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重组巨大芽孢杆菌产青霉素G酰化酶发酵条件研究 被引量:9

Studies on fermentation conditions for penicillin G acylase production with a recombinant Bacillus megaterium system
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摘要 对重组巨大芽孢杆菌产胞外青霉素G酰化酶的发酵条件进行优化。先用单因素实验确定最适碳源、氮源以及碳源浓度、氮源浓度、发酵时间和发酵温度的范围。采用Box-Behnken实验设计和响应面分析方法,对重组巨大芽孢杆菌产青霉素G酰化酶的发酵条件进行优化,得出其最佳发酵条件为:葡萄糖32 g/L、胰蛋白胨17 g/L、时间42.5 h、温度34℃,在此条件下青霉素G酰化酶的活力达到10 614±8 U/L,较优化前提高了16.83%。 The fermentation conditions for extracellular penicillin G acylase producted by recombinant Bacillusmegaterium were optimized. At first, the optimal carbon, nitrogen and the range of carbon concentration, nitrogen concentration, fermentation temperature and fermentation time were determined by single factor experiments. The experiment used the Box-Behnken experimental design and response surface analytical methodology to optimize the fermentation conditions of production of penicillin G acylase of recombinant Bacillus megaterium. The optimum fermentation conditions were obtained: glucose 32 g/L, tryptone 17 g/L , time 42.5 hours, temperature 34 ℃. Under these conditions, the activity of penicillin G aeylase was 10 614±8 U/L, being increased by 16. 83% compared with 16. 83% before optimization.
出处 《中南林业科技大学学报》 CAS CSCD 北大核心 2011年第7期124-129,135,共7页 Journal of Central South University of Forestry & Technology
基金 中南林业科技大学研究生科技创新基金项目(2009SX04)
关键词 重组巨大芽孢杆菌 青霉素G酰化酶 Box-Behnken实验设计 响应面法 发酵条件 recombinant Bacillus megaterium penicillin G acylase Box-Behnken experimental design response surface methodology fermentation conditions
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参考文献12

  • 1Kallenberg A I, Rantwijk F V, Sheldon R A. Immobilization of Penieillin G Aeylase: The Key to Optimum Performance [J]. Advanced Synthesis and Catalysis, 2005, 347: 905-926.
  • 2Rajendhran, Gunasekaran P. Recent Biotechnological Interventions for Devloping Improved Penicillin G Aeylases[J]. Journal of Bioscience and Bioengineering, 2004, 97: 1-13.
  • 3Arroyo M, Mata I, Aeebal C, et al. Bioteehnological applications of penicillin acylases: state-of-the-art[J] Applied Micro- biology Biotechnology, 2003, 60: 507-514.
  • 4Bruggink A, Roos E C, Vroom E D. Penicillin aeylase in the industrial production of betalactam antibiotics[J]. Organic Process Research and Development, 1998, 2: 128-133.
  • 5Vroom E D. The central role of penicillin acylase in antibiotics productlon[J]. Chimica Oggi-Chemistiy Today, 1999, 17~ 65 -68.
  • 6Mahajan P B. Penicillin aeylase[J]. Applied Biochemistry and Bioteehnology, 1984, 9: 537-554.
  • 7Shewale J G, H Sivaraman. Penicillin aeylase, Enzyme production and its application in the manufacture of 6-APA[J]. Process Biochemistry, 1989, 8: 146-154.
  • 8Mheen S, Ham Studies on microbiol penicillin amidase: (IV) the production of penicillin amidase from Bacillus megaterium [J]. Journal of General Microbiology, 1982, 28: 281-291.
  • 9口如琴,褚西宁,袁静明.巨大芽孢杆菌产青霉素酰化酶发酵条件的研究[J].山西大学学报(自然科学版),1995,18(4):432-435. 被引量:1
  • 10Pramod B Mahajan. Penicillin acylase[J]. Applied Biochemistry and Biotechnology, 1984, (9) : 537-554.

二级参考文献40

  • 1周蓓芸,王峥,孔德育,郑幼霞.热稳定β-淀粉酶高产菌株选育及发酵条件研究[J].生物工程学报,1994,10(3):258-262. 被引量:6
  • 2彭平,吴襟,程安春,高启禹,张树政.芽孢杆菌α-淀粉酶基因的克隆、表达和酶学性质分析[J].微生物学报,2005,45(6):876-880. 被引量:6
  • 3XU Zhi—nan(徐志南) CEN Pei—lin(岑沛霖) Wong W K R.The effects ofdifferent glucose feeding modes on hEGF production in an excretory recombinant Escherichia coli K12 sytem(不同流加发酵方式对重组大肠杆菌细胞外表达水平的影响)[J].Chinese J Bloteehnol(生物工程学报),2001,17(5):594-598.
  • 4Bruggink A, Roos E C, Vroom E. Penicillin acylase in the industrial production of β-lactam antibiotics [J]. Organic Process Research & Development, 1998, 2(2): 128-133.
  • 5Chou C P, Wong W C, Liu M I. An approach for enhancing heterologous production of Providenica rettgeri penicillin acylase in Escherichia coli [J]. Biotecnol Prog 2000, 16, 315-318.
  • 6Meevootisom V, Saunders J R. Cloning and expression of penicillin acylase genes from overproducing strains of Escherichia coli and Bacillus megaterium [J]. Appl Microhiol Biotechnol. 1987, 25: 372-378.
  • 7Kang J H, Hwang Y, Yoo O J. Expression of penicillim G acylase gene from Bacillus megaterium ATCC 14945 in Escherichia coli and Bacillus subtilis [J]. J Biotech, 1991, 17(2): 99-108.
  • 8Samrook J, Fritsch E F, Maniaatis T. Molecular Cloning: A Laboratory Manual, 2^nd ed [M]. New York: Cold Spring Harbor Laboratory Press, 1989.
  • 9Chou C P, Tseng J H, Lin M I. Manipulation of carbon assimilation with respect to expression of the pac gene for improving production of penicillin acylase in Escherichia coli [J]. Journal of Biotechnology, 1999, 69: 27-38.
  • 10Schumacher G, Sizmann D, Haug H. Penicillin acylase from Escherichia coli: Unique gene-protein relation [J]. Nucleic Acid Research, 1986, 14: 5713-5727.

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