首页> 外文期刊>Journal of Cereal Science >Effect of the use of dilute alkaline prior to Bacillus subtilis-based biocontrol steeping and germination conditions on red sorghum malt beta-glucanase activities and residual beta-glucans.
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Effect of the use of dilute alkaline prior to Bacillus subtilis-based biocontrol steeping and germination conditions on red sorghum malt beta-glucanase activities and residual beta-glucans.

机译:在基于枯草芽孢杆菌的生物防治浸泡和萌发条件之前使用稀碱对红色高粱麦芽β-葡聚糖酶活性和残留β-葡聚糖的影响。

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摘要

Malting is the ideal stage to deal with beta-glucans. Their hydrolysis is very important as the diffusion of both hormones and hydrolytic enzymes in the endosperm of germinated grain depend on it. A high malt beta-glucanase activity is not a guarantee of an extensive hydrolysis of beta-glucans. When Bacillus subtilis is used to control mould growth, red sorghum malt beta-glucanase activity (measured using carboxymethylcellulose as the substrate) was improved without significantly affecting the hydrolysis of malt beta-glucans. Thus, in order to reduce the residual beta-glucans content, soaking in 0.2% NaOH was combined with a biocontrol. Soaking in 0.2% NaOH is recognized as capable of improving grain hydration by opening-up the endosperm cell walls. The combined use of 0.2% NaOH with B. subtilis-based biocontrol treatments during red sorghum malting, leads to malt with increased beta-glucanase activity and a significant reduction of residual beta-glucans when compared with the 16 h biocontrol steeping without prior steeping in 0.2% NaOH. beta-glucanase activity increases with increased germination temperature and time while, conversely, the residual beta-glucans content of the malts decreases. Indeed, while the level of beta-glucanase was not vastly different between the malts obtained after steeping in distilled water and those obtained after 8 h steeping in 0.2% NaOH followed by 8 h resteeping in distilled water (NaOH + H2O treatment), their residual beta-glucans levels differ significantly. B. subtilis-based treatment leads to malt with improved beta-(1-3)- and beta-(1-4)-glucanase activities without significantly improved malt beta-(1-3),(1-4)-glucanase activity. While malts obtained after 84 h germination weren't significantly different in terms of malt beta-(1-3),(1-4)-glucanase activities for all steeping treatments, the use of 0.2% NaOH steeping prior to resteeping led to malts with improved beta-glucans content. Combining the steeping in dilute alkaline and biocontrol enables taking advantage of the dilute alkaline effect on residual beta-glucans content, due probably to the opening-up of the cell walls and the improvement of water uptake, and that of the biocontrol (improvement of beta-glucanase synthesis).
机译:麦芽制造是应对β-葡聚糖的理想阶段。它们的水解非常重要,因为发芽谷物的胚乳中激素和水解酶的扩散都依赖于它。高麦芽β-葡聚糖酶活性不能保证β-葡聚糖的广泛水解。当枯草芽孢杆菌用于控制霉菌生长时,红色高粱麦芽β-葡聚糖酶活性(以羧甲基纤维素为底物测得)得到改善,而不会显着影响麦芽β-葡聚糖的水解。因此,为了减少残留的β-葡聚糖含量,将浸泡在0.2%NaOH中的溶液与生物防治剂混合使用。浸泡在0.2%NaOH中被认为能够通过打开胚乳细胞壁来改善谷物的水合作用。与未经事先浸泡的16 h生物防治浸泡相比,将0.2%NaOH与枯草芽孢杆菌的生物防治方法结合使用可导致麦芽的β-葡聚糖酶活性增强,且残留的β-葡聚糖显着减少。 0.2%NaOH。 β-葡聚糖酶活性随着发芽温度和时间的增加而增加,相反,麦芽中残留的β-葡聚糖含量降低。实际上,虽然浸入蒸馏水后的麦芽与浸入0.2%NaOH 8小时后再浸入蒸馏水(NaOH + H 2 <8 h)中获得的麦芽之间,β-葡聚糖酶的水平没有太大差异。 / sub> O处理),其残留的β-葡聚糖水平明显不同。基于枯草芽孢杆菌的处理方法导致麦芽的β-(1-3)-和β-(1-4)-葡聚糖酶活性得到改善,而麦芽β-(1-3),(1-4)-葡聚糖酶活性却没有得到明显改善。 。尽管所有浸泡处理的麦芽β-(1-3),(1-4)-葡聚糖酶活性在发芽84小时后获得的麦芽没有显着差异,但在重新浸泡前使用0.2%NaOH浸泡会导致麦芽改善了β-葡聚糖的含量。将稀碱浸泡与生物防治相结合,可以利用稀碱性对残留β-葡聚糖含量的影响,这可能是由于细胞壁的开放和水吸收的改善以及生物防治(β的改善) -葡聚糖酶合成)。

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