• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

在枯草芽孢杆菌 WB700 中高效生物合成 Cecropin A-melittin 突变体。

Efficient biosynthesis of a Cecropin A-melittin mutant in Bacillus subtilis WB700.

机构信息

Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing 100094, China.

College of Animal Science and Technology, Northwest A&F University, Yangling, Shaanxi 712100, China.

出版信息

Sci Rep. 2017 Jan 10;7:40587. doi: 10.1038/srep40587.

DOI:10.1038/srep40587
PMID:28071737
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5223193/
Abstract

The efficient production of antimicrobial peptides (AMPs) for clinical applications has attracted the attention of the scientific community. To develop a novel microbial cell factory for the efficient biosynthesis of a cecropin A-melittin mutant (CAM-W), a recombinant Bacillus subtilis WB700 expression system was genetically modified with a novel vector, including a fusion gene encoding CAM-W, the autoprotease EDDIE and the signal peptide SacB under the control of the maltose-inducible promoter P. A total of 159 mg of CAM-W was obtained from 1 L of fermentation supernatant. The purified CAM-W showed a consistent size with the expected molecular weight of 3.2 kDa. Our findings suggest that this novel expression system can be used as a powerful tool for the efficient production of CAM-W.

摘要

抗菌肽(AMPs)的高效生产引起了科学界的关注。为了开发一种新型的微生物细胞工厂,用于高效生物合成 Cecropin A-Melitlin 突变体(CAM-W),我们对重组枯草芽孢杆菌 WB700 表达系统进行了基因修饰,使用了一种新型载体,其中包括融合基因 CAM-W、自蛋白酶 EDDIE 和信号肽 SacB,它们受麦芽糖诱导型启动子 P 的控制。从 1L 发酵上清液中获得了 159mg 的 CAM-W。纯化后的 CAM-W 与预期的 3.2kDa 分子量一致。我们的研究结果表明,这种新型表达系统可以作为高效生产 CAM-W 的有力工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/475a/5223193/c279b5720475/srep40587-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/475a/5223193/7dda0a8f2cd0/srep40587-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/475a/5223193/de2e96202513/srep40587-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/475a/5223193/c279b5720475/srep40587-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/475a/5223193/7dda0a8f2cd0/srep40587-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/475a/5223193/de2e96202513/srep40587-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/475a/5223193/c279b5720475/srep40587-f3.jpg

相似文献

1
Efficient biosynthesis of a Cecropin A-melittin mutant in Bacillus subtilis WB700.在枯草芽孢杆菌 WB700 中高效生物合成 Cecropin A-melittin 突变体。
Sci Rep. 2017 Jan 10;7:40587. doi: 10.1038/srep40587.
2
Maltose Induced Expression of Cecropin AD by SUMO Technology in Bacillus subtilis WB800N.苏嫝技术诱导枯草芽孢杆菌 WB800N 表达抗菌肽 Cecropin AD
Protein J. 2020 Aug;39(4):383-391. doi: 10.1007/s10930-020-09908-x.
3
Expression of plectasin in Bacillus subtilis using SUMO technology by a maltose-inducible vector.利用麦芽糖诱导型载体通过SUMO技术在枯草芽孢杆菌中表达plectasin。
J Ind Microbiol Biotechnol. 2015 Oct;42(10):1369-76. doi: 10.1007/s10295-015-1673-y. Epub 2015 Aug 25.
4
Novel expression vector for secretion of cecropin AD in Bacillus subtilis with enhanced antimicrobial activity.用于在枯草芽孢杆菌中分泌天蚕素AD并具有增强抗菌活性的新型表达载体。
Antimicrob Agents Chemother. 2009 Sep;53(9):3683-9. doi: 10.1128/AAC.00251-09. Epub 2009 Jun 22.
5
Pathogen-induced expression of a cecropin A-melittin antimicrobial peptide gene confers antifungal resistance in transgenic tobacco.病原体诱导的天蚕素A-蜂毒素抗菌肽基因表达赋予转基因烟草抗真菌能力。
J Exp Bot. 2005 Jun;56(416):1685-95. doi: 10.1093/jxb/eri165. Epub 2005 Apr 29.
6
[Screening of optimal signal peptide for heterologous xylanase secretion by Bacillus subtilis].[枯草芽孢杆菌异源分泌木聚糖酶的最佳信号肽筛选]
Wei Sheng Wu Xue Bao. 2011 Jul;51(7):979-83.
7
Cecropin A-melittin mutant with improved proteolytic stability and enhanced antimicrobial activity against bacteria and fungi associated with gastroenteritis in vitro.具有改良的蛋白水解稳定性和增强的抗细菌和真菌活性的 Cecropin A-melittin 突变体,可用于治疗与肠胃炎相关的细菌和真菌。
Biochem Biophys Res Commun. 2014 Sep 5;451(4):650-5. doi: 10.1016/j.bbrc.2014.08.044. Epub 2014 Aug 15.
8
A novel expression vector for the secretion of abaecin in Bacillus subtilis.一种用于在枯草芽孢杆菌中分泌阿贝菌素的新型表达载体。
Braz J Microbiol. 2017 Oct-Dec;48(4):809-814. doi: 10.1016/j.bjm.2017.01.009. Epub 2017 Jun 3.
9
High-level secretory production of intact, biologically active staphylokinase from Bacillus subtilis.从枯草芽孢杆菌中高效分泌产生完整的、具有生物活性的葡萄球菌激酶。
Biotechnol Bioeng. 1999 Jan 5;62(1):87-96.
10
[Transgenic Belarussian-bred potato plants expressing genes for antimicrobial peptides of the cecropin-melittin type].[表达天蚕素 - 蜂毒素型抗菌肽基因的白俄罗斯培育转基因马铃薯植株]
Genetika. 2010 Dec;46(12):1626-34.

引用本文的文献

1
Unlocking the power of antimicrobial peptides: advances in production, optimization, and therapeutics.释放抗菌肽的力量:生产、优化及治疗方面的进展
Front Cell Infect Microbiol. 2025 Apr 28;15:1528583. doi: 10.3389/fcimb.2025.1528583. eCollection 2025.
2
Establishment of the CRISPR-Cpf1 gene editing system in and multiplexed gene knockout.CRISPR-Cpf1基因编辑系统的建立及多重基因敲除
Synth Syst Biotechnol. 2024 Aug 8;10(1):39-48. doi: 10.1016/j.synbio.2024.08.002. eCollection 2025.
3
Hosts and Heterologous Expression Strategies of Recombinant Toxins for Therapeutic Purposes.

本文引用的文献

1
Molecular chaperones (TrxA, SUMO, Intein, and GST) mediating expression, purification, and antimicrobial activity assays of plectasin in Escherichia coli.分子伴侣(硫氧还蛋白、小泛素样修饰蛋白、内含肽和谷胱甘肽S-转移酶)介导的大肠埃希菌中plecatin的表达、纯化及抗菌活性测定
Biotechnol Appl Biochem. 2015 Sep-Oct;62(5):606-14. doi: 10.1002/bab.1303. Epub 2015 Jan 15.
2
Cecropin A-melittin mutant with improved proteolytic stability and enhanced antimicrobial activity against bacteria and fungi associated with gastroenteritis in vitro.具有改良的蛋白水解稳定性和增强的抗细菌和真菌活性的 Cecropin A-melittin 突变体,可用于治疗与肠胃炎相关的细菌和真菌。
Biochem Biophys Res Commun. 2014 Sep 5;451(4):650-5. doi: 10.1016/j.bbrc.2014.08.044. Epub 2014 Aug 15.
3
宿主和异源表达策略的重组毒素用于治疗目的。
Toxins (Basel). 2023 Dec 13;15(12):699. doi: 10.3390/toxins15120699.
4
An overview and future prospects of recombinant protein production in Bacillus subtilis.枯草芽孢杆菌中重组蛋白生产的概述及未来前景。
Appl Microbiol Biotechnol. 2021 Sep;105(18):6607-6626. doi: 10.1007/s00253-021-11533-2. Epub 2021 Sep 1.
5
Mitigation of peri-implantitis by rational design of bifunctional peptides with antimicrobial properties.通过具有抗菌性能的双功能肽的合理设计来减轻种植体周围炎。
ACS Biomater Sci Eng. 2020 May 11;6(5):2682-2695. doi: 10.1021/acsbiomaterials.9b01213. Epub 2019 Sep 24.
6
Expression of Melittin in Fusion with GST in and Its Purification as a Pure Peptide with Good Bacteriostatic Efficacy.蜂毒肽与谷胱甘肽 S-转移酶融合表达及其作为具有良好抑菌效果的纯肽的纯化
ACS Omega. 2020 Apr 13;5(16):9251-9258. doi: 10.1021/acsomega.0c00085. eCollection 2020 Apr 28.
7
Antifungal Peptides as Therapeutic Agents.抗真菌肽作为治疗剂。
Front Cell Infect Microbiol. 2020 Mar 17;10:105. doi: 10.3389/fcimb.2020.00105. eCollection 2020.
8
High copy number and highly stable Escherichia coli-Bacillus subtilis shuttle plasmids based on pWB980.基于 pWB980 的高拷贝数和高稳定性大肠杆菌-枯草芽孢杆菌穿梭质粒。
Microb Cell Fact. 2020 Feb 7;19(1):25. doi: 10.1186/s12934-020-1296-5.
9
Engineering Biology to Construct Microbial Chassis for the Production of Difficult-to-Express Proteins.工程生物学构建用于生产难表达蛋白的微生物底盘。
Int J Mol Sci. 2020 Feb 2;21(3):990. doi: 10.3390/ijms21030990.
10
Anti-amoebic activity of a cecropin-melittin hybrid peptide (CM11) against trophozoites of Entamoeba histolytica.抗菌肽 CM11 对溶组织内阿米巴滋养体的抗阿米巴活性。
Wien Klin Wochenschr. 2019 Sep;131(17-18):427-434. doi: 10.1007/s00508-019-01540-9. Epub 2019 Aug 26.
Recombinant polypeptide production in E. coli: towards a rational approach to improve the yields of functional proteins.在大肠杆菌中生产重组多肽:迈向提高功能蛋白产量的合理方法。
Microb Cell Fact. 2013 Nov 1;12:101. doi: 10.1186/1475-2859-12-101.
4
Construction and expression of an antimicrobial peptide scolopin 1 from the centipede venoms of Scolopendra subspinipes mutilans in Escherichia coli using SUMO fusion partner.利用SUMO融合伴侣在大肠杆菌中构建和表达来自少棘蜈蚣毒液的抗菌肽scolopin 1。
Protein Expr Purif. 2013 Dec;92(2):230-4. doi: 10.1016/j.pep.2013.10.004. Epub 2013 Oct 18.
5
Production of human antimicrobial peptide LL-37 in Escherichia coli using a thioredoxin-SUMO dual fusion system.利用硫氧还蛋白-SUMO双融合系统在大肠杆菌中生产人抗菌肽LL-37。
Protein Expr Purif. 2013 Feb;87(2):72-8. doi: 10.1016/j.pep.2012.10.008. Epub 2012 Nov 7.
6
Recombinant production of antimicrobial peptides in Escherichia coli: a review.大肠杆菌中抗菌肽的重组生产:综述
Protein Expr Purif. 2011 Dec;80(2):260-7. doi: 10.1016/j.pep.2011.08.001. Epub 2011 Aug 6.
7
Production of Nα-acetylated thymosin α1 in Escherichia coli.在大肠杆菌中生产 Nα-乙酰化胸腺肽 α1。
Microb Cell Fact. 2011 Apr 22;10:26. doi: 10.1186/1475-2859-10-26.
8
Recombinant antimicrobial peptide hPAB-β expressed in Pichia pastoris, a potential agent active against methicillin-resistant Staphylococcus aureus.毕赤酵母表达的重组抗菌肽 hPAB-β,一种抗耐甲氧西林金黄色葡萄球菌的潜在有效药物。
Appl Microbiol Biotechnol. 2011 Jan;89(2):281-91. doi: 10.1007/s00253-010-2864-0. Epub 2010 Sep 21.
9
SUMO mediating fusion expression of antimicrobial peptide CM4 from two joined genes in Escherichia coli.SUMO 介导的两串联基因在大肠杆菌中表达抗菌肽 CM4 的融合。
Curr Microbiol. 2011 Jan;62(1):296-300. doi: 10.1007/s00284-010-9705-3. Epub 2010 Jul 17.
10
Development of a Bacillus subtilis expression system using the improved Pglv promoter.利用改良的 Pglv 启动子开发枯草芽孢杆菌表达系统。
Microb Cell Fact. 2010 Jul 10;9:55. doi: 10.1186/1475-2859-9-55.