EN
登录

黄曲霉素A的抗菌作用及作用机制研究

Antibacterial and mechanism of action studies of boxazomycin A

Nature 等信源发布 2024-08-01 15:18

可切换为仅中文


AbstractBoxazomycins A-C are potent broad-spectrum antibiotics isolated from Actinomycetes strain G495-1 in 1987. We now report that boxazomycin A inhibits bacterial growth by selectively inhibiting protein synthesis, its effect is bacteriostatic, and it is equally active against drug resistant bacterial strains.

摘要Boxazomycins A-C是1987年从放线菌G495-1菌株中分离出的有效广谱抗生素。我们现在报道,boxazomycin A通过选择性抑制蛋白质合成来抑制细菌生长,其作用是抑菌的,并且对耐药菌株具有同等活性。

No cross-resistance to protein synthesis inhibitors was observed suggesting that its inhibition is distinct from clinical protein synthesis inhibitors. We also report in vivo efficacy in a Staphylococcus aureus murine infection model supported by corresponding pharmacokinetic studies..

未观察到对蛋白质合成抑制剂的交叉耐药性,表明其抑制作用不同于临床蛋白质合成抑制剂。我们还报告了相应的药代动力学研究支持的金黄色葡萄球菌鼠感染模型的体内疗效。。

Access through your institution

通过您的机构访问

Buy or subscribe

购买或订阅

This is a preview of subscription content, access via your institution

这是订阅内容的预览,可通过您的机构访问

Access options

Access through your institution

通过您的机构访问

Access through your institution

通过您的机构访问

Change institution

变革机构

Buy or subscribe

购买或订阅

Subscribe to this journalReceive 12 print issues and online access251,40 € per yearonly 20,95 € per issueLearn moreBuy this articlePurchase on Springer LinkInstant access to full article PDFBuy nowPrices may be subject to local taxes which are calculated during checkout

订阅本期刊每年可收到12期印刷版和在线访问251,40欧元每期仅20,95欧元了解更多购买本文在Springer Link上购买即时访问全文PDFBuy NOW价格可能需要缴纳结帐时计算的当地税费

Additional access options:

其他访问选项:

Log in

登录

Learn about institutional subscriptions

了解机构订阅

Read our FAQs

阅读我们的常见问题

Contact customer support

联系客户支持

Fig. 1Fig. 2Fig. 3Fig. 4Fig. 5

图1图。图2。3图。。5

ReferencesSingh SB, Phillips JW, Wang J. Highly, sensitive target based whole cell antibacterial discovery strategy by antisense RNA silencing. Curr Opin Drug Discov Dev. 2007;10:160.CAS

Referencessing SB,Phillips JW,Wang J.通过反义RNA沉默的高度敏感的基于靶标的全细胞抗菌发现策略。Curr Opin Drug Discov Dev.2007;10: 160.CAS

Google Scholar

谷歌学者

Zhang C, Occi J, Masurekar P, Barrett JF, Zink DL, Smith S, Onishi R, Ha S, Salazar O, Genilloud O, Basilio A, Vicente F, Gill C, Hickey EJ, Dorso K, Motyl M, Singh SB. Isolation, structure, and antibacterial activity of philipimycin, a thiazolyl peptide discovered from Actinoplanes philippinensis MA7347.

Zhang C,Occi J,Masurekar P,Barrett JF,Zink DL,Smith S,Onishi R,Ha S,Salazar O,Genilloud O,Basilio A,Vicente F,Gill C,Hickey EJ,Dorso K,Motyl M,Singh SB。从菲律宾放线菌MA7347中发现的噻唑基肽菲利普霉素的分离,结构和抗菌活性。

J Am Chem Soc. 2008;130:12102.Article .

J Am Chem Soc。2008;130:12102。文章。

CAS

中科院

PubMed

PubMed

Google Scholar

谷歌学者

Wang J, Soisson SM, Young K, Shoop W, Kodali S, Galgoci A, Painter R, Parthasarathy G, Tang Y, Cummings R, Ha S, Dorso K, Motyl M, Jayasuriya H, Ondeyka J, Herath K, Zhang C, Hernandez L, Alloco J, Basilio Á, Tormo JR, Genilloud O, Vicente F, Pelaez F, Colwell L, Lee SH, Michael B, Felcetto T, Gill C, Silver LL, Hermes J, Bartizal K, Barrett J, Schmatz D, Becker JW, Cully D, Singh SB.

王J,索伊松SM,杨K,肖普W,科达利S,加尔戈奇A,画家R,帕塔萨拉西G,唐Y,卡明斯R,哈S,多尔索K,莫蒂尔M,贾亚苏里亚H,Ondeyka J,赫拉思K,张C,埃尔南德斯L,阿洛科J,巴西利奥Á,托莫JR,吉诺德O,维森特F,佩莱兹F,科尔维尔L,李SH,迈克尔B,费尔塞托T,吉尔C,西尔弗LL,赫尔墨斯J,巴蒂扎尔K,巴雷特J,施马茨D,贝克尔JW,卡利D,辛格SB。

Platensimycin is a selective FabF inhibitor with potent antibiotic properties. Nature. 2006;441:358.Article .

铂霉素是一种选择性FabF抑制剂,具有有效的抗生素特性。自然。2006年;441:358。条款。

CAS

中科院

PubMed

PubMed

Google Scholar

谷歌学者

Singh SB, Jayasuriya H, Ondeyka JG, Herath KB, Zhang C, Zink DL, Tsou NN, Ball RG, Basilio A, Genilloud O, Diez MT, Vicente F, Pelaez F, Young K, Wang J. Isolation, structure, and absolute stereochemistry of platensimycin, a broad spectrum antibiotic discovered using an antisense differential sensitivity strategy.

Singh SB,Jayasuriya H,Ondeyka JG,Herath KB,Zhang C,Zink DL,Tsou NN,Ball RG,Basilio A,Genilloud O,Diez MT,Vicente F,Pelaez F,Young K,Wang J.分离,结构和绝对立体化学。铂霉素是一种使用反义差异敏感性策略发现的广谱抗生素。

J Am Chem Soc. 2006;128:11916.Article .

J Am Chem Soc。2006;128:11916。条款。

CAS

中科院

PubMed

PubMed

Google Scholar

谷歌学者

Jayasuriya H, Herath KB, Zhang C, Zink DL, Basilio A, Genilloud O, Diez MT, Vicente F, Gonzalez I, Salazar O, Pelaez F, Cummings R, Ha S, Wang J, Singh SB. Isolation and structure of platencin: a novel FabH and FabF dual inhibitor with potent broad spectrum antibiotic activity produced by Streptomyces platensis MA7339.

Jayasuriya H,Herath KB,Zhang C,Zink DL,Basilio A,Genilloud O,Diez MT,Vicente F,Gonzalez I,Salazar O,Pelaez F,Cummings R,Ha S,Wang J,Singh SB。血小板素的分离和结构:一种新型FabH和FabF双重抑制剂,具有由链霉菌(Streptomyces platensis)MA7339产生的强效广谱抗生素活性。

Angew Chem Int Ed. 2007;46:4684.Article .

Angew Chem Int Ed.2007;46:4684。第条。

CAS

中科院

Google Scholar

谷歌学者

Wang J, Kodali S, Lee SH, Galgoci A, Painter R, Dorso K, Racine F, Motyl M, Hernandez L, Tinney E, Colletti S, Herath K, Cummings R, Salazar O, Gonzalez I, Basilio A, Vicente F, Genilloud O, Pelaez F, Jayasuriya H, Young K, Cully D, Singh SB. Platencin is a dual FabF and FabH inhibitor with potent in vivo antibiotic properties.

Wang J,Kodali S,Lee SH,Galgoci A,Painter R,Dorso K,Racine F,Motyl M,Hernandez L,Tinney E,Colletti S,Herath K,Cummings R,Salazar O,Gonzalez I,Basilio A,Vicente F,Genilloud O,Pelaez F,Jayasuriya H,Young K,Cully D,Singh SB。Platencin是一种双重FabF和FabH抑制剂,具有有效的体内抗生素特性。

Proc Natl Acad Sci (USA). 2007;104:7612.Article .

Proc Natl Acad Sci (USA). 2007;104:7612.Article .

CAS

中科院

PubMed

PubMed

Google Scholar

谷歌学者

Phillips JW, Goetz MA, Smith SK, Zink DL, Polishook J, Onishi R, Salowe S, Wiltsie J, Allocco J, Sigmund J, Dorso K, Lee S, Skwish S, de la Cruz M, Martin J, Vicente F, Genilloud O, Lu J, Painter RE, Young K, Overbye K, Donald RG, Singh SB. Discovery of kibdelomycin, a potent new class of bacterial type II topoisomerase inhibitor by chemical-genetic profiling in Staphylococcus aureus.

Phillips JW,Goetz MA,Smith SK,Zink DL,Polishook J,Onishi R,Salowe S,Wiltsie J,Allocco J,Sigmund J,Dorso K,Lee S,Skwish S,de la Cruz M,Martin J,Vicente F,Genilloud O,Lu J,Painter RE,Young K,Overbye K,Donald RG,Singh SB。通过金黄色葡萄球菌的化学遗传分析发现了kibdelomycin,一种有效的新型细菌II型拓扑异构酶抑制剂。

Chem Biol. 2011;18:955.Article .

化学生物学。2011;18:955.条款[联合王国]。

CAS

中科院

PubMed

PubMed

Google Scholar

谷歌学者

Singh SB, Goetz MA, Smith SK, Zink DL, Polishook J, Onishi R, Salowe S, Wiltsie J, Allocco J, Sigmund J, Dorso K, de la Cruz M, Martin J, Vicente F, Genilloud O, Donald RG, Phillips JW. Kibdelomycin A, a congener of kibdelomycin, derivatives and their antibacterial activities. Bioorg Med Chem Lett.

辛格SB,戈茨MA,史密斯SK,津克DL,波利胡克J,奥尼希R,萨洛维S,威尔西J,阿洛科J,西格蒙德J,多尔索K,德拉克鲁斯M,马丁J,维森特F,吉尼洛德O,唐纳德RG,菲利普斯JW。Kibdelomycin A是Kibdelomycin的同系物,其衍生物及其抗菌活性。Bioorg Med Chem Lett。

2012;22:7127.Article .

2012年;22:7127。文章。

CAS

中科院

PubMed

PubMed

Google Scholar

谷歌学者

Lu J, Patel S, Sharma N, Soisson SM, Kishii R, Takei M, Fukuda Y, Lumb KJ, Singh SB. Structures of kibdelomycin bound to Staphylococcus aureus GyrB and ParE showed a novel U-shaped binding mode. ACS Chem Biol. 2014;9:2023.Article

Lu J,Patel S,Sharma N,Soisson SM,Kishii R,Takei M,Fukuda Y,Lumb KJ,Singh SB。与金黄色葡萄球菌GyrB和ParE结合的kibdelomycin结构显示出新的U形结合模式。ACS化学生物学。2014年;9: 2023年条款

CAS

中科院

PubMed

PubMed

Google Scholar

谷歌学者

Miesel L, Hecht DW, Osmolski JR, Gerding D, Flattery A, Li F, Lan J, Lipari P, Polishook JD, Liang L, Liu J, Olsen DB, Singh SB. Kibdelomycin is a potent and selective agent against toxigenic Clostridium difficile. Antimicrob Agents Chemother. 2014;58:2387.Article

Miesel L,Hecht DW,Osmolski JR,Gerding D,Flattery A,Li F,Lan J,Lipari P,Polishook JD,Liang L,Liu J,Olsen DB,Singh SB。Kibdelomycin是一种有效且选择性的抗产毒性艰难梭菌的药物。抗菌剂Chemother。2014年;58:2387.文章

PubMed

PubMed

PubMed Central

公共医学中心

Google Scholar

谷歌学者

Singh SB, Dayananth P, Balibar CJ, Garlisi CG, Lu J, Kishii R, Takei M, Fukuda Y, Ha S, Young K. Kibdelomycin is a bactericidal broad-spectrum aerobic antibacterial agent. Antimicrob Agents Chemother. 2015;59:3474.Article

。抗菌剂Chemother。2015年;59:3474.文章

CAS

中科院

PubMed

PubMed

PubMed Central

公共医学中心

Google Scholar

谷歌学者

Singh SB. Discovery and development of kibdelomycin, a new class of broad-spectrum antibiotics targeting the clinically proven bacterial type II topoisomerase. Bioorg Med Chem. 2016;24:6291.Article

Singh SB.kibdelomycin的发现和开发,kibdelomycin是一类针对临床证明的细菌II型拓扑异构酶的新型广谱抗生素。Bioorg医学化学。2016年;24:6291.文章

CAS

中科院

PubMed

PubMed

Google Scholar

谷歌学者

Saitoh, K; Konishi, M; Tomita, K, Boxazomycin A and B, new antibiotics containing benzoxazole nucleus, US 4,690,926, 1987.Kusumi T, Ooi T, Walchli MR, Kakisawa H. Structure of the novel antibiotics boxazomycins A, B, and C. J Am Chem Soc. 1988;110:2954.Article

斋藤,K;科尼希,M;Tomita,K,Boxazomycin A和B,含有苯并恶唑核的新抗生素,US 46909261987。Kusumi T,Ooi T,Walchli MR,Kakisawa H.新型抗生素boxazomycins A,B和C的结构。J Am Chem Soc。1988;110:2954.文章

CAS

中科院

Google Scholar

谷歌学者

Suto MJ, Turner WR. Synthesis of Boxazomycin B and related analogs. Tetrahedron Lett. 1995;36:7213.Article

Suto MJ,Turner WR。Boxazomycin B及其类似物的合成。四面体Lett。1995年;36:7213.文章

CAS

中科院

Google Scholar

谷歌学者

Richardson C, Rewcastle GW, Hoyer D, Denny WA. Palladium-catalyzed cross-coupling in the synthesis of pyridinyl boxazomycin C analogues. J Org Chem. 2005;70:7436.Article

理查森C,Rewcastle GW,霍耶D,丹尼WA。。J组织化学。2005年;70:7436.文章

CAS

中科院

PubMed

PubMed

Google Scholar

谷歌学者

Šlachtová V, Brulíková L. Benzoxazole derivatives as promising antitubercular agents. ChemistrySelect. 2018;3:4653.Article

ŠlachtováV,BrulíkováL.苯并恶唑衍生物作为有前景的抗结核药物。化学选择。2018;3:4653文章

Google Scholar

谷歌学者

Singh SB, Occi J, Jayasuriya H, Herath K, Motyl M, Dorso K, Gill C, Hickey E, Overbye KM, Barrett JF, Masurekar P. Antibacterial evaluations of thiazomycin- a potent thiazolyl peptide antibiotic from Amycolatopsis fastidiosa. J Antibiot (Tokyo). 2007;60:565.Article

Singh SB,Occi J,Jayasuriya H,Herath K,Motyl M,Dorso K,Gill C,Hickey E,Overbye KM,Barrett JF,Masurekar P.噻唑霉素的抗菌评估-一种有效的噻唑基肽抗生素,来自Amycolatopsis fastidiosa。J Antibiot(东京)。2007年;60:565.文章

CAS

中科院

PubMed

PubMed

Google Scholar

谷歌学者

Onishi HR, Pelak BA, Gerckens LS, Silver LL, Kahan FM, Chen MH, Patchett AA, Galloway SM, Hyland SA, Anderson MS, Raetz CR. Antibacterial agents that inhibit lipid A biosynthesis. C R Sci. 1996;274:980.CAS

Onishi HR,Pelak BA,Gerckens LS,Silver LL,Kahan FM,Chen MH,Patchett AA,Galloway SM,Hyland SA,Anderson MS,Raetz CR.抑制脂质A生物合成的抗菌剂。C R科学。1996年;274:980.CAS

Google Scholar

谷歌学者

Download referencesAuthor informationAuthor notesSheo B. SinghPresent address: Charles A Dana Research Institute of Scientist Emeriti, Drew University, Madison, NJ, 07054, USASheo B. SinghPresent address: Department of chemistry & Chemical Biology, Stevens Institute of Technology, Hoboken, NJ, 07030, USAJames OcciPresent address: Center for Vector Biology, Rutgers University, New Brunswick, NJ, 08901, USADeceased: John OndeykaDeceased: John F.

下载参考文献作者信息作者注释Sheo B.SinghPresent地址:Charles A Dana Research Institute of Scientist Emeriti,Drew University,Madison,NJ,07054,USASheo B.SinghPresent地址:美国新泽西州霍博肯史蒂文斯理工学院化学与化学生物学系,07030,USAJames Occpresent地址:罗格斯大学矢量生物学中心,新泽西州新不伦瑞克,08901,USA死者:John Ondeykadestopped:John F。

BarrettDeceased: Prakash MasurekarAuthors and AffiliationsMerck & Co. Inc., Rahway, NJ, 07065, USASheo B. Singh, James Occi, John Ondeyka, John F. Barrett, Prakash Masurekar, Mary Motyl, Charles Gill & Gino SalituroAuthorsSheo B. SinghView author publicationsYou can also search for this author in.

巴雷特已故:Prakash MasurekaAuthors and AffiliationsMerck&Co.Inc.,新泽西州拉赫韦,07065,USASheo B.Singh,James Occi,John Ondeyka,John F.Barrett,Prakash Masurekar,Mary Motyl,Charles Gill&Gino Saliturauthoussheo B.SinghView作者出版物您也可以在中搜索这位作者。

PubMed Google ScholarJames OcciView author publicationsYou can also search for this author in

PubMed谷歌学者James OcciView作者出版物您也可以在

PubMed Google ScholarJohn OndeykaView author publicationsYou can also search for this author in

PubMed谷歌学者John OndeykaView作者出版物您也可以在

PubMed Google ScholarJohn F. BarrettView author publicationsYou can also search for this author in

PubMed谷歌学者John F.BarrettView作者出版物您也可以在

PubMed Google ScholarPrakash MasurekarView author publicationsYou can also search for this author in

PubMed Google ScholarPrakash MasurekarView作者出版物您也可以在

PubMed Google ScholarMary MotylView author publicationsYou can also search for this author in

PubMed Google ScholarMary MotylView作者出版物您也可以在

PubMed Google ScholarCharles GillView author publicationsYou can also search for this author in

PubMed Google ScholarCharles GillView作者出版物您也可以在

PubMed Google ScholarGino SalituroView author publicationsYou can also search for this author in

PubMed Google ScholarGino SalituroView作者出版物您也可以在

PubMed Google ScholarCorresponding authorCorrespondence to

PubMed谷歌学者通讯社

Sheo B. Singh.Ethics declarations

谢奥·辛格。道德宣言

Conflict of interest

利益冲突

All authors were employed by Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA where this work was conducted.

所有作者均受雇于Merck Sharp&Dohme LLC,Merck&Co.,Inc.,Rahway,NJ,USA的子公司。

Additional informationPublisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.Rights and permissionsSpringer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.Reprints and permissionsAbout this articleCite this articleSingh, S.B., Occi, J., Ondeyka, J.

Additional informationPublisher的注释Springer Nature在已发布的地图和机构隶属关系中的管辖权主张方面保持中立。权利和许可Pringer Nature或其许可人(例如协会或其他合作伙伴)根据与作者或其他权利持有人的出版协议对本文拥有专有权;本文接受稿件版本的作者自行存档仅受此类出版协议和适用法律的条款管辖。转载和许可本文引用本文Singh,S.B.,Occi,J.,Ondeyka,J。

et al. Antibacterial and mechanism of action studies of boxazomycin A..

boxazomycin A的抗菌作用和作用机制研究。。

J Antibiot (2024). https://doi.org/10.1038/s41429-024-00757-9Download citationReceived: 17 January 2024Revised: 20 April 2024Accepted: 18 June 2024Published: 01 August 2024DOI: https://doi.org/10.1038/s41429-024-00757-9Share this articleAnyone you share the following link with will be able to read this content:Get shareable linkSorry, a shareable link is not currently available for this article.Copy to clipboard.

J Antibiot(2024)。https://doi.org/10.1038/s41429-024-00757-9Download引文收到日期:2024年1月17日修订日期:2024年4月20日接受日期:2024年6月18日发布日期:2024年8月1日OI:https://doi.org/10.1038/s41429-024-00757-9Share本文与您共享以下链接的任何人都可以阅读此内容:获取可共享链接对不起,本文目前没有可共享的链接。复制到剪贴板。

Provided by the Springer Nature SharedIt content-sharing initiative

由Springer Nature SharedIt内容共享计划提供