Replication and temperature-sensitive maintenance functions of lactose plasmid pSK11L from Lactococcus lactis subsp. cremoris

• Published in: Journal of Bacteriology 1991-12, Vol.173 (23), p.7573-7581
• Main Authors: Horng, J.S. (University of Minnesota, St. Paul, MN), Polzin, K.M, McKay, L.L
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Bacteriology; Base Sequence; Biological and medical sciences; Blotting, Southern; CALOR; CHALEUR; Chromosome Deletion; DNA Replication; DNA, Bacterial - genetics; DNA, Bacterial - isolation & purification; Fundamental and applied biological sciences. Psychology; Genetics; Kinetics; Lactococcus lactis; Lactococcus lactis - genetics; Lactococcus lactis - physiology; LACTOSA; LACTOSE; Lactose - metabolism; Microbiology; Molecular Sequence Data; Mutagenesis, Insertional; NUCLEOTIDE; NUCLEOTIDOS; PLASMIDE; PLASMIDIOS; Plasmids; Replicon; RESISTANCE A LA TEMPERATURE; RESISTENCIA A LA TEMPERATURA; Restriction Mapping; STREPTOCOCCUS CREMORIS; STREPTOCOCCUS LACTIS; TEMPERATURA; TEMPERATURE
• ISSN: 0021-9193; 1098-5530; 1067-8832
• DOI: 10.1128/jb.173.23.7573-7581.1991

The replication region of pSK11L, the lactose plasmid of Lactococcus lactis subsp. cremoris (L. cremoris) SK 11, was isolated on a 14.8-kbp PvuII fragment by shotgun cloning into an Escherichia coli vector encoding erythromycin resistance and selection for erythromycin-resistant transformants of L. lactis subsp. lactis (L. lactis) LM0230. Deletion analysis and Tn5 mutagenesis of the resulting plasmid pKMP1) further localized the replication region to a 2.3-kbp ScaI-SpeI fragment. DNA sequence analysis of this 2.3-kbp fragment revealed a 1,155-bp open reading frame encoding the putative replication protein, Rep. The replication origin was located upstream of rep and consisted of an 11-bp imperfect direct repeat and a 22-bp sequence tandemly repeated three and one-half times. The overall organization of the pSK11L replicon was remarkably similar to that of pCI305, suggesting that pSK11L does not replicate by the rolling-circle mechanism. Like pSKIIL, pKMP1 was unstable in L. lactis LM0230. Deletion analysis allowed identification of several regions which appeared to contribute to the maintenance of pKMP1 in L. lactis LM0230. pKMP1 was significantly more stable in L. cremoris EB, than in L. lactis LM0230 at all of the temperatures compared. This stability was lost by deletion of a 3.1-kbp PvuII-Xbal fragment which had no effect on stability in L. lactis LM0230. Other regions affecting stability in L. cremoris EB5 but not in L. lactis LM0230 were also identified. Stability assays conducted at various temperatures showed that pKMP1 maintenance was temperature sensitive in both L. lactis LM0230 and L. cremoris EB5 although the plasmid was more unstable in L. lactis LM0230. The region responsible for the temperature sensitivity phenotype in L. lactis LM0230 was tentatively localized to a 1.2-kbp ClaI-HindIII fragment which was distinct from the replication region of pSK11L. Our results suggest that the closely related L. lactis and L. cremoris subspecies behave differently regarding maintenance of plasmids