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来自EFB堆肥的ADI1产生的细胞外木聚糖果胶分解酶

Extracellular Xylanopectinolytic Enzymes by ADI1 from EFB's Compost.

作者信息

Nawawi Muhammad Hariadi, Mohamad Rosfarizan, Tahir Paridah Md, Saad Wan Zuhainis

机构信息

Faculty of Biotechnology and Biomolecular Sciences, Universiti Putra Malaysia (UPM), 43400 Serdang, Selangor, Malaysia.

Institute of Tropical Forestry and Forest Products, Universiti Putra Malaysia (UPM), 43400 Serdang, Selangor, Malaysia.

出版信息

Int Sch Res Notices. 2017 Apr 24;2017:7831954. doi: 10.1155/2017/7831954. eCollection 2017.

Abstract

Microbial xylanase and pectinase are two extremely valuable enzymes, which have captivated much attention. This can be seen from the increased demand for these enzymes by many industrial sectors. This study investigates the isolation and screening of extracellular xylanopectinolytic enzymes-producing bacteria in a submerged fermentation (SmF). Samples are collected from the compost of empty fruit bunch (EFB) at Biocompost Pilot Plant, located at Biorefinery Plant, Universiti Putra Malaysia. From the experiment, out of 20 isolates, 11 isolates show xylanase or/and pectinase activity, and only one isolate (EFB-11) shows the concurrent activities of xylanase and pectinase. These activities are selected for enzyme production under submerged fermentation (quantitative screening). At the 72nd hour of incubation, xylanase and pectinase show the highest production, which ranges about 42.33 U/mL and 62.17 U/mL (with low amount of cellulase present), supplemented with 2% (w/v) of rice bran as carbon source at incubation temperature level, which is 30°C. Meanwhile, the pH of media is shifted to 8.42, which indicates that EFB-11 isolate is alkalotolerant bacteria and identified as ADI1. This strain proves to have potential in agroindustrial bioconversion and has a promising ability to scale up to an industrial scale.

摘要

微生物木聚糖酶和果胶酶是两种极具价值的酶,备受关注。许多工业部门对这些酶的需求不断增加,由此可见一斑。本研究调查了在深层发酵(SmF)中产生胞外木聚糖果胶分解酶的细菌的分离和筛选。样本取自马来西亚博特拉大学生物精炼厂生物堆肥试验厂的空果串(EFB)堆肥。实验结果显示,在20株分离菌株中,有11株表现出木聚糖酶或/和果胶酶活性,只有一株分离菌株(EFB-11)同时表现出木聚糖酶和果胶酶活性。这些活性被选用于深层发酵下的酶生产(定量筛选)。在培养72小时时,木聚糖酶和果胶酶产量最高,分别约为42.33 U/mL和62.17 U/mL(存在少量纤维素酶),在30°C的培养温度下,以2%(w/v)的米糠作为碳源。同时,培养基的pH值变为8.42,这表明EFB-11分离菌株是耐碱细菌,被鉴定为ADI1。该菌株在农业工业生物转化方面具有潜力,并且具有扩大到工业规模的良好能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c597/5421085/c815b7dfb18d/ISRN2017-7831954.001.jpg

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