Response of Lactobacillus helveticus PR4 to Heat Stress during Propagation in Cheese Whey with a Gradient of Decreasing Temperatures
Open accessAbstract
The heat stress response was studied in Lactobacillus helveticus PR4 during propagation in cheese whey with a gradient of naturally decreasing temperature (55 to 20°C). Growth under a gradient of decreasing temperature was compared to growth at a constant temperature of 42°C. Proteinase, peptidase, and acidification activities of L. helveticus PR4 were found to be higher in cells harvested when 40°C was reached by a gradient of decreasing temperature than in cells grown at constant temperature of 42°C. When cells grown under a temperature gradient were harvested after an initial exposure of 35 min to 55°C followed by decreases in temperature to 40 (3 h), 30 (5 h 30 min), or 20°C (13 h 30 min) and were then compared with cells grown for the same time at a constant temperature of 42°C, a frequently transient induction of the levels of expression of 48 proteins was found by two-dimensional electrophoresis analysis. Expression of most of these proteins increased following cooling from 55 to 40°C (3 h). Sixteen of these proteins were subjected to N-terminal and matrix-assisted laser desorption ionization-time of flight mass spectrometry analyses. They were identified as stress proteins (e.g., DnaK and GroEL), glycolysis-related machinery (e.g., enolase and glyceraldehyde-3-phosphate dehydrogenase), and other regulatory proteins or factors (e.g., DNA-binding protein II and ATP-dependent protease). Most of these proteins have been found to play a role in the mechanisms of heat stress adaptation in other bacteria.
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Some strains of L. helveticus such as CP790, CP53, and PR4 are able to hydrolyze both αs1- and β-casein.
“Some strains of L. helveticus such as CP790 (Yamamoto et al., 1994), CP53 (Ono et al., 1997), and PR4 (Di Cagno et al., 2006) are able to hydrolyze both αs1- and β-casein.”
From Lactobacillus helveticus: the proteolytic system (2013) · cites this paper as Di Cagno et al., 2006
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References 52 · Cited by 55
- Authors
- Di Cagno, R., De Angelis, M., Limitone, A., Fox, P. F., & Gobbetti, M.
- Affiliations
- Dipartimento di Protezione delle Piante e Microbiologia Applicata, Università degli Studi di Bari, Bari, Italy
- University of Bari Aldo Moro (IT)
- University College Cork (IE)
- ORCID
- Gobbetti, Marco
- Venue
- Applied and Environmental Microbiology
- Publisher
- American Society for Microbiology
- Published
- 2006-07
- Volume
- 72
- Issue
- 7
- Pages
- 4503-4514
- ISSN
- 0099-2240 (ISSN-L)
- 1098-5336
- OpenAlex
- W2123130325
- Cited by
- 55
- References
- 52
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 2 · 2022: 2 · 2021: 8 · 2020: 3 · 2019: 2 · 2018: 1 · 2017: 1 · 2016: 2 · 2014: 4 · 2013: 8 · 2012: 5
- FWCI
- 4.30
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Applied and Environmental Microbiology (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed (publishedVersion)
- CINECA IRIS Institutional Research Information System (University of Bari Aldo Moro) (submittedVersion)
- Open Research (University of Surrey) (submittedVersion)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Food Science › Probiotics and Fermented Foods
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Heat shock proteins research
- Keywords
- heat stress response, temperature gradient, whey, proteome, stress proteins, DnaK, GroEL, enolase, glyceraldehyde-3-phosphate dehydrogenase, ATP-dependent protease, protein expression, acidification activity, proteolytic activity, heat adaptation
- MeSH terms
- Amino Acid Sequence, Bacterial Proteins, Cheese, Hot Temperature, Kinetics, Molecular Sequence Data, Temperature, Electrophoresis, Gel, Two-Dimensional, Gene Expression Regulation, Bacterial, Heat-Shock Response, Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization, Lactobacillus helveticus
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