Abstract
Cell envelopes of Chromobacterium violaceum were isolated and treated under controlled conditions with trypsin, Pronase, lipase, phospholipase C, lysozyme, and a mixture of enzymes produced by a bacteriolytic Pseudomonas sp. After each enzyme treatment, losses in dry weight, protein, lipid, carbohydrate, 2,6-diaminopimelic acid, and total phosphorus were determined. Electron-microscopic examination of the enzyme-treated envelopes indicated complete or partial loss of envelope rigidity or some envelope fragmentation, or both. Each enzyme hydrolyzed at least one envelope component and liberated several others into the supernatant fluid, where they appeared as nondialyzable particulate components, identified by means of electron microscopy. Unlike the other enzymes, the Pseudomonas sp. enzyme mixture partially liberated all major envelope components except phosphorus, heptose, and 2-keto-3-deoxy octonic acid. In spite of these large losses, the envelopes preserved some features of their integrity and elongated shape.
MeSH Terms
Bacterial Proteins/analysis
Carbohydrates/analysis
Cell Membrane/analysis,drug effects
Cell Wall/analysis,drug effects
Chromobacterium/analysis,cytology
Enzymes/pharmacology
Lipase/pharmacology
Lipids/analysis
Microscopy, Electron
Muramidase/pharmacology
Phospholipases/pharmacology
Pimelic Acids/analysis
Trypsin/pharmacology
Chemicals
Bacterial Proteins
Carbohydrates
Enzymes
Lipids
Pimelic Acids
Phospholipases
Lipase
Muramidase
Trypsin
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Whiteside T L
Corpe W A
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