4.7 Article

Adhesions of extracellular surface-layer associated proteins in Lactobacillus M5-L and Q8-L

Journal

JOURNAL OF DAIRY SCIENCE
Volume 99, Issue 2, Pages 1011-1018

Publisher

ELSEVIER SCIENCE INC
DOI: 10.3168/jds.2015-10020

Keywords

Lactobacillus; surface-layer associated proteins; adhesion; identification

Funding

  1. National Natural Science Foundation of China (Beijing) [31301515]
  2. China Postdoctoral Science Foundation (Beijing) [2012M510093, 2013T60382]
  3. Natural Science Foundation of Heilongjiang Province (Harbin, China) [C201433]
  4. Fundamental Research Funds for the Central Universities (Harbin, China) [HIT.NSRIF.2012082]

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Surface-layer associated proteins (SLAP) that envelop Lactobacillus paracasei ssp. paracasei M5-L and Lactobacillus casei Q8-L cell surfaces are involved in the adherence of these strain to the human intestinal cell line HT-29. To further elucidate some of the properties of these proteins, we assessed the yields and expressions of SLAP under different incubation conditions. An efficient and selective extraction of SLAP was obtained when cells of Lactobacillus were treated with 5 M LiCl at 37 degrees C in aerobic conditions. The SLAP of Lactobacillus M5-L and Q8-L in cell extracts were visualized by SDS-PAGE and identified by Western blotting with sulfo-N-hydroxysuccinimide-biotin labeled HT-29 cells as adhesion proteins. Atomic force microscopy contact imaging revealed that Lactobacillus strains M5-L and Q8-L normally display a smooth, homogeneous surface, whereas the surfaces of M5-L and Q8-L treated with 5 M LiCl were rough and more heterogeneous. Analysis of adhesion forces revealed that the initial adhesion forces of 1.41 and 1.28 nN obtained for normal Lactobacillus M5-L and Q8-L strains, respectively, decreased to 0.70 and 0.48 nN, respectively, following 5 M LiCl treatment. Finally, the dominant 45-kDa protein bands of Lactobacillus Q8-L and Lactobacillus M5-L were identified as elongation factor Tu and surface antigen, respectively, by liquid chromatography-tandem mass spectrometry.

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