Lactamase of Lysobacter enzymogenes: cloning, characterization and expression of the gene and comparison of the enzyme to other lactamases

التفاصيل البيبلوغرافية
العنوان: Lactamase of Lysobacter enzymogenes: cloning, characterization and expression of the gene and comparison of the enzyme to other lactamases
المؤلفون: Kenneth L. Roy, Richard G. Von Tigerstrom, Samson Au, Gregory J. Boras
المصدر: Journal of General Microbiology. 139:1245-1252
بيانات النشر: Microbiology Society, 1993.
سنة النشر: 1993
مصطلحات موضوعية: DNA, Bacterial, Molecular Sequence Data, EcoRI, Gene Expression, Sequence alignment, Molecular cloning, medicine.disease_cause, Microbiology, beta-Lactamases, medicine, Amino Acid Sequence, Cloning, Molecular, Escherichia coli, Peptide sequence, Gene, chemistry.chemical_classification, Bacteria, Base Sequence, Sequence Homology, Amino Acid, biology, Nucleic acid sequence, Molecular biology, Amino acid, chemistry, Biochemistry, Genes, Bacterial, biology.protein
الوصف: The gene for the periplasmic beta-lactamase of Lysobacter enzymogenes was isolated as part of a 1017 bp EcoRI fragment and the nucleotide sequence of the gene was determined. It has a G+C content of 71.5% and encodes a 27 amino acid signal sequence and the mature beta-lactamase of 276 amino acids which has a mass of 29,146 Da. The enzyme appears to be unique to L. enzymogenes but its amino acid sequence shows a high degree of homology with the amino acid sequences of the lactamase from Citrobacter diversus and other Class A beta-lactamases. The beta-lactamase gene of L. enzymogenes was expressed in Escherichia coli using pUC118 as the vector. The production of active beta-lactamase was highest after the active growth phase of the expression host and reached levels which were about three times higher than those obtained with L. enzymogenes.
تدمد: 0022-1287
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bd271149bc72ff3572dfb69fdd3154b
https://doi.org/10.1099/00221287-139-6-1245
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....8bd271149bc72ff3572dfb69fdd3154b
قاعدة البيانات: OpenAIRE