4.7 Article

Biochemical and molecular characterization of a thermostable chitosanase produced by the strain Paenibacillus sp 1794 newly isolated from compost

期刊

APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
卷 97, 期 13, 页码 5801-5813

出版社

SPRINGER
DOI: 10.1007/s00253-012-4483-4

关键词

Chitosan; Chitosanase; Oligosaccharide; Thermostability; Cleavage pattern; Paenibacillus

资金

  1. Natural Science and Engineering Council of Canada
  2. Arbeitsgemeinschaft industrieller Forschungsvereinigungen, Koln, Germany [16203N]

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Chitosan raises a great interest among biotechnologists due to its potential for applications in biomedical or environmental fields. Enzymatic hydrolysis of chitosan is a recognized method allowing control of its molecular size, making possible its optimization for a given application. During the industrial hydrolysis process of chitosan, viscosity is a major problem; which can be circumvented by raising the temperature of the chitosan solution. A thermostable chitosanase is compatible with enzymatic hydrolysis at higher temperatures thus allowing chitosan to be dissolved at higher concentrations. Following an extensive micro-plate screening of microbial isolates from various batches of shrimp shells compost, the strain 1794 was characterized and shown to produce a thermostable chitosanase. The isolate was identified as a novel member of the genus Paenibacillus, based on partial 16S rDNA and rpoB gene sequences. Using the chitosanase (Csn1794) produced by this strain, a linear time course of chitosan hydrolysis has been observed for at least 6 h at 70 degrees C. Csn1794 was purified and its molecular weight was estimated at 40 kDa by SDS-PAGE. Optimum pH was about 4.8, the apparent K-m and the catalytic constant k(cat) were 0.042 mg/ml and 7,588 min(-1), respectively. The half-life of Csn1794 at 70 degrees C in the presence of chitosan substrate was > 20 h. The activity of chitosanase 1794 varied little with the degree of N-acetylation of chitosan. The enzyme also hydrolyzed carboxymethylcellulose but not chitin. Chitosan or cellulose-derived hexasaccharides were cleaved preferentially in a symmetrical way (3+3) but hydrolysis rate was much faster for (GlcN)(6) than (Glc)(6). Gene cloning and sequencing revealed that Csn1794 belongs to family 8 of glycoside hydrolases. The enzyme should be useful in biotechnological applications of chitosan hydrolysis, dealing with concentrated chitosan solutions at high temperatures.

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