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耐受有机溶剂洋葱伯克霍尔德菌ZYB002全细胞脂肪酶酶学性质 被引量:3

Properties of Whole-cell Lipase from Burkholderia sp.ZYB002 with Organic Solvent Tolerance
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摘要 一株对多种有机溶剂具有良好耐受能力的产脂肪酶菌株ZYB002经分子鉴定为洋葱伯克霍尔德菌。其产生的细胞结合脂肪酶最适温度为65°C,最适pH为8.0,在低于70°C和pH3-8.5的范围内,全细胞脂肪酶保持稳定。Ca2+、K+、Na+和NO3-等离子对脂肪酶活性有激活作用,而Zn2+有抑制效应。全细胞脂肪酶对正丁醇有较强的耐受能力,但曲拉通X-100对脂肪酶活性有强烈的抑制效应。洋葱伯克霍尔德菌ZYB002全细胞脂肪酶良好的碱稳定性、热稳定性和有机溶剂耐受性,表明该全细胞脂肪酶具有重要的工业应用潜力。 The lipase-producing strain ZYB002 with broad-spectrum organic solvent-tolerance was identi- fied as Burkholderia cepacia complex by the recA sequence. The optimal pH and temperature for lipolytic activity of the cell-bound lipase from Burkholderia sp. ZYBO02 was 8.0 and 65℃, respectively. It was stable at temperature up to 70℃ and retained 79.2% of its original activity for 1 h. The lipase was highly stable in the pH range from 3.0 to 8.5 for 6 h. Ca^2+, K^+, Na^+, NO3^-, etc. ions stimulated its lipolytic activity, whereas Zn^2+ ions caused inhibition. The cell-bound lipase was also relatively stable in n-butanol at a final concentration of 50% (V/V) for 24 h. However, the lipase was strongly inhibited in triton X-100 at a final concentra-tion of 10% (V/V). The cell-bound lipase with thermal resistance, alkaline resistance and organic solvent resistance showed its' great potential in various industrial application fields.
出处 《微生物学通报》 CAS CSCD 北大核心 2010年第1期2-6,共5页 Microbiology China
基金 国家863计划资助项目(No2007AA100703) 国家自然科学基金资助项目(No30870545) 福建省自然科学基金(杰青)资助项目(No2009J06013)
关键词 洋葱伯克霍尔德菌 有机溶剂耐受性 全细胞脂肪酶 酶学性质 Burkholderia sp., Organic solvent tolerance, Whole-cell lipase, Biochemical characterization
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参考文献12

  • 1Hasan F, Shah AA, Hameed A. Industrial applications of microbial lipases. Enzyme and Microbial Technology, 2006, 39(2): 235-251.
  • 2Rahman RN, Baharum SN, Basri M, et al. High-yield purification of an organic solvent-tolerant lipase from Pseudomonas sp. strain S5. Analytical Biochemistry, 2005,341(2): 267-274.
  • 3El Abbadi N, Druet D, Comeau LC. Immunocytochemical identification and localization of lipase in cells of the mycelium of Penicillium cyclopium variety. Applied Microbiology and Biotechnology, 1995, 42(6): 923-930.
  • 4Ishige T, Honda K, Shimizu S. Whole organism biocatalysis. Current Opinion in Chemical Biology, 2005, 9(2): 174-180.
  • 5De Bont JAM. Solvent-tolerant bacteria in biocatalysis. Trends in Biotechnology, 1998, 16(12): 493-499.
  • 6Pencreac'h G, Leullier M, Baratti JC. Properties of free and immobilized lipase from Pseudomonas cepacia. Biotechnology and Bioengineering, 1997, 56(2): 181-189.
  • 7Tomic S, Ramek M. Quantum mechanical study of Burkholderia cepacia lipase enantioselectivity. Journal of Molecular Catalysis B: Enzymatic, 2006, 38(3/6): 139-147.
  • 8Yu L J, Xu Y, Wang XQ, et al. Highly enantioselective hydrolysis of DL-menthyl acetate to L-menthol by whole-cell lipase from Burkholderia cepacia ATCC 25416 Journal of Molecular Catalysis B: Enzymatic, 2007, 47(3/4): 149-154.
  • 9Mahenthiralingam E, Campbell ME, Foster J, et al. Random amplified polymorphic DNA typing of Pseudomonas aeruginosa isolates recovered from patients with cystic fibrosis. Journal of Clinical Microbiology, 1996, 34(5): 1129-1135.
  • 10Payne GW, Vandamme P, Morgan SH, et al. Development of a reeA gene-based identification approach for the entire Burkholderia genus. Applied and Environmental Microbi- ology, 2005, 71(7): 3917-3927.

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