研究报告

甜蛋白Brazzein在毕赤酵母中的表达及应用

  • 孟珊珊 ,
  • 谭明 ,
  • 肖冬光 ,
  • 宋诙
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  • 1(天津科技大学 生物工程学院,天津,300457)
    2(中国科学院 天津工业生物技术研究所,天津,300308
硕士研究生(宋诙研究员为通讯作者,E-mail:song_h@tib.cas.cn)

收稿日期: 2020-03-13

  修回日期: 2020-04-14

  网络出版日期: 2020-08-15

Expression of sweet protein Brazzein in Pichia pastoris and its application

  • MENG Shanshan ,
  • TAN Ming ,
  • XIAO Dongguang ,
  • SONG Hui
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  • 1(Institute of Biological Engineering,Tianjin University of Science and Technology,Tianjin 300457,China)
    2(Tianjin Institute of Industrial Biotechnology,Chinese Academy of Sciences,Tianjin 300308,China)

Received date: 2020-03-13

  Revised date: 2020-04-14

  Online published: 2020-08-15

摘要

巴西甜蛋白(Brazzein)是分离自非洲西部野生植物Pentadiplandra brazzeana Baillon果实中的一种天然高倍甜味蛋白,具有较好的食品应用潜力。利用毕赤酵母GS115对巴西甜蛋白及蛋白二硫键异构酶(protein disulfide isomerase,PDI)进行共表达,重组Brazzein在发酵液中分泌表达量为1 g/L。采用超滤-纳滤膜分离系统和冷冻干燥技术开发重组Brazzein的低成本制备工艺,并完成口感评价,甜度倍数为蔗糖的40倍。同时研究了重组Brazzein对常见致病菌和肠道益生菌的体外抑菌性能,结果表明,重组Brazzein对白念珠菌的最低抑菌质量浓度(minimum inhibitory concentration,MIC)为15 mg/mL,对金黄色葡萄球菌的MIC值为7.5 mg/mL,对桧状青霉的MIC值为3.75 mg/mL,对枯草芽孢杆菌、大肠杆菌、干酪乳杆菌、嗜酸乳杆菌和粪肠球菌没有发现明显的抑菌效果。该研究为Brazzein在甜味剂方面的推广应用提供了理论研究基础。

本文引用格式

孟珊珊 , 谭明 , 肖冬光 , 宋诙 . 甜蛋白Brazzein在毕赤酵母中的表达及应用[J]. 食品与发酵工业, 2020 , 46(15) : 21 -26 . DOI: 10.13995/j.cnki.11-1802/ts.023943

Abstract

Brazzein is a kind of natural high-sweetness protein isolated from the fruit of wild plant Pentadiplandra brazzeana Baillon in western Africa and has good food application potential. Using Pichia pastoris GS115 to co-express Brazzein and protein disulfide isomerase (PDI),the expression of recombinant Brazzein in the fermentation broth was 1 g/L. An ultrafiltration-nanofiltration membrane separation system and freeze-drying technology were used to develop a low-cost preparation process for recombinant Brazzein. The taste evaluation of recombinant Brazzein was conducted. The sweetness of Brazzein was 40 times of sucrose. In vitro antibacterial performance of recombinant Brazzein against common pathogenic bacteria and intestinal probiotics was studied. The results showed that the recombinant Brzezein had a minimum inhibitory concentration (MIC) value of 15 mg/mL against Candida albicans and 7.5 mg/mL against Staphylococcus aureus. The MIC value for Penicillium spis was 3.75 mg/mL and no obvious antibacterial effect was found on Bacillus subtilis,Escherichia coli,Lactobacillus casei,Lactobacillus acidophilus and Enterococcus faecalis. It provides a theoretical basis for the popularization and application of Brazzein in sweetener.

参考文献

[1] KANT R.Sweet proteins-potential replacement for artificial low calorie sweeteners[J].Nutrition Journal,2005,4(5):5-10.
[2] MOORADIAN A D,SMITH M,TOKUDA M.The role of artificial and natural sweeteners in reducing the consumption of table sugar: A narrative review[J].Clinical Nutrition ESPEN,2017,18(1):1-8.
[3] MASUDA T,KITABATAKE N.Developments in biotechnological production of sweet proteins[J].Journal of Bioscience and Bioengineering,2006,102(5):375-389.
[4] WINTJENS R,VIET T M,MBOSSO E,et al.Hypothesis/review: the structural basis of sweetness perception of sweet-tasting plant proteins can be deduced from sequence analysis[J].Plant Science,2011,181(4):347-354.
[5] ASSADI-PORTER F M,ACETI D J,CHENG H,et al. Efficient production of recombinant Brazzein,a small,heat-stable,sweet-tasting protein of plant origin[J].Archives of Biochemistry and Biophysics,2000,376(2):252-258.
[6] MING D,HELLEKANT G.Brazzein,a new high-potency thermostable sweet protein from Pentadiplandra brazzeana B[J].FEBS Letters,1994,355(1):106-108.
[7] FAUS I.Recent developments in the characterization and biotechnological production of sweet-tasting proteins[J].Applied Microbiology and Biotechnology,2000,53(2):145-151.
[8] CALDWELL J E,ABILDGAARD F,DZAKULA Z,et al.Solution structure of the thermostable sweet-tasting protein Brazzein[J].Nature Structural Biology,1998,5(6):427-431.
[9] NAGATA K,HONGO N,KAMEDA Y,et al.The structure of Brazzein,a sweet-tasting protein from the wild Africanplant Pentadiplandra brazzeana[J].Acta Crystallographica. Section D:Biological Crystallography,2013,69(4):642-647.
[10] CHUNG J H,KONG J N,CHOI H E,et al.Antioxidant,anti-inflammatory,and anti-allergic activities of the sweet-tasting protein Brazzein[J].Food Chemistry,2018,267(30):163-169.
[11] YOUNT N Y,YEAMAN M R.Multidimensional signatures in antimicrobial peptides[J].Proceedings of the National Academy of Sciences of the United States of America,2004,101(19):7 363-7 368.
[12] 王燕. 农杆菌介导甜蛋白Brazzein基因转化‘章姬’草莓的研究[D].南京:南京农业大学,2012.
[13] 高逸群.甜味蛋白(Brazzein)大肠杆菌表达系统的建立[D].长春:吉林大学,2006.
[14] 刘松财,张永亮,任晓慧,等.甜味蛋白(Brazzein)基因的人工合成及其在大肠杆菌中的重组表达[J].中国兽医学报,2006,26(5):538-540.
[15] 王长远,张丽萍,刘松财,等.甜味蛋白Brazzein在毕赤氏酵母中表达的初步研究[J].中国食品学报,2009,9(5):43-48.
[16] 李春丽,何国庆,阮晖,等.des-pGlu1-Bra基因的人工合成及其在大肠杆菌中的重组表达[J].农业生物技术学报,2005,13(1):38-41.
[17] 赵红玲,陈劲春.利用毕赤酵母表达植物甜蛋白(Brazzein)的初步研究[J].北京化工大学学报(自然科学版),2005,32(2):14-16;20.
[18] ASSADI-PORTER F M,ACETI D J,MARKLEY J L.Sweetness determinant sites of Brazzein,a small,heat-stable,sweet-tasting protein[J].Archives of Biochemistry and Biophysics,2000,376(2):259-265.
[19] 丁鸣,胡忠.耐热甜味蛋白Brazzein的特性和化学修饰[J].云南植物研究,1996,18(2):123-133.
[20] 顾园,诸欣平,王少华.毕赤酵母表达蛋白质的糖基化[J].生命的化学,2004,24(4):353-355.
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