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Optimization of cultural conditions for tannase production by Pseudomonas aeruginosa IIIB 8914 under submerged fermentation

机译:发酵条件下铜绿假单胞菌IIIB 8914生产鞣酸酶的培养条件的优化

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摘要

A tannase yielding bacterial strain was isolated from soil sample collected from the area situated nearby small-scale tannery. It was identified as Pseudomonas aeruginosa IIIB 8914. The bacterial strain produced extra-cellular tannase under sub-merged fermentation (Smf) using amla (Phyllanthus emblica), keekar (Acacia nilotica), jamoa (Eugenia cuspidate) and jamun (Syzygium cumini) leaves. Among different substrates, amla and keekar leaves resulted in maximal extra-cellular production of tannase. Various process parameters were studied to optimize the extra-cellular yield of tannase under Smf. Maximum yield of tannase i.e., 13.65 and 12.90 U/ml was obtained when Smf was carried out using amla and keekar leaves (2% w/v) respectively in minimal media supplemented with MgSOp"7HO (amla)/HgCl (keekar), NHNO and 0.2% Tween 80; inoculated with 2% cell suspension, and incubated at 37pC for 24 h. The bacterial strain produced about 2 times (13.65 U/ml) higher yield of tannase than the highest reported yield of tannase (6 U/ml). Our finding suggests that agro residues in the form of amla and keekar leaves can be one of the best and cost effective alternatives to the costly pure tannic acid for industrial production of microbial tannase.
机译:从附近小型制革厂附近地区收集的土壤样品中分离出一种单宁酶产菌菌株。它被鉴定为铜绿假单胞菌IIIB8914。该细菌菌株在深层发酵(Smf)下使用amla(余甘子Phyllanthus emblica),keekar(Acacia nilotica),jamoa(Eugenia cuspidate)和jamun(Syzygium cumini)叶产生了胞外鞣酸酶。 。在不同的底物中,amla和keekar叶片导致鞣酸酶的最大细胞外产生。研究了各种工艺参数以优化Smf条件下鞣酸酶的细胞外产量。当分别在添加了MGp“ 7HO(amla)/ HgCl(keekar)和NHNO的基本培养基中分别使用amla和keekar叶片(2%w / v)进行Smf提取时,单宁酶的最大产量即13.65和12.90 U / ml。和0.2%Tween 80;接种2%细胞悬液,并在37pC下孵育24小时,细菌菌株产生的鞣酸酶产率比报道的最高鞣酸酶产率(6 U / ml)高约2倍(13.65 U / ml)。 )。我们的发现表明,以amla和keekar叶片形式存在的农业残留物可能是工业上生产鞣酸酶的成本高昂的纯单宁酸的最佳,最具成本效益的替代品之一。

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