A Rapid and Sensitive Assay of Muramidase.
Richard M. Parry, Ramesh C. Chandan, KHEM M. SHAHANI
Abstract
Richard M. Parry, Ramesh C. Chandan, KHEM M. SHAHANI
Abstract
An improved method has been developed for assay of muramidase in several biological systems. This method involves measurement of the rate of lysis of a 25 mg% suspension of M. lysodeikticus in 0.05 M NaCl and M/15 phosphate buffer, pH 6.2. The rate of lysis is measured in a Beckman DB spectrophotometer at 540 mμ with an attached recorder. This modification allows continuous measurement of the initial reaction velocity for samples containing from 0.1 to 10 μg of muramidase.
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An improved method has been developed for assay of muramidase in several biological systems. This method involves measurement of the rate of lysis of a 25 mg% suspension of M. lysodeikticus in 0.05 M NaCl and M/15 phosphate buffer, pH 6.2. The rate of lysis is measured in a Beckman DB spectrophotometer at 540 mμ with an attached recorder. This modification allows continuous measurement of the initial reaction velocity for samples containing from 0.1 to 10 μg of muramidase.
Key concepts: Muramidase, Lysis, Chemistry, Chromatography, Lysozyme, Phosphate buffered saline, Suspension (topology), Biochemistry