Influence of cooling temperature and duration on cold adaptation of Lactobacillus acidophilus RD758

Cryobiology. 2005 Jun;50(3):294-307. doi: 10.1016/j.cryobiol.2005.03.001. Epub 2005 Apr 18.

Abstract

The effect of different cooling temperatures and durations on resistance to freezing and to frozen storage at -20 degrees C in Lactobacillus acidophilus RD758 was studied, by using a central composite rotatable design. A cold adaptation was observed when the cells were maintained at moderate temperature (26 degrees C) for a long time (8h) before being cooled to the final temperature of 15 degrees C. These conditions led to a low rate of loss in acidification activity during frozen storage (0.64 minday(-1)) and a high residual acidification activity after 180 days of frozen storage (1011 min). The experimental design allowed us to determine optimal cooling conditions, which were established at 28 degrees C during 8h. Adaptation to cold temperatures was related to an increase in the unsaturated to saturated fatty acid ratio and in the relative cycC19:0 fatty acid concentration. Moreover, an increased synthesis of four specific proteins was observed as an adaptive response to the optimal cooling conditions. They included the stress protein ATP-dependent ClpP and two cold induced proteins: pyruvate kinase and a putative glycoprotein endopeptidase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acclimatization / physiology*
  • Animals
  • Bacterial Proteins / metabolism
  • Cell Membrane / chemistry
  • Cell Membrane / metabolism
  • Chromatography, Gas
  • Cold Temperature*
  • Cryopreservation*
  • Electrophoresis, Gel, Two-Dimensional
  • Endopeptidases / metabolism
  • Fatty Acids / analysis
  • Fatty Acids / metabolism
  • Lactobacillus acidophilus / physiology*
  • Proteome
  • Pyruvate Kinase / metabolism
  • Serine Endopeptidases / metabolism
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
  • Time Factors

Substances

  • Bacterial Proteins
  • Fatty Acids
  • Proteome
  • Pyruvate Kinase
  • Endopeptidases
  • ClpP2 protein, bacteria
  • Serine Endopeptidases