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Isolation and Screening of Fungal Isolates from Bambara (Vigna Subterranea) Nuts for Tannase Production

机译:班巴拉(Vigna地下)坚果中单宁酶生产的真菌分离物的分离和筛选

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摘要

Tannase (Tannin acyl hydrolase, EC 3.1.1.20) is an enzyme produced in the presence of tannic acid by various filamentous fungi. They are produced principally by fungi of the genus Aspergillus and Penicillium. The enzyme is used in the food and beverage industry as a clarifying agent for wines, beers and fruit juices. In Africa, billions of dollars are expended yearly on the importation of commercial enzymes for the food and pharmaceutical industries and this increases the cost of production and the finished goods. This study was carried out to isolate tannase producing fungal species using Bambara nuts as a substrate in a bid to finding alternatives to the importation of tannase. Fresh Bambara nuts were collected from different locations in Nigeria. They were cleaned, sorted and intermittently moistened with water to encourage fungal growth for fourteen days. The different fungi obtained after fourteen days were inoculated onto Potato Dextrose Agar plates and incubated at 25°C for five days. Subculturing of fungal isolates was carried out to obtain pure cultures of isolates. Tannilytic activity (hydrolysis of tannin) of isolates was assessed by inoculating them in media containing tannin. The plates were incubated at 25°C for 2-5 days after which the plates were observed and zones of hydrolysis measured. A total of eighteen isolates were obtained. They were all members of the Aspergillus genus. 56% (10) of the isolates were able to degrade tannin acid with mean zone of hydrolysis of 39mm ±23.7 mm (Range 10-70mm). This study established members of the Aspergillus genus isolated from Bambara nuts as viable fungi for application in the production of tannase. This study adds to existing reports on fungal production of tannase.
机译:单宁酶(单宁酰基水解酶,EC 3.1.1.20)是在单宁酸存在下由各种丝状真菌产生的酶。它们主要由曲霉属和青霉属的真菌产生。该酶在食品和饮料工业中用作葡萄酒,啤酒和果汁的澄清剂。在非洲,每年花费数十亿美元用于食品和制药行业的商业酶的进口,这增加了生产和制成品的成本。这项研究是使用班巴拉坚果作为底物来分离产生鞣酸酶的真菌种类的,目的是寻找替代鞣酸酶进口的方法。新鲜的班巴拉坚果是从尼日利亚的不同地方收集的。将它们清洗,分类并用水间歇性润湿,以鼓励真菌生长十四天。 14天后获得的不同真菌被接种到马铃薯葡萄糖琼脂平板上,并在25℃下孵育5天。进行真菌分离物的传代培养以获得分离物的纯培养物。通过将分离物接种在含单宁的培养基中来评估其分离物的鞣制活性(单宁水解)。将板在25℃温育2-5天,之后观察板并测量水解区域。总共获得十八个分离株。他们都是曲霉属的成员。 56%(10)的分离物能够降解单宁酸,平均水解区为39mm±23.7 mm(范围10-70mm)。这项研究确定了从班巴拉坚果中分离出的曲霉属成员,作为活菌用于鞣酸酶的生产。该研究增加了有关鞣酸酶真菌生产的现有报道。

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