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Production of folate in oat bran fermentation by yeasts isolated from barley and diverse foods

机译:从大麦和多种食物中分离出的酵母在燕麦麸发酵中生产叶酸

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Aims: The focus of the research was to identify yeasts from barley kernels in order to study their folate production capability while maintaining high viscosity caused by soluble fibres in oat bran fermentation. Methods and Results: The 65 isolated yeasts were characterized by API carbohydrate utilization tests, and assays for extracellular enzyme activities were the following: amylase, beta-glucanase, cellulase or CMCase, lipase, protease and xylanase. Yeasts were identified by partial DNA sequencing of the 25S D1/D2 and ITS1-5.8S-ITS2 regions. They belonged to the genera Aureobasidium, Cryptococcus, Pseudozyma and Rhodotorula. Folate production was determined from supernatant and cells grown in a rich laboratory medium or directly from oat bran solution inoculated with the appropriate yeast. Food yeasts, Saccharomyces cerevisiae, Candida milleri, Kluyveromyces marxianus and Galactomyces geotrichum, were used for comparison. Most of the yeasts isolated from barley destroyed the solid, viscous structure of the oat bran solution, indicating that they degraded the viscosity-generating soluble fibres, considered to be nutritionally advantageous. The best folate producers were S. cerevisiae, followed by Pseudozyma sp., Rhodotorula glutinis and K. marxianus. The yeasts maintaining high viscosity were used together with lactic acid bacteria (LAB) Streptococcus thermophilus or Lactobacillus rhamnosus to ferment oat bran solution. None of the yeasts isolated from barley, contrary to S. cerevisiae and C. milleri, produced together with LAB significant amounts of folate. Conclusions: Fermentative yeasts together with LAB are potential for use in developing novel high folate content healthy foods and snacks from oat bran. Significance and Impact of the Study: High soluble fibre content and high natural folate content but low energy content food and snack products with pleasant fermentation aroma provide possibilities for new developments in the food industry
机译:目的:研究的重点是从大麦粒中鉴定酵母,以研究其叶酸生产能力,同时保持燕麦麸发酵中可溶性纤维引起的高粘度。方法和结果:通过API碳水化合物利用测试对65株分离的酵母进行了表征,细胞外酶活性的测定方法如下:淀粉酶,β-葡聚糖酶,纤维素酶或CMCase,脂肪酶,蛋白酶和木聚糖酶。通过对25S D1 / D2和ITS1-5.8S-ITS2区进行部分DNA测序来鉴定酵母。它们属于金黄色葡萄球菌属(Aureobasidium),隐球菌(Cryptococcus),假酶菌(Pseudozyma)和红假单胞菌(Rhodotorula)。由上清液和细胞在丰富的实验室培养基中或直接从接种了适当酵母的燕麦麸溶液中生长来确定叶酸的产生。使用食物酵母,酿酒酵母,假丝酵母​​,马克斯克鲁维酵母和土生半乳杆菌进行比较。从大麦中分离出的大多数酵母都破坏了燕麦麸溶液的固体粘性结构,表明它们降解了产生粘度的可溶性纤维,被认为具有营养优势。最好的叶酸生产者是酿酒酵母,其次是假酶菌,Rhodotorula glutinis和K. marxianus。保持高粘度的酵母与乳酸菌(LAB)嗜热链球菌或鼠李糖乳杆菌一起使用,以发酵燕麦麸皮溶液。与酿酒酵母和米氏酵母相反,从大麦中分离出的酵母中没有一个与LAB一起产生大量叶酸。结论:发酵酵母与LAB一起可用于开发燕麦麸中高叶酸含量的新型健康食品和零食。研究的意义和影响:高可溶性纤维含量和高天然叶酸含量,但低能量含量的食品和休闲食品以及令人愉悦的发酵香气为食品工业的新发展提供了可能性

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