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首页> 外文期刊>Journal of Clinical Microbiology >Rapid, inexpensive method for specific detection of microbial beta-lactamases by detection of fluorescent end products.
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Rapid, inexpensive method for specific detection of microbial beta-lactamases by detection of fluorescent end products.

机译:通过检测荧光终产物,快速,廉价地特异性检测微生物β-内酰胺酶的方法。

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摘要

A rapid method was developed for specific detection of microbial beta-lactamases which uses ampicillin and cephalexin as substrates. The end products (open beta-lactam ring forms) generated after separately incubating either substrate with beta-lactamase-producing organisms initially were separated from the unhydrolyzed substrates by high-voltage electrophoresis at pH 2.1. The end products of both antibiotics were highly fluorescent and could be analyzed visually and semiquantitatively under a long-wave UV lamp. Application of 5 microliters of the same incubation mixture onto filter paper without subsequent electrophoretic separation also resulted in development of fluorescence after brief heating at 120 degrees C for 5 min. This spot test differentiates penicillinase activity from cephalosporinase activity and distinguishes between beta-lactamase and acylase activities, since the end products of acylase [the common side chain, D(-)-alpha-aminophenylacetic acid, and the intact beta-lactam nuclei, 6-aminopenicillanic acid and 7-aminodeacetoxycephalosporanic acid] are not fluorescent. This method was relatively rapid, inexpensive, and more sensitive than the chromogenic cephalosporin (nitrocefin) method when 21 strains of 7 gram-positive species and 77 strains of 29 gram-negative species of bacteria were tested.
机译:开发了一种快速检测微生物β-内酰胺酶的快速方法,该方法使用氨苄青霉素和头孢氨苄作为底物。首先将任一底物与产生β-内酰胺酶的生物体分别孵育后产生的最终产物(开放的β-内酰胺环形式)通过pH值为2.1的高压电泳从未水解的底物中分离出来。两种抗生素的最终产品均具有高荧光性,可以在长波紫外灯下进行目测和半定量分析。在不随后进行电泳分离的情况下,将5微升相同的培养混合物应用到滤纸上,也导致在120摄氏度短暂加热5分钟后产生荧光。该斑点测试将青霉素酶活性与头孢菌素酶活性区分开来,并区分了β-内酰胺酶和酰基转移酶活性,因为酰基转移酶的终产物是[共同侧链D(-)-α-氨基苯基乙酸和完整的β-内酰胺核6 -氨基青霉酸和7-氨基脱乙酰氧基头孢菌酸]不发荧光。当测试21株7克阳性菌种和77株29克阴性菌种时,该方法相对于发色头孢菌素(硝基cefin)方法相对快速,便宜且灵敏。

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