Increased yield of a lysozyme after self-cloning of the gene in Streptomyces coelicolor Müller

Streptomyces coelicolor "Müller" DSM3030 excretes a lysozyme comprising both beta-1,4-N-acetyl- and beta-1,4-N,6-O-diacetyl muramidase activities. The lysozyme is named Cellosyl. Gene libraries have been established using genomic DNA from the wild-type strain, S. coelicolor DSM3030, and fr...

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Veröffentlicht in:Applied microbiology and biotechnology 1991, Vol.34 (4), p.481-487
Hauptverfasser: BRAÊU, B, HILGENFELD, R, SCHLINGMANN, M, MARQUARDT, R, BIRR, E, WOHLLEBEN, W, AUFDERHEIDE, K, PUÊHLER, A
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container_end_page 487
container_issue 4
container_start_page 481
container_title Applied microbiology and biotechnology
container_volume 34
creator BRAÊU, B
HILGENFELD, R
SCHLINGMANN, M
MARQUARDT, R
BIRR, E
WOHLLEBEN, W
AUFDERHEIDE, K
PUÊHLER, A
description Streptomyces coelicolor "Müller" DSM3030 excretes a lysozyme comprising both beta-1,4-N-acetyl- and beta-1,4-N,6-O-diacetyl muramidase activities. The lysozyme is named Cellosyl. Gene libraries have been established using genomic DNA from the wild-type strain, S. coelicolor DSM3030, and from an overproducing mutant, S. coelicolor HP1, which exhibits about a twofold increase in lysozyme production. The lysozyme-encoding genes (cel) from both strains were detected by oligodeoxynucleotide hybridization. The nucleotide sequence of the cel genes isolated from both strains was shown to be identical. The different levels of lysozyme production could not be correlated with any mutations at the cel gene locus. The cel gene isolated from the wild-type strain could not be expressed in some other species of Streptomyces. However, self-cloning of the cel gene into S. coelicolor DSM3030 and HP1 resulted in a 2.5-fold increase in lysozyme production.
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The lysozyme is named Cellosyl. Gene libraries have been established using genomic DNA from the wild-type strain, S. coelicolor DSM3030, and from an overproducing mutant, S. coelicolor HP1, which exhibits about a twofold increase in lysozyme production. The lysozyme-encoding genes (cel) from both strains were detected by oligodeoxynucleotide hybridization. The nucleotide sequence of the cel genes isolated from both strains was shown to be identical. The different levels of lysozyme production could not be correlated with any mutations at the cel gene locus. The cel gene isolated from the wild-type strain could not be expressed in some other species of Streptomyces. However, self-cloning of the cel gene into S. coelicolor DSM3030 and HP1 resulted in a 2.5-fold increase in lysozyme production.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>1367230</pmid><doi>10.1007/BF00180575</doi><tpages>7</tpages></addata></record>
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subjects Amino Acid Sequence
Base Sequence
Biological and medical sciences
Biotechnology
Cloning, Molecular
DNA, Bacterial - chemistry
Fundamental and applied biological sciences. Psychology
Genes, Bacterial
Genetic engineering
Genetic technics
Genomic Library
Methods. Procedures. Technologies
Molecular cloning
Molecular Sequence Data
Muramidase - biosynthesis
Muramidase - genetics
Restriction Mapping
Streptomyces - enzymology
Streptomyces - genetics
title Increased yield of a lysozyme after self-cloning of the gene in Streptomyces coelicolor Müller
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