首页> 外文期刊>Preparative biochemistry & biotechnology: An international journal for rapid communication >COST-EFFECTIVE ENDO-MANNANASE FROM Bacillus sp. CFR1601 AND ITS APPLICATION IN GENERATION OF OLIGOSACCHARIDES FROM GUAR GUM AND AS DETERGENT ADDITIVE
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COST-EFFECTIVE ENDO-MANNANASE FROM Bacillus sp. CFR1601 AND ITS APPLICATION IN GENERATION OF OLIGOSACCHARIDES FROM GUAR GUM AND AS DETERGENT ADDITIVE

机译:芽孢杆菌成本有效的内切甘露聚糖酶。 CFR1601及其在瓜尔胶中低聚糖的生产及作为添加剂的应用

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摘要

The indigenous bacteria Bacillus sp. CFR1601 produced significant levels of endomannanase when grown on agro-wastes, namely, green gram husk and sunflower oil cake (25.6 IU=mL), used as sole carbon and nitrogen sources, respectively. Under immobilized cell system, synthetic supports (polyurethane foam, scotch brite, polyester; up to 33.2 IU=mL) were found marginally superior as compared to natural supports (cotton and silk; up to 28.2 IU=mL) for endo-mannanase production. Cooperative interactions between L-lysine HCl (0.3% w=v), Tween 60 (0.3% v=v), and sunflower oil cake (3.0% w=v) in central composite design response surface methodology ameliorated (1.61-fold) endo-mannanase titers to 48.0 IU=mL. Partially purified endo-mannanase was tested for its ability to produce oligosaccharides from guar gum. These oligosaccharides were tested in vitro for their ability to promote growth of Lactobacillus plantarum MTCC 5422 and Lactobacillus salivarius CHS 1E. Results indicated that low-molecular-weight degraded products from guar gum were (1) able to support the growth of tested strains [increased O.D_(600nm) up to 2.3-fold and decrease in pH (<6.3) due to production of short chain fatty acid (SCFA)] when used as sole carbon source; and (2) after purification and analysis by electron spray ionization–mass spectrometry (ESI-MS) were found to be composed of mainly disaccharide and tetrasaccharide. The compatibility of endo-mannanase with various detergents together with wash performance test confirmed its potential applicability for laundry industry.
机译:本土细菌芽孢杆菌。当在农业废料上生长时,CFR1601产生显着水平的甘露聚糖酶,即分别用作唯一碳源和氮源的绿色豆皮和葵花籽油饼(25.6 IU = mL)。在固定化细胞系统下,发现内切甘露聚糖酶的合成支持物(聚氨酯泡沫,苏格兰威士忌,聚酯;最高33.2 IU = mL)比天然支持物(棉和丝;最高28.2 IU = mL)略胜一筹。在中心复合设计响应表面方法中,L-赖氨酸HCl(0.3%w = v),Tween 60(0.3%v = v)和葵花籽油饼(3.0%w = v)之间的协同相互作用改善了(1.61倍)内-甘露聚糖酶滴度至48.0 IU = mL。测试了部分纯化的内甘露聚糖酶从瓜耳胶中产生寡糖的能力。在体外测试了这些寡糖促进植物乳杆菌MTCC 5422和唾液乳杆菌CHS 1E生长的能力。结果表明,瓜尔豆胶的低分子量降解产物(1)能够支持被测菌株的生长[OD_(600nm)增加至2.3倍,pH值的降低(<6.3)由于产生了瓜耳胶。短链脂肪酸(SCFA)]用作唯一碳源时; (2)经过电子喷雾电离质谱(ESI-MS)纯化和分析后,发现主要由二糖和四糖组成。甘露聚糖内切酶与各种洗涤剂的相容性以及洗涤性能测试证实了其在洗衣业中的潜在适用性。

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