rate constants for the dissociation of the antibiotic-enzyme complexes were 2.8x10(-6), 1.5x10(-6) and 0.63x10(-6)s(-1) (half-lives 70, 130 and 300h) for benzylpenicillin, cephalosporin 87-312 and cephaloridine respectively. During the process, the protein underwent reactivation. The enzyme that was regenerated from its complex with benzylpenicillin was as sensitive to fresh benzylpenicillin as the native enzyme. With [(14)C]benzylpenicillin, the released radioactive compound was neither benzylpenicillin nor benzylpenicilloic acid. The Streptomyces R39 enzyme thus behaved as a beta-lactam-antibiotic-destroying enzyme but did not function as a beta-lactamase. Incubation at 37 degrees C in 0.01m-phosphate buffer, pH7.0, and in the same buffer supplemented with sodium dodecyl sulphate caused a more rapid reversion of the [(14)C]benzylpenicillin-enzyme complex. The rate constants were 1.6x10(-5)s(-1) and 0.8x10(-4)s(-1) respectively. Under these conditions, however, there was no concomitant reactivation of the enzyme and the released radioactive compound(s) appeared not to be the same as before. The Streptomyces R39 enzyme and the exocellular dd-carboxypeptidase-transpeptidase from Streptomyces R61 appeared to differ from each other with regard to the topography of their penicillin-binding site.

摘要

苄青霉素和头孢菌素与来自链霉菌R39的胞外D - 羧肽酶 - 转肽酶反应,形成等摩尔且无活性的抗生素 - 酶复合物。在饱和状态下,显色头孢菌素87 - 312与酶的摩尔比为1.3:1,但这种差异可能是由于抗生素测量缺乏准确性所致。分光光度研究表明,头孢菌素和头孢菌素87 - 312与酶的结合导致它们的β - 内酰胺环打开。苄青霉素和头孢菌素87 - 312在游离酶上竞争相同位点,这表明苄青霉素的结合也导致其β - 内酰胺环打开。在pH7.7和37℃的Tris - NaCl - MgCl₂缓冲液中,苄青霉素、头孢菌素87 - 312和头孢菌素的抗生素 - 酶复合物解离的速率常数分别为2.8×10⁻⁶、1.5×10⁻⁶和0.63×10⁻⁶s⁻¹(半衰期分别为70、130和300小时)。在此过程中,蛋白质发生再活化。从其与苄青霉素的复合物中再生的酶对新鲜苄青霉素的敏感性与天然酶相同。用[¹⁴C]苄青霉素时,释放的放射性化合物既不是苄青霉素也不是苄青霉素酸。因此,链霉菌R39酶表现为一种破坏β - 内酰胺抗生素的酶,但不起β - 内酰胺酶的作用。在pH7.0的0.01m磷酸盐缓冲液中于37℃孵育,以及在补充有十二烷基硫酸钠的相同缓冲液中孵育,会使[¹⁴C]苄青霉素 - 酶复合物更快地逆转。速率常数分别为1.6×10⁻⁵s⁻¹和0.8×10⁻⁴s⁻¹。然而,在这些条件下,没有伴随酶的再活化,并且释放的放射性化合物似乎与之前不同。链霉菌R39酶和来自链霉菌R61的胞外D - 羧肽酶 - 转肽酶在其青霉素结合位点的拓扑结构方面似乎彼此不同。

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