安可,史晓翀,崔方元,等.噬琼胶卵链菌β-琼胶酶基因YM01-5的克隆表达及其酶学性质的研究[J].中国海洋药物,2018,37(1):31-39.
噬琼胶卵链菌β-琼胶酶基因YM01-5的克隆表达及其酶学性质的研究
Cloning, expression, and characterization of beta-agarase YM01-5 from Catenovulum agarivorans YM01T
投稿时间:2017-04-25  修订日期:2017-06-02
DOI:
中文关键词:  β-琼胶酶YM01-5  克隆表达  酶学性质  新琼二糖
English Keywords:beta-agarase YM01-5  Cloning and expression  characterization  neoagarobiose
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作者单位E-mail
安可 中国海洋大学 海洋生命学院 anke1228@qq.com 
史晓翀* 中国海洋大学 海洋生命学院 shixiaochong@ouc.edu.cn 
崔方元 中国海洋大学 海洋生命学院  
程景广 中国海洋大学 海洋生命学院  
刘娜 中国海洋大学 海洋生命学院  
张晓华 中国海洋大学 海洋生命学院  
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中文摘要:
      目的 从青岛近海海水中分离鉴定了1株能够降解琼胶的海洋新菌—嗜琼胶卵链菌(Catenovulumagarivoransgen. nov. sp. nov.)YM01T,并对其进行了全基因组测序。本文对该菌的1个β-琼胶酶基因YM01-5进行了克隆表达,并对重组琼胶酶的酶学性质进行了研究。方法 利用镍柱亲和层析对重组琼胶酶进行了分离纯化,采用DNS法测定重组酶的酶学性质,薄层层析(TLC)和质谱(MS)法对AgaYM01-5的酶解产物进行分析。结果 β-琼胶酶基因YM01-5全长2 412 bp,编码803个氨基酸,预测分子量为91.6 kDa,其催化模块属于糖苷水解酶GH50家族。重组琼胶酶YM01-5酶学性质的研究结果表明,该酶的最适温度为40 ℃,最适pH为9.0。在35 ℃以下具有良好的热稳定性,pH 6~10之间保持较高的稳定性,在该范围的pH缓冲液中放置12 h后,YM01-5仍能保持80%以上的酶活力。此外,该重组琼胶酶降解琼脂糖的Km、Vmax值分别为15.6 mg/mL和188 U/mg, 对降解产物的薄层层析及质谱分析结果表明,β-琼胶酶基因YM01-5以外切酶的形式作用于琼脂糖产生新琼二糖作为终产物。结论 该酶降解产物单一,有利于琼胶寡糖的制备,具有较高的工业应用潜力,它的发现也为研究菌株YM01中琼脂糖的代谢通路提供了参考。
English Summary:
      objective An agar-degrading bacterium, Catenovulum agarivorans YM01T, was isolated from the seawater of Qingdao, China and identified as a novel genus and species. The genome sequencing of this strain has already been completed. In this study, a new β-agarase gene YM01-5 was cloned and overexpressed in E.coli BL21 (DE3) system. Then the characterizations of the recombinantagaraseYM01-5 were analyzed. Methods The His-tagged recombinant proteins were purified using NTA-Ni2+agarose affinity chromatography from the crude extract. The characterizations of the recombinant agarase YM01-5 were analyzed by dinitro salicylic acid method. The hydrolysis products of AgaYM01-5 was analyzed by thin-layer chromatography (TLC) and mass spectrometry (MS). Results The gene agaYM01-5 consisted of 2,412 bp and encoded a protein of 803 amino acids with an apparent molecular mass of 91.6 kDa. YM01-5 belonged to glycoside hydrolase 50 family based on the amino acid sequence homology. The optimum pH and temperature of YM01-5 were 7.0 and 50 °C, respectively. It was stable at pH 6.0~10.0 and temperatures below 35 °C. It retained more than 80% activity after being preincubated at a wide range of pH 6.0~10.0 at 4 °C for 12 h. The Km and Vmax for agarose were 15.6 mg/mL and 188 U/mg,respectively. Thin layer chromatography (TLC) and ion trap mass spectrometer of the YM01-5 hydrolysis products displayed that YM01-5 was an exo-type β-agarase and degraded agarose into neoagarobiose directly. Conclusion The enzyme YM01-5 could digest agarose yielding neoagarobiose as the single end product, which had potential applications for the production of oligosaccharides with remarkable activities. While it also provided a better understanding of agarolytic metabolic pathway in YM01T.
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