Evaluation of exopolysaccharide producing Weissella cibaria MG1 strain for the production of sourdough from various flours
Introduction
A gluten-free diet is currently the only effective treatment for coeliac and gluten intolerant patients. Gluten-free breads often have a low nutritional value and are characterized by a low bread volume and a poor texture owing to the use of refined ingredients (pure starches and proteins), and the lack of the network forming gluten proteins (Gallagher et al., 2003). The use of nutrient-dense flours, for example, quinoa, buckwheat or teff, may improve the nutritional value (Hager et al., 2012) but does not provide a network forming protein. Hydrocolloids, such as xanthan, carrageen and agar, are used in bakery products as a replacement for gluten and to bind water in dough. Hydrocolloids also retard starch retrogradation, which is intimately linked to bread staling and shelf-life (Belitz et al., 2008). Microbial exopolysaccharides (EPS) are high molecular weight carbohydrate polymers found in some bacteria and microalgae (Monchois et al., 1999; van Hijum et al., 2006). Depending on their composition, they can be divided into homopolysaccharides (HoPS), consisting of one type of monosaccharide being either glucose (glucans) or fructose (fructans), and into heteropolysaccharides (made of 3–8 multiple, repeated moieties) (De Vuyst et al., 2001; van Hijum et al., 2006). In contrast to heteropolysaccharides which are synthesized in smaller amounts from sugar nucleotide precursors (De Vuyst et al., 2001), HoPS are synthesized in larger amounts from sucrose (Monsan et al., 2001).
HoPS-producing lactic acid bacteria are already used in conventional bread making (Decock and Cappelle, 2005, Lacaze et al., 2007), but their use is particularly promising in gluten-free baking (Galle et al., 2012, Ruehmkorf et al., 2012a, Ruehmkorf et al., 2012b, Schwab et al., 2008) since EPS can potentially act as hydrocolloids (Schwab et al., 2008). Microbial production of exopolysaccharides during sourdough fermentation was reported to be more effective than the addition of comparable amount of EPS to the bread formulation (Brandt et al., 2003).
Alternatively to EPS synthesis, sucrase-type enzymes catalyse the reactions sucrose hydrolysis and oligosaccharide formation (Tieking et al., 2003, van Hijum et al., 2006).
The production of oligosaccharides and polysaccharides by glucansucrases is dependent on the concentration and type of suitable acceptor carbohydrates (Galle et al., 2010, Kaditzky and Vogel, 2008, Tieking and Gänzle, 2005). Maltose is an efficient acceptor carbohydrate for dextransucrase present in cereals and diverts sucrose conversion from exopolysaccharide synthesis to oligosaccharide production (Galle et al., 2010, Kaditzky and Vogel, 2008). The concentration of maltose and other acceptor carbohydrates in sourdough depends on the carbohydrate composition as well as the enzyme activity of the cereal substrate thus influencing the yield of EPS and oligosaccharides in sourdough fermentations with EPS-producing starter cultures (Galle et al., 2010, Galle et al., 2012). The carbohydrate composition of wheat and rye flours as well as the evolution of carbohydrate levels in wheat and rye sourdoughs is well described (Roecken and Vosey, 1995). However, little data is available for other cereals or pseudocereals that are used in gluten-free baking.
During sucrose hydrolysis, fructose is released which can be used as an electron acceptor by most heterofermentative LAB and results in acetate formation (Gänzle et al., 2007). An excess of acetate compromises the quality of bread (Galle et al., 2010, Kaditzky and Vogel, 2008, Tieking and Gänzle, 2005). The obligate heterofermentative strain Weissella cibaria MG1 produced high amounts of the HoPS dextran (a α-1,6-linked glucan) from sucrose (Galle et al., 2010, Galle et al., 2012). Yet, comparable to other Weissella species, acetate formation was low, since W. cibaria MG1 lacks mannitol dehydrogenase activity and does not convert fructose to mannitol with concomitant acetate formation (Galle et al., 2010).
The strain-specific ability to produce exopolysaccharides during sourdough fermentation depends on the metabolic activity of the fermentation microbiota (Gänzle et al., 2007), and contributes to the sourdough's ability to influence bread quality (Galle et al., 2012, Katina et al., 2009).
It was the aim of this study to assess the production of EPS, oligosaccharides and organic acids by Weissella cibaria in sourdoughs. Protein degradation in gluten-free sourdoughs, as well as the effect of fermentation on dough rheology was also determined.
Section snippets
Materials
The ingredients used in this study were buckwheat flour (Doves Farm Foods Ltd, UK) (moisture 12.6%), oat flour (E. Flahavan & Son Ltd, Ireland, moisture 10.4%), quinoa flour (Ziegler Naturprodukte, Germany, moisture 12.3%), teff flour (Trouw, Netherlands, moisture 9.5%), wheat flour (baker's flour, Odlums, Ireland, moisture 12.7%) and sugar (Súicra, Ireland). All other chemicals and microbial media components were purchased from Sigma (Sigma, Arklow, Ireland), unless otherwise specified.
Strain and growth conditions
EPS and oligosaccharide production during sourdough fermentation
EPS were extracted from the flour, as well as from the 10% sucrose supplemented sourdough after completion of fermentation. The molecular weight of the EPS as analysed using SEC ranged between 106 and 107 Da (Fig. 1). Concentrations reached 0.9 g/kg dry weight sourdough in teff, 3.2 g/kg in quinoa and 4.2 g/kg in buckwheat. In wheat sourdough the amount of EPS did not exceed the initial amount of polysaccharides present in flour.
The qualitative analysis of oligosaccharides formed during
Discussion
The dextran forming strain W. cibaria MG1 grew well in buckwheat, teff and quinoa sourdoughs, in keeping with previous investigations (Galle et al., 2010; Moore et al., 2007). EPS were produced with a molecular weight of 5·106–4·107 Da in sucrose-supplemented sourdoughs, corroborating prior observations with the same strain in sorghum sourdough (Galle et al., 2010, Galle et al., 2011). The strain failed to grow during oat fermentations, likely due to the low concentration of fermentable sugars
Conclusion
Sourdough performance and yield of the exopolysaccharide dextran by W. cibaria depended on the substrate used and was highest in buckwheat and quinoa sourdough. The production of dextran was inversely related to oligosaccharide formation, and strongly depended on the concentration of the acceptor carbohydrate maltose. The presence of dextran positively influenced dough rheology imparting a softening effect in buckwheat and teff sourdoughs. Consequently, the heterofermentative lactic acid
Acknowledgements
The authors would like to thank Dan Walsh for excellent scientific and technical support. Furthermore, the authors' extend gratitude to Ann-Christin Reichel and Nicolò Gatti for their assistance. This study was financed by the Seventh framework Program of the European Community for research, technological development and demonstration activities (2007–2013); specific program “Capacities”- Research for the benefit of SMEs (262418 GLUTENFREE).
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2022, Carbohydrate PolymersCitation Excerpt :Accordingly, significance of Weissella strains to the technological characteristics of sourdough with respect to their EPS-producing properties were divulged by some investigations (Schwab et al., 2008; Wolter, Hager, Zannini, Czerny, & Arendt, 2014; Wolter, Hager, Zannini, Galle, et al., 2014). Importance of EPS production for Weissella strains was shown by several studies in which EPS produced by certain Weissella species from different media was characterized (Di Cagno et al., 2006; Schwab et al., 2008; Wolter, Hager, Zannini, Czerny, & Arendt, 2014; Wolter, Hager, Zannini, Galle, et al., 2014). Therefore, isolation of an EPS-producing LAB strain from sourdough media was the main purpose of this study.