Abstract

Sourdough fermentation is a common practice spread across the globe due to quality and shelf life improvement of baked goods. Above the widely studied exopolysaccharide (EPS) formation, which is exploited for structural improvements of foods including baked goods, β-glucan formation, by using lactic acid bacteria (LAB), offers additional values. Through renunciation of sucrose addition for bacterial β-d-glucan formation, which is required for the production of other homopolysaccharides, residual sweetness of baked goods can be avoided, and predicted prebiotic properties can be exploited. As promising starter cultures Levilactobacillus (L.) brevis TMW (Technische Mikrobiologie Weihenstephan) 1.2112 and Pediococcus (P.) claussenii TMW 2.340 produce O2-substituted (1,3)-β-d-glucan upon fermenting wheat and rye doughs. In this study, we have evaluated methods for bacterial β-glucan quantification, identified parameters influencing the β-glucan yield in fermented sourdoughs, and evaluated the sourdough breads by an untrained sensory panel. An immunological method for the specific detection of β-glucan proved to be suitable for its quantification, and changes in the fermentation temperature were related to higher β-glucan yields in sourdoughs. The sensory analysis resulted in an overall acceptance of the wheat and rye sourdough breads fermented by L. brevis and P. claussenii with a preference of the L. brevis fermented wheat sourdough bread and tart-flavored rye sourdough bread.

Highlights

  • Food fermentation by bacteria and yeasts is longer practiced than we know about the existence of microbes

  • EPSs produced by lactic acid bacteria (LAB) are either homopolysaccharides (HoPS) such as β- D -glucans, α- D glucans, and β-fructans, formed by the same monosaccharide units or heteropolysaccharides (HePS), which are mainly composed of D-glucose, D-galactose, and L-rhamnose

  • Changes in calculated β-glucan concentrations of the sourdoughs were almost identical between the same species strains with no significant differences between the wild-type strains, which are able to produce bacterial β-glucan and the ∆gtf-2 mutants

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Summary

Introduction

Food fermentation by bacteria and yeasts is longer practiced than we know about the existence of microbes. Β- D -glucans and HePS formation proceeds by intracellularly synthesis of nucleotide-activated sugar moieties and subsequent polymerization by glycosyltransferases (gtf ) [21,22,23,24,25]. By comparing both EPS types produced by LAB, extracellularly produced EPSs reach much higher yields (≤16 g/kg dough) than intracellular produced EPSs with yields below 0.6 g/L medium under optimal culture conditions [6,26]. It is previously reported that EPS formed by glucansucrase activity from sucrose during sourdough fermentation beneficially affects the viscoelastic properties, the texture, and shelf life of the dough [6]

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