Novel Protease-Resistant Exochitinase (Echi47) from Pig Fecal Environment DNA with Application Potentials in the Food and Feed Industries

作者：Liu, Yuchun; Yan, Qiaojuan; Yang, Shaoqing; Jiang, Zhengqiang^*

来源：Journal of Agricultural and Food Chemistry, 2015, 63(27): 6262-6270.

DOI：10.1021/acs.jafc.5b01457

• chitinase
• exochitinase
• metagenome
• direct cloning and heteroexpression
• N-acetylchitobiose
• protease resistance

A novel exochitinase gene (Echi47) was directly cloned from the pig fecal environment DNA using the genomic walking PCR technique and expressed in Escherichia coli BL21 (DE3). Echi47 has an open reading frame (ORE) of 1,161 bp encoding 386 amino acids. The amino acid sequence of Echi47 showed 36% identity with that of chitinase from Coprinellus congregatus. The recombinant exochitinase was purified with specific activity toward colloidal chitin of 6.84 U/mg. Echi47 was optimally active at pH 5.0 and 40 degrees C, respectively. When colloidal chitin was used as substrate, N-acetylthitobiose [(GlcNAc)(2)] was mostly produced at the initial stage, suggesting that it is an exochitinase. Echi47 exhibited excellent resistance to pepsin, trypsin, proteinase K, and flavor protease. Under simulated alimentary tract conditions, Echi47 was stable and active, releasing, 21.1 mg of N-acetylchitooligosactharides from 80 mg of colloidal chitin. These properties make Echi47 a potential additive in the food and feed industries.

• 出版日期2015-7-15
• 单位中国农业大学