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一种新型厌氧瘤胃细菌内切/外切型纤维素酶。

A novel bifunctional endo-/exo-type cellulase from an anaerobic ruminal bacterium.

机构信息

Microbe-based Fusion Technology Research Center, KRIBB, 1404 Sinjeong-dong, Jeongeup, Jeonbuk 580-185, Republic of Korea.

出版信息

Appl Microbiol Biotechnol. 2011 Mar;89(5):1453-62. doi: 10.1007/s00253-010-2949-9. Epub 2010 Nov 3.

Abstract

An anaerobic microorganism termed AN-C16-KBRB was isolated from the bovine rumen and demonstrated cellulolytic activity on a NB agar plate containing azo-carboxymethyl cellulose. The 16S rRNA gene of the strain was 98% similar to that of Clostridiaceae bacterium SK082 (AB298754) as the highest homology. A novel celEdx16 gene encoding a bifunctional endo-/exocellulase (CelEdx16) was cloned by the shotgun method from AN-C16-KBRB, and the enzyme was characterized. The celEdx16 gene had an open reading frame of 1,104-base pairs, which encoded 367 amino acids to yield a protein of molecular mass 40.4 kDa. The amino acid sequence was 53% identical to that of an endoglucanase from Clostridium thermocellum. CelEdx16 was overexpressed in Escherichia coli and purified using Ni-NTA affinity chromatography. The specific endocellulase and exocellulase activities of CelEdx16 were 15.9 and 3.6 x 10⁻² U mg⁻¹, respectively. The Michaelis-Menten constant (K (m) values) and the maximal reaction velocities (V(max) values) of CelEdx16 were 47.1 μM and 9.6 x 10⁻³ μmole min⁻¹ when endocellulase activity was measured and 106.3 μM and 2.1 x 10⁻⁵ μmol min⁻¹ when exocellulase activity was assessed. CelEdx16 was optimally active at pH 5.0 and 40 °C.

摘要

从牛瘤胃中分离到一种称为 AN-C16-KBRB 的厌氧微生物,在含有偶氮羧甲基纤维素的 NB 琼脂平板上表现出纤维素酶活性。该菌株的 16S rRNA 基因与梭菌科 SK082 细菌(AB298754)的相似度最高,为 98%。通过鸟枪法从 AN-C16-KBRB 中克隆了一种新型 celEdx16 基因,该基因编码一种具有内切酶/外切酶活性的双功能酶(CelEdx16),并对该酶进行了表征。celEdx16 基因的开放阅读框长 1104 个碱基对,编码 367 个氨基酸,产生分子量为 40.4 kDa 的蛋白质。该氨基酸序列与来源于嗜热梭菌的内切葡聚糖酶有 53%的同源性。CelEdx16 在大肠杆菌中过表达,并使用 Ni-NTA 亲和层析进行纯化。CelEdx16 的内切酶和外切酶比活分别为 15.9 和 3.6×10⁻² U mg⁻¹。当测定内切酶活性时,CelEdx16 的米氏常数(K (m) 值)和最大反应速度(V(max) 值)分别为 47.1 μM 和 9.6×10⁻³ μmole min⁻¹,当测定外切酶活性时,分别为 106.3 μM 和 2.1×10⁻⁵ μmol min⁻¹。CelEdx16 的最适 pH 值和温度分别为 5.0 和 40°C。

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