Journal of Agricultural Science and Technology ›› 2019, Vol. 21 ›› Issue (12): 49-57.DOI: 10.13304/j.nykjdb.2019.0357

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Gene Cloning and Characterization of a Novel Glucose Oxidase From Cladosporium tianshanense SL19

GE Jianzhong1, YIN Yaxin2, JIANG Xiao1, LIU Weina1, YAO Bin1, LUO Huiying1*   

  1. 1.Key Laboratory for Feed Biotechnology of the Ministry of Agriculture, Feed Research Institute, Chinese Academy of Agricultural Sciences, Beijing 100081, China; 2.College of Food Science and Engineering, Northwest A&F University, Yangling 712100, China
  • Received:2019-05-05 Online:2019-12-15 Published:2019-08-15

Cladosporium tianshanense SL19来源的新型葡萄糖氧化酶的基因克隆及性质研究

葛建忠1,尹亚昕2,蒋肖1,刘伟娜1,姚斌1,罗会颖1*   

  1. 1.中国农业科学院饲料研究所农业部饲料生物技术重点实验室, 北京100081; 2.中国陕西省杨凌区西北农林科技大学食品科学与工程学院, 陕西 杨凌 712100
  • 通讯作者: *通信作者 罗会颖 E-mail: luohuiying@caas.cn
  • 作者简介:葛建忠 E-mail: gejianzhong163@163.com;
  • 基金资助:
    现代农业产业技术体系项目(CARS-41)。

Abstract: Glucose oxidase (GOX) is widely used in various industrial processes. Few new types of GOX have been reported except from Aspergillus and Penicillium. A novel glucose oxidase gene CtgoxB from Cladosporium tianshanense SL19 was obtained by gene cloning and sequence homology analysis. The full-length DNA fragment of CtgoxB was 1 707 bp without intron, which encoded a protein of 568 amino acids with a signal peptide at N-terminal 1~16 amino acid residues. The amino acids sequence encoded by CtgoxB shared the highest identity of 35% with reported GOXs. The activity could not be detected when CtgoxB gene was expressed in P. pastoris. The mutant CtGOXB-C1 was obtained according to the sequence and structural analysis by homologous recombination, which recovered the activity of glucose oxidase. The molecular weight of recombinant CtGOXB-C1 showed about 120 kDa by SDS-PAGE, which was larger than the theoretical molecular weight (61.6 kDa). The purified recombinant glucose oxidase CtGOXB-C1 exhibited maximal activity at pH 8.0 and 30 ℃. Its specific activity was 123.8 U/mg, and it retained about 65% activity at 10 ℃ with a psychrophilic characteristic. The CtGOXB-C1 was stable at pH 6.0~9.0 and retained more than 80% of activity after incubating for 1 h, and maintained high enzyme activity under medium-alkaline condition and was highly resistant against SDS. All these favorable enzymatic properties showed that CtGOXB-C1 was a good candidate for the aquatic feeds and detergent industries.

Key words: glucose oxidase, Cladosporium tianshanense SL19, gene cloning, gene expression, characterization

摘要: 葡萄糖氧化酶(GOX)已广泛应用于各种工业生产中。目前,除了曲霉和青霉属来源的GOX外,鲜有新型GOX被报道。经基因克隆和序列同源性分析,Cladosporium tianshanense SL19来源的葡萄糖氧化酶基因CtgoxB是一个新基因,该基因全长1 707 bp,无内含子,编码568个氨基酸,N-端第1~16个氨基酸为信号肽,与已报道的GOX序列最高一致性为35%。CtgoxB在毕赤酵母中实现异源表达,但重组蛋白CtGOXB未检测到GOX活性。通过序列和结构分析,同源重组构建的突变体CtGOXB-C1最终恢复了GOX活性。经SDS-PAGE鉴定,重组蛋白CtGOXB-C1表观分子量约为120 kDa,大于理论分子量(61.6 kDa)。经酶学性质测定,CtGOXB-C1比活为123.8 U/mg,在pH 8.0和30 ℃条件下具有最高的酶活,且在10 ℃时依然维持65%的酶活,具有嗜低温特性。CtGOXB-C1在pH 6.0~9.0条件下保温1 h后,剩余酶活维持在80%以上,可以在中碱性条件下维持较高酶活,并且对表面活性剂SDS具有较强的抗性。这些性质表明CtGOXB-C1在水产饲料和洗涤剂等行业中具有良好的应用潜力。

关键词: 葡萄糖氧化酶, 枝孢菌SL19, 基因克隆, 基因表达, 性质研究