Biomaterial Database

[Fragmentation of the lactose-protease plasmid in lactose-negative derivatives of Streptococcus lactis and S. lactis ssp. diacetylactis]. 1983

P Ramos, and M Novel, and M Lemosquet, and G Novel

DNA analysis showed the presence of plasmids in all 29 strains of mesophilic lactic streptococci. Their number ranged from 1 to 9 and their molecular weight extended from 1.8 to 45 megadaltons (Md). Comparison of the plasmid profiles from 9 strains of Streptococcus lactis, 3 strains of S. lactis ssp. diacetylactis and from their Lac-,Prt-variants was carried out. In most of the strains, a single plasmid of 27 to 45 Md carried both the lactose and protease (lac and prt) determinants. In Lac- variants, this composite plasmid may at times be lost; in most derivatives, this plasmid was fragmented into several smaller plasmids. Fragmentation resulted in the inactivation of lac genes and often of prt genes; sometimes prt genes remained intact in one of these new plasmids. Fragmentation of the plasmid may also take place without inactivation of these metabolic genes. Restriction analysis of the lactose-protease plasmid from 3 strains of S. lactis and from one Lac-variant confirmed the plasmid fragmentation phenomenon, and led to a proposal for physical mapping of the plasmid and preliminary localization of the lac-prt genes.

UI	MeSH Term	Description	Entries
D007786	Lactose Factors	Plasmids which determine the ability of a bacterium to ferment lactose.	Lac Factors,Factors, Lac,Factors, Lactose
D008970	Molecular Weight	The sum of the weight of all the atoms in a molecule.	Molecular Weights,Weight, Molecular,Weights, Molecular
D010447	Peptide Hydrolases	Hydrolases that specifically cleave the peptide bonds found in PROTEINS and PEPTIDES. Examples of sub-subclasses for this group include EXOPEPTIDASES and ENDOPEPTIDASES.	Peptidase,Peptidases,Peptide Hydrolase,Protease,Proteases,Proteinase,Proteinases,Proteolytic Enzyme,Proteolytic Enzymes,Esteroproteases,Enzyme, Proteolytic,Hydrolase, Peptide
D010957	Plasmids	Extrachromosomal, usually CIRCULAR DNA molecules that are self-replicating and transferable from one organism to another. They are found in a variety of bacterial, archaeal, fungal, algal, and plant species. They are used in GENETIC ENGINEERING as CLONING VECTORS.	Episomes,Episome,Plasmid
D004262	DNA Restriction Enzymes	Enzymes that are part of the restriction-modification systems. They catalyze the endonucleolytic cleavage of DNA sequences which lack the species-specific methylation pattern in the host cell's DNA. Cleavage yields random or specific double-stranded fragments with terminal 5'-phosphates. The function of restriction enzymes is to destroy any foreign DNA that invades the host cell. Most have been studied in bacterial systems, but a few have been found in eukaryotic organisms. They are also used as tools for the systematic dissection and mapping of chromosomes, in the determination of base sequences of DNAs, and have made it possible to splice and recombine genes from one organism into the genome of another. EC 3.21.1.	Restriction Endonucleases,DNA Restriction Enzyme,Restriction Endonuclease,Endonuclease, Restriction,Endonucleases, Restriction,Enzymes, DNA Restriction,Restriction Enzyme, DNA,Restriction Enzymes, DNA
D004269	DNA, Bacterial	Deoxyribonucleic acid that makes up the genetic material of bacteria.	Bacterial DNA
D005798	Genes, Bacterial	The functional hereditary units of BACTERIA.	Bacterial Gene,Bacterial Genes,Gene, Bacterial
D013294	Lactococcus lactis	A non-pathogenic species of LACTOCOCCUS found in DAIRY PRODUCTS and responsible for the souring of MILK and the production of LACTIC ACID.	Streptococcus lactis,Lactococcus lactis subsp. lactis