期刊
MICROBIAL CELL FACTORIES
卷 20, 期 1, 页码 -出版社
BMC
DOI: 10.1186/s12934-021-01575-6
关键词
Eps cluster; Exopolysaccharides; Limosilactobacillus (Lactobacillus) fermentum; Probiotic; Prebiotic
资金
- Croatian Science Foundation [IP-2014-09-7009, IP-2019-04-2237]
- University of Zagreb, Croatia [000700007439]
- FEMS Research and Training [FEMS-GO-2017-004]
Lactobacillus fermentum D12 is a strain capable of producing exopolysaccharides (EPS) with potential health benefits. Its whole genome analysis revealed key genes related to EPS biosynthesis, leading to the secretion of multiple EPSs under different culture conditions. EPS positively influences the survival and adhesion of D12, especially under simulated gastrointestinal tract conditions.
Lactobacillus (Limosilactobacillus) fermentum D12 is an exopolysaccharide (EPS) producing strain whose genome contains a putative eps operon. Whole-genome analysis of D12 was performed to disclose the essential genes correlated with activation of precursor molecules, elongation and export of the polysaccharide chain, and regulation of EPS synthesis. These included the genes required for EPS biosynthesis such as epsA, B, C, D and E, also gt, wzx, and wzy and those involved in the activation of the precursor molecules galE, galT and galU. Both the biosynthesis and export mechanism of EPS were proposed based on functional annotation. When grown on MRS broth with an additional 2% w/v glucose, L. fermentum D12 secreted up to 200 mg/L of a mixture of EPSs, whose porous structure was visualized by scanning electron microscopy (SEM). Structural information obtained by (HNMR)-H-1 spectroscopy together with composition and linkage analyses, suggested the presence of at least two different EPSs, a branched heteropolysaccharide containing t-Glcp and 2,6-linked Galf, and glycogen. Since recent reports showed that polysaccharides facilitate the probiotic-host interactions, we at first sought to evaluate the functional potential of L. fermentum D12. Strain D12 survived simulated gastrointestinal tract (GIT) conditions, exhibited antibacterial activity against enteropathogenic bacteria, adhered to Caco-2 cells in vitro, and as such showed potential for in vivo functionality. The EPS crude extract positively influenced D12 strain capacity to survive during freeze-drying and to adhere to extracellular matrix (ECM) proteins but did not interfere Caco-2 and mucin adherence when added at concentrations of 0.2, 0.5, and 1.0 mg/mL. Since the viable bacterial count of free D12 cells was 3 logarithmic units lower after the exposure to simulated GIT conditions than the initial count, the bacterial cells had been loaded into alginate for viability improvement. Microspheres of D12 cells, which were previously analyzed at SEM, significantly influenced their survival during freeze-drying and in simulated GIT conditions. Furthermore, the addition of the prebiotic substrates mannitol and lactulose improved the viability of L. fermentum D12 in freeze-dried alginate microspheres during 1-year storage at 4 degrees C compared to the control.
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