Please wait a minute...

中国生物工程杂志

CHINA BIOTECHNOLOGY
中国生物工程杂志  2014, Vol. 34 Issue (3): 56-60    DOI: 10.13523/j.cb.20140308
研究报告     
bmy基因敲除对解淀粉芽孢杆菌Q-426溶血性及抗菌活性的影响
陶思美1,2, 郑维1,2, 赵朋超3, 周伟1,2, 权春善1,2, 范圣第1,2
1. 大连民族学院生命科学学院 大连 116600;
2. 国家民委教育部重点实验室 大连 116600;
3. 河南科技大学医学技术与工程学院 洛阳 471023
Effects of bmy Gene knockout on Hemolysis and Antifungal activity of Bacillus amyloliquefaciens Q-426
TAO Si-mei1,2, ZHENG Wei1,2, ZHAO Peng-chao3, ZHOU Wei1,2, QUAN Chun-shan1,2, FAN Sheng-di1,2
1. Department of Life Science, Dalian Nationalities University, Dalian 116600, China;
2. SEACME Key laboratory, Dalian 116600, China;
3. Department of Medical Technology and Engineering, Henan University of Science and Technology, Luoyang 471003, China
 全文: PDF(588 KB)   HTML
摘要: Iturin家族环脂肽对于红色毛癣菌等病原真菌具有较强的抑菌活性,有潜力成为治疗皮肤疾病的新型抗真菌药物。解淀粉芽孢杆菌Q-426菌株能够产生环脂肽fengycins和iturin家族的bacillomycin D,但该菌株发酵液具有溶血活性。为确定bacillomycin D是否为引发溶血作用的主要物质,本文利用同源重组基因敲除技术,构建解淀粉芽孢杆菌bmy基因缺失菌株,抑制bacillomycin D的合成,研究对其溶血性及抗菌活性的影响。突变菌株发酵液中未检测到bacillomycin D产生,且发酵液的溶血性及抗菌活性明显减小,表明bacillomycin D与该菌的溶血活性及抑菌活性密切相关。
关键词: 环脂肽基因敲除bmy基因溶血性抗菌活性    
Abstract: Iturin family of lipopeptides has strong antifungal activity against pathogenic fungi such as Trichophyton rubrum and has potential to become a new antifungal drug currently used against dermatophytes. Bacillus amyloliquefaciens Q-426 could produce fengycins and bacillomycin D (a member of iturin family), and its fermentation broth shows a hemolytic activity. In order to determine whether bacillomycin D is the main hemolytic substances, a homologous recombinantion gene knockout technology was used to construct strain Q-426-Δ-bmy. Bacillomycin D was not detected in the Q-426-Δ-bmy strain fermentation broth, and there was a significant reduction in the hemolysis and antifungal activity in contrast with wild strain Q-426, indicating that bacillomycin D is closely related to hemolytic activity and antifungal activity of Bacillus amyloliquefaciens Q-426.
Key words: Cyclic lipopeptides    Gene knockout    bmy gene    Hemolysis    Antifungal activity
收稿日期: 2013-12-17 出版日期: 2014-03-25
ZTFLH:  Q78  
基金资助: 辽宁省教育厅重点实验室资助项目(LS2010049)
通讯作者: 权春善     E-mail: mikyeken@dlnu.edu.cn
服务  
把本文推荐给朋友
加入引用管理器
E-mail Alert
RSS
作者相关文章  
陶思美
郑维
赵朋超
周伟
权春善
范圣第

引用本文:

陶思美, 郑维, 赵朋超, 周伟, 权春善, 范圣第. bmy基因敲除对解淀粉芽孢杆菌Q-426溶血性及抗菌活性的影响[J]. 中国生物工程杂志, 2014, 34(3): 56-60.

TAO Si-mei, ZHENG Wei, ZHAO Peng-chao, ZHOU Wei, QUAN Chun-shan, FAN Sheng-di. Effects of bmy Gene knockout on Hemolysis and Antifungal activity of Bacillus amyloliquefaciens Q-426. China Biotechnology, 2014, 34(3): 56-60.

链接本文:

https://manu60.magtech.com.cn/biotech/CN/10.13523/j.cb.20140308        https://manu60.magtech.com.cn/biotech/CN/Y2014/V34/I3/56

[1] 牛力轩, 王楠, 王雪梅, 等. 一株产脂肽类抗生素bacillopeptin A深海芽孢杆菌的筛选与鉴定. 中国抗生素杂志, 2011, 36(10): 738-750. Niu L X, Wang N, Wang X M, et al. Screening and identification of a deep-sea derived Bacillus sp. Producing lipopeptidebacillopeptin A. Chinese Journal of Antibiotics, 2011, 36(10): 738-750.
[2] Zheng G, Slavik M F. Isolation, partial purification and characterization of a bacteriocin produced by a newly isolated Bacillus subtilis strain. Lett Appl Microbiol, 1999, 28(5): 363-367.
[3] Chen X H, Koumoutsi A, Scholz R, et al. Genome analysis of Bacillus amyloliquefaciens FZB42 reveals its potential for biocontrol of plant pathogens. Journal of Biotechnology, 2008, 140(1-2): 27-37.
[4] Aperce C C, Burkey T E, KuKanich B, et al. Interaction of Bacillus species and Salmonella enterica serovar Typhimurium in immune or inflammatory signaling from swine intestinal epithelial cells. J Anim Sci, 2010, 88(5): 1649-1656.
[5] Cotta S R, da Mota F F, Tupinambá G, et al. Antimicrobial activity of Paenibacillus kribbensis POC 115 against the dermatophyte Trichophyton rubrum. World J Microbiol Biotechnol, 2012, 28: 953-962.
[6] Jennings M B, Weinberg J M, Koestenblatt E K, et al. Study of clinically suspected onychomycosis in a podiatric population. J Am Podiatr Med Assoc, 2002, 92 (6): 327-330.
[7] Zhao P C, Quan C S, Wang Y G, et al. Bacillus amyloliquefaciens Q-426 as a potential biocontrol agent against Fusarium oxysporum f. Sp. Spinaciae. J Basic Microbiol, 2013, doi: 10. 1002/jobm. 201200414.
[8] 刁兆玉, 成鹏, 王仲妮. 表面活性剂溶血作用的研究进展. 食品与药品, 2010, 12(3): 125-129. Diao Z Y, Cheng P, Wang Z N. Progress on Hemolytic Action of Surfactants. Food and Drug, 2010, 12(3): 125-129.
[9] 赵朋超, 权春善, 金黎明, 等. 氮源和碳源对解淀粉芽孢杆菌Q-426抗菌脂肽 合成的影响. 中国生物工程杂志, 2012, 32(10): 50-56. Zhao P C, Quan C S, Jin L M, et al. Effects of Different Nitrogen and Carbon Sources on the Production of Antifungal Lipopeptides from Bacillus amyloliquefaciens Q-426. China Biotechnology, 2012, 32(10): 50-56.
[10] Valérie L, Romain M, Max B, et al. The lipopeptides mycosubtilin and surfactin enhance spreading of Bacillus subtilis strains by their surface-active properties. Arch Microbiol, 2006, 186: 475-483.
[11] Matsuyama T, Kaneda k, Nakagawa Y, et al. A novel extracellular cyclic lipopeptide which promotes flagellum-dependent and -independent spreading growth of Serratia marcescens. J Bacteriol, 1992, 174(6):1769-1776.
[12] Isabelle V G, Alexey N, Luis A, et al. Association of hemolytic activity of Pseudomonas entomophila, a versatile soil bacterium, with cyclic lipopeptide production. Applied and Enivironmental Microbiology, 2010, 76(3): 910-921.
[1] 彭海丽,侯占铭. MDT1基因参与禾谷镰刀菌分生孢子发生和营养生长 *[J]. 中国生物工程杂志, 2020, 40(8): 10-18.
[2] 郭洋,万颖寒,王珏,龚慧,周宇,慈磊,万志鹏,孙瑞林,费俭,沈如凌. Toll样受体4(TLR4)基因剔除小鼠构建及初步表型分析[J]. 中国生物工程杂志, 2020, 40(6): 1-9.
[3] 郭晶,侯占铭. Folpcs1基因对尖孢镰刀菌亚麻专化型的无性繁殖和营养生长的调控 *[J]. 中国生物工程杂志, 2020, 40(3): 48-64.
[4] 郭胜楠, 李信晓, 王峰, 刘昆梅, 丁娜, 扈启宽, 孙涛. 海马与新皮质组织特异性GABRG2基因敲除小鼠模型的构建及其在遗传性癫痫伴热性惊厥附加症中的初步研究 *[J]. 中国生物工程杂志, 2020, 40(3): 9-20.
[5] 郭超婧,朱琼,张新,李磊,张令强. 去泛素化酶OTUB1肝脏特异性基因敲除小鼠模型的构建与表型分析 *[J]. 中国生物工程杂志, 2019, 39(5): 80-87.
[6] 万颖寒,慈磊,王珏,龚慧,李俊,董茹,孙瑞林,费俭,沈如凌. PD-L1基因敲除小鼠构建及初步表型验证[J]. 中国生物工程杂志, 2019, 39(12): 42-49.
[7] 吴果果,宋淑婷,岳荣,张晶,关莹,王玥,刘宝爱,吕学敏,魏建军,张会图. 反向筛选标记基因upp在杀真菌链霉菌遗传改造中的应用 *[J]. 中国生物工程杂志, 2019, 39(11): 78-86.
[8] 陆海燕,李佳蔓,孙思凡,章小毛,丁娟娟,邹少兰. CRISPR - Cas9系统介导的工业酵母营养缺陷型菌株构建 *[J]. 中国生物工程杂志, 2019, 39(10): 67-74.
[9] 苏春晓,张晓玉,曾晗,陈压西,阮雄中,杨萍. 肝脏特异性CD36基因敲除小鼠的制备及鉴定 *[J]. 中国生物工程杂志, 2018, 38(8): 26-33.
[10] 戴红苗,付业胜,张令强. 应用CRISPR/Cas9技术构建YOD1基因敲除小鼠 *[J]. 中国生物工程杂志, 2018, 38(6): 52-57.
[11] 戈家傲,刘畅,龚建刚,刘艳琴. 抗菌环肽的研究进展 *[J]. 中国生物工程杂志, 2018, 38(11): 76-83.
[12] 盛玉瑞,李斌,王斌,左娣,马琳,任晓璠,郭乐,刘昆梅. 利用CRISPR/Cas9技术构建AEG-1基因敲除U251细胞系并探讨其转移行为的特点 *[J]. 中国生物工程杂志, 2018, 38(10): 38-47.
[13] 孙一平, 王越, 金镇, 王晓岩, 孙磊, 张璇, 冯冲, 周效华. SHBG基因敲除小鼠模型的建立及其表型分析[J]. 中国生物工程杂志, 2017, 37(8): 39-45.
[14] 张震阳, 杨艳坤, 战春君, 李翔, 刘秀霞, 白仲虎. Pichia pastoris X-33 ΔGT2缓解甘油对AOX1的阻遏并用于外源蛋白的高效表达[J]. 中国生物工程杂志, 2017, 37(1): 38-45.
[15] 杜红燕, 李天明, 刘金雷, 冯惠勇. 构建尿嘧啶磷酸核糖转移酶基因缺失菌株实现Gluconobacter suboxydans基因组无痕修饰[J]. 中国生物工程杂志, 2016, 36(7): 64-71.