Abstract
Cutinase is a kind of multifunctional hydrolase, which has important application value in the food processing and textile refining industry. The recombinant expression system of Escherichia coli (E.coli) BL21 (DE3) was used to achieve the recombinant expression of Humicola insolens cutinase in E.coli, and the activity of extracellular supernatant in shaking flask level reached 170 U/mL. The recombinant cutinase was characterized. The optimum pH was 8.5, the optimum temperature was 80 ℃, with good pH stability and temperature stability. In order to further improve the possibility of the industrial application of H.insolens cutinase, the recombinant E.coli was cultured in 3 L fermentor and the cultivation condition is optimized. The optimum fermentation conditions: maintain pH 7.0 and 37 ℃ in early culture phases about 12~14 h; when the cell concentration OD600 up to 50, fermentation entered induced phases,adjust the temperature to 30 ℃, 0.2 g/(L·h) lactose solution were added with constant flow rate. The total fermentation period was about 36 h. The highest activity of enzyme reached to 2 233 U/mL, which is 13 times about the enzyme activity in shake flask level.
Publication Date
4-28-2018
First Page
1
Last Page
5
DOI
10.13652/j.issn.1003-5788.2018.04.001
Recommended Citation
Yirong, SUN; Jing, WU; and Lingqia, SU
(2018)
"Expression of Humicola insolens Cutinase in Escherichia coli and its Optimization of Fermentation,"
Food and Machinery: Vol. 34:
Iss.
4, Article 1.
DOI: 10.13652/j.issn.1003-5788.2018.04.001
Available at:
https://www.ifoodmm.cn/journal/vol34/iss4/1
References
[1] CHEN Sheng, TONG Xing, WOODARD R W, et al. Identification and characterization of bacterial cutinase[J]. J Biol Chem, 2008, 283(38): 25 854-25 862.
[2] 李江华, 刘龙, 陈晟, 等. 角质酶的研究进展[J]. 生物工程学报, 2009, 25(12): 1 829-1 837.
[3] FETT W F, GRARD H C, MOREAU R A. Cutinase production by Streptomyces spp[J]. Curr Microbiol, 1992, 25(3): 165-171.
[4] JOHAN S. Laundry detergent and/or fabric care compositions comprising a modified transferase: US, 6410498[P]. 2002-06-25.
[5] CHEN Sheng, SU Ling-qia, CHEN Jian, et al. Cutinase: characteristics, preparation, and application[J]. Biotechnology Advances, 2013, 31(8): 1 754-1 767.
[6] LOOMER S, ADLERCREUTZ P, MATTIASSON B. Triglyceride interesterification by lipases 1: Cocoa butter equivalents from a fraction of palm oil[J]. J Am Oil Chem Soc, 1990, 67: 519-524.
[7] KOLATTUKKUDY P E P R E, MAITI I B. Cutinases from fungi and pollen[J]. Methods Enzymol, 1981, 71(81): 652-664.
[8] MANDY A M A H, WOLFGANG Z. Cutinase production by Fusarium oxysporum in liquid medium using central composite design[J]. Biotechnol Lett, 2006, 28(1): 681-685.
[9] LI Dong, ASHBY A M, JOHNSTONE K. Molecular evidence that the extracellular cutinase Pbc1 is required for pathogenicity of Pyrenopeziza brassicae on oil seed rape[J]. Mol Plant Microbe Interact, 2003, 16(6): 545-552.
[10] SEBASTIAN J C A K, KOLATTUKKUDY P E. Discovery of a cutinase-producing Pseudomonas sp. cohabiting with an apparently nitrogen-fixing Corynebacterium sp. in the phyllosphere[J]. J Bacteriol, 1987, 169(1): 131-136.
[11] CORREA A, OPPEZZO P. Tuning different expression parameters to achieve soluble recombinant proteins in E. coli: advantages of high-throughput screening[J]. Biotechnol J., 2011, 6(6): 715-730.
[12] 姜琪, 宿玲恰, 吴敬, 等. 共表达磷脂酶 C 促进葡萄糖异构酶在大肠杆菌中的胞外表达[J]. 食品与生物技术学报, 2017, 36(3): 236-242.