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麻类脱胶高效菌株果胶裂解酶基因克隆与表达

Cloning and expression of a pectate lyase gene from an efficient strain for bast fiber bio-extracting
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摘要 【目的】克隆麻类脱胶高效菌株Dickeya sp.DCE-01的果胶裂解酶基因并进行原核表达,对表达产物进行纯化和酶学性质研究。【方法】根据该菌株全基因组序列预测的果胶裂解酶基因Q59419设计引物,PCR扩增后将该基因连接到pEASY-E1和pACYCDuet-1载体上,导入E.coli BL21(DE3)进行表达。选择酶活力高的阳性克隆子进行大量诱导表达后,采用超滤和Sephadex G-100凝胶层析两步法纯化出果胶裂解酶,研究其酶学性质。【结果】克隆到果胶裂解酶基因pel(GenBank登录号:JX964997),其序列全长1 128 bp,编码375个氨基酸。pACYCDuet-1-pel-BL表达胞外果胶裂解酶活力最高,发酵液粗酶活达298.8 IU/mL。其最适反应温度为50°C,最适pH为9.0;保温1 h,酶活稳定温度≤45°C,稳定pH为9.0?10.0。酶催化作用依赖于Ca2+,其最适作用浓度为2 mmol/L;Zn2+、Ca2+和NH4+促进酶活力,Fe3+和Pb2+严重抑制酶活力;聚半乳糖醛酸钠为该酶的最适底物。【结论】从麻类脱胶高效菌株中发掘到碱性果胶裂解酶基因,其表达产物在生物质加工过程中具有重要工业化应用前景。 [Objective] We cloned and expressed the pectate lyase gene (pel) from Dickeya sp. DCE-01, a strain for bast fiber bio-extracting, in E. coli BL21(DE3). Then we characterized the purified pectate lyase (Pel). ]Methods] Primers were designed by the potential pel Q59419 annotated from the whole genome sequence of Dickeya sp. DCE-01. The pel was cloned, linked to pEASY-E1 and pACYCDuet-1, and expressed in E. coli BL21(DE3). After comparing the activities of extracellular Pel from the engineering strains, the Pel with highest activity was purified by the two-step process involving ultrafiltration and gel filtration (Sephadex G-100) and then characterized. [Results] The pel (GenBank: JX964997) was 1 128 bp and encoded 375 amino acids. The highest activity of the extracellular Pel from pACY- CDuet-l-pel-BL strain was 298.8 IU/mL. The optimal condition for the purified enzyme was at 50 ℃, pH 9.0 and polygalacturonic acid sodium as a substrate. The catalytic activity of the purified Pel was stable below 45 ℃ for 1 h at pH 9.0-10.0. It was dependent on Ca&2+, while it was promoted by Zn^2+ and NH^4+ and inhibited seriously by Fe^3+ and Pb^2+. The maximal activ- ity of the purified enzyme was obtained at Ca&2+ concentration of 2 mmol/L. ]Conclusion] An efficient alkaline pectate lyase gene has been excavated from strain DCE-01, and its expres- sion product may be available for biorefinery.
出处 《微生物学通报》 CAS CSCD 北大核心 2013年第8期1403-1413,共11页 Microbiology China
基金 国家863计划项目(No.2006AA02Z249) 国家麻类产业技术体系建设专项项目(No.CARS-19-E24)
关键词 麻类脱胶 高效菌株 果胶裂解酶 基因克隆 酶学性质 Bast fiber bio-extracting Efficient strain Pectate lyase Gene clone Enzymatic prop-erty
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参考文献22

  • 1Gummadi SN, Kumar DS. Microbial pectic transelirninasesj'J]. Biotechnology Letters, 2005, 27(7): 451-458. 被引量:1
  • 2Pissavin C, Robert-Baudouy J, Hugouvieux?Cotte-Pattat N. Biochemical characterization of the pectate lyase PelZ of Erwiniachrysanthemi 3937[J]. Biochimica et BiophysicaActa, 1998, 1383(2): 188-196. 被引量:1
  • 3Reidl. Pectinase in papermaking: solving retention problems in mechanical pulps bleached with hydrogen peroxide[J]. Enzyme and Microbial Technology, 2000, 26(2/4): 115-123. 被引量:1
  • 4Ouattara HG, Reverchon S, Niamke SL, et al. Molecular identification and pectate lyase production by Bacillus strains involved in cocoa fermentation[J]. Food Microbiology, 20 II, 28(1): 1-8. 被引量:1
  • 5Tanabe H, Yoshihara K, Tamura K, et al. Pretreatment of pectic wastewater from orange canning process by an alkalophilic Bacillus sp.[J]. Journal of Fermentation Technology, 1987, 65(2): 243-246. 被引量:1
  • 6Xiao Z, Wang S, Bergeron H, et al. A flax-retting endopolygalacturonase-encoding gene from Rhizopus oryzaeU]. Antonie Van Leeuwenhoek, 2008,94(4): 563-571. 被引量:1
  • 7Basu S, Saha MN, Chattopadhyay D, et al. Large-scale degumming of ramie fibre using a newly isolated Bacillus pumilus DKS I with high pectate lyase activity[J]. Journal of Industrial Microbiology and Biotechnology, 2009, 36(2): 239-245. 被引量:1
  • 8Sharma S, Mandhan RP, Sharma J. Pseudozyma sp. SPJ: an economic and eco-friendly approach for degumming of flax fibers[J]. World Journal of Microbiology and Biotechnology, 2011, 27(11): 2697-2701. 被引量:1
  • 9Zheng L, Du Y, Zhang J. Degumming of ramie fibers by alkalophilic bacteria and their polysaccharide-degrading enzymes[J]. Bioresource Technology, 2001, 78(1): 89-94. 被引量:1
  • 10Yuan P, Meng K, Shi P, et al. An alkaline-active and alkali-stable pectate lyase from Streptomyces sp. S27 with potential in textile industry[J]. Journal of Industrial Microbiology and Biotechnology, 2012,39(6): 909-915. 被引量:1

二级参考文献14

  • 1薛长湖,张永勤,李兆杰,李志军.果胶及果胶酶研究进展[J].食品与生物技术学报,2005,24(6):94-99. 被引量:94
  • 2PerezS, Rodridguez-Carvajal MA, Doco T. A complex plant cell wall polysaccharide: rhamnogalacturonan Ⅱ. A structure in quest of a function. Biochimie, 2003, 85: 109-121. 被引量:1
  • 3Bruhlmann F, Leupin M, Erismann KH, et al. Enzymatec degumming of ramie bast fibers. J Biotechnol, 2000, 76: 43-50. 被引量:1
  • 4Zhang J, Henriksson G, Johansson G. Polygalacturonase is the key component in enzymatic retting of flax. J Biotechnol, 2000, 81: 85-891. 被引量:1
  • 5Kluskens LD, van Alebeek GJWM, Voragen AGJ, et al. Molecular and biochemical characterization of the thermoactive family 1 pectate lyase from the hyperthermophilic bacterium Thermotoga maritirna. J Biochem, 2003, 370: 651-659. 被引量:1
  • 6Shao WL, Wu HW, Pei JJ. Novel expression vector system regulated by sigma32 and methods for using it to produce recombinant protein: US patent, US 2007/ 0254335A1. 2007-11-07. 被引量:1
  • 7Sambrook J, Frisch F, Maniatis T. Molecular Cloning: A Laboratory Manual. 2nd Ed. New York: Cold Spring Harbor Laboratory Press, 1989. 被引量:1
  • 8Zhao QX, Yuan S, Zhang YL, et al. Expression, purification and characterization of pectate lyase A from Aspergillus nidulans in Escherichia coil World J Microbiol Biotechnol, 2007, 23: 1057-1064. 被引量:1
  • 9Macmillan JD, Vaughn RH. Purification and properties of a polygalacturonic acid-trans-eliminase produced by Clostridium multifermentans. J Biochem, 1964, 3: 564-572. 被引量:1
  • 10Collmer A, Ried JL, Mount MS. Assay methods for pectic enzymes. Methods Enzymol, 1988, 161: 329-335. 被引量:1

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