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PMID: 9143115 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Induction of heat shock proteins DnaK, GroEL, and GroES by salt stress in Lactococcus lactis.

Applied and environmental microbiology ·Vol. 63 ·No. 5 ·1997-05-00 ·Pages 1826-37

Kilstrup M, Jacobsen S, Hammer K, Vogensen FK

Abstract

The bacterium Lactococcus lactis has become a model organism in studies of growth physiology and membrane transport, as a result of its simple fermentative metabolism. It is also used as a model for studying the importance of specific genes and functions during life in excess nutrients, by comparison of prototrophic wild-type strains and auxotrophic domesticated (dairy) strains. In a study of the capacity of domesticated strains to perform directed responses toward various stress conditions, we have analyzed the heat and salt stress response in the established L. lactis subsp. cremoris laboratory strain MG1363, which was originally derived from a dairy strain. After two-dimensional separation of proteins, the DnaK, GroEL, and GroES heat shock proteins, the HrcA (Orf1) heat shock repressor, and the glycolytic enzymes pyruvate kinase, glyceral-dehyde-3-phosphate dehydrogenase, and phosphoglycerate kinase were identified by a combination of Western blotting and direct N-terminal amino acid sequencing of proteins from the gels. Of 400 to 500 visible proteins, 17 were induced more than twofold during heat stress. Two classes of heat stress proteins were identified from their temporal induction pattern. The fast-induced proteins (including DnaK) showed an abruptly increased rate of synthesis during the first 10 min, declining to intermediate levels after 15 min. GroEL and GroES, which also belong to this group, maintained a high rate of synthesis after 15 min. The class of slowly induced proteins exhibited a gradual increase in the rate of synthesis after the onset of stress. Unlike other organisms, all salt stress-induced proteins in L. lactis were also subjected to heat stress induction. DnaK, GroEL, and GroES showed similar temporal patterns of induction during salt stress, resembling the timing during heat stress although at a lower induction level. These data indicate an overlap between the heat shock and salt stress responses in L. lactis.

MeSH Terms
Amino Acid Sequence Bacterial Proteins/analysis,immunology Blotting, Western Chaperonin 10/analysis,biosynthesis,immunology Chaperonin 60/analysis,biosynthesis,immunology DNA-Binding Proteins Electrophoresis, Gel, Two-Dimensional Escherichia coli Proteins Glyceraldehyde-3-Phosphate Dehydrogenases/analysis,immunology,metabolism HSP70 Heat-Shock Proteins/analysis,biosynthesis,immunology Heat-Shock Response Lactococcus lactis/metabolism,physiology Molecular Sequence Data Phosphoglycerate Kinase/analysis,immunology,metabolism Pyruvate Kinase/analysis,immunology,metabolism Repressor Proteins/analysis,biosynthesis,immunology Salts/pharmacology Sequence Analysis
Chemicals
Bacterial Proteins Chaperonin 10 Chaperonin 60 DNA-Binding Proteins Escherichia coli Proteins HSP70 Heat-Shock Proteins Repressor Proteins Salts Glyceraldehyde-3-Phosphate Dehydrogenases Pyruvate Kinase Phosphoglycerate Kinase dnaK protein, E coli
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Kilstrup M
Department of Microbiology, Technical University of Denmark, Lyngby, Denmark. mk@im.dtu.dk
Jacobsen S
Hammer K
Vogensen F K
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Article Info
Journal
Applied and environmental microbiology
Abbr.
Appl Environ Microbiol
ISSN
0099-2240
Published
1997-05-00
Pages
1826-37
Language
English
Region
United States
NLM ID
7605801
PMCID
PMC168475
Subset
IM
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