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[Peculiarities of Proteus mirabilis extracellular metalloproteinase biosynthesis]
Abstract:
Biosynthesis of metalloproteinase by the Proteus mirabilis 5127-1 strain on different media and the influence of glucose and urea on biosynthesis were studied. It was found that the P. mirabilis 5127-1 bacteria secretes metalloproteinase in the medium in two isoforms (52 and 50 kDa). It was established that proteinase synthesis is completely suppressed during the growth of bacteria on synthetic media, as well as in the presence of LB glucose in the medium. It was demonstrated that addition of urea in the medium results in an increase of the culture productivity in the proteinase synthesis. Maximal culture productivity in the proteinase synthesis was found in the medium with natural urine. During the growth of bacteria on artificial urine, proteinase appeared in the medium only after 12 hours of growth as a single isoform.
Insights
Proteus mirabilis bacteria secrete metalloproteinase, but glucose suppresses its production. Urea and natural urine enhance metalloproteinase (proteinase) biosynthesis by this bacteria strain.
Area of Science:
- Microbiology
- Enzymology
- Bacterial Physiology
Background:
- Proteus mirabilis is known to produce various enzymes, including metalloproteinases.
- Understanding the regulation of metalloproteinase biosynthesis is crucial for potential biotechnological applications.
Purpose of the Study:
- To investigate the biosynthesis of metalloproteinase by Proteus mirabilis 5127-1.
- To determine the influence of glucose and urea on metalloproteinase production.
- To identify optimal conditions for metalloproteinase secretion.
Main Methods:
- Culturing Proteus mirabilis 5127-1 on various media (synthetic, LB glucose, artificial urine, natural urine).
- Analyzing bacterial supernatant for metalloproteinase activity and isoforms via SDS-PAGE.
- Quantifying culture productivity in relation to proteinase synthesis.
Main Results:
- Proteus mirabilis 5127-1 secretes metalloproteinase in two isoforms (52 and 50 kDa).
- Proteinase synthesis was completely inhibited by synthetic media and LB glucose.
- Urea addition significantly increased proteinase synthesis, with maximal productivity observed in natural urine.
- Proteinase production in artificial urine was delayed and appeared as a single isoform.
Conclusions:
- Glucose and synthetic media suppress metalloproteinase production in P. mirabilis.
- Urea and natural urine are effective inducers of metalloproteinase biosynthesis.
- The composition of the growth medium critically affects the yield and isoforms of metalloproteinase secreted by P. mirabilis.
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