• 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

相似文献

1
Amino acid substitutions at Ambler position Gly238 in the SHV-1 beta-lactamase: exploring sequence requirements for resistance to penicillins and cephalosporins.SHV-1β-内酰胺酶中安布勒位置Gly238处的氨基酸取代:探索对青霉素和头孢菌素耐药性的序列要求。
Antimicrob Agents Chemother. 2002 Dec;46(12):3971-7. doi: 10.1128/AAC.46.12.3971-3977.2002.
2
Construction and characterization of mutants of the TEM-1 beta-lactamase containing amino acid substitutions associated with both extended-spectrum resistance and resistance to beta-lactamase inhibitors.构建并鉴定含有与超广谱耐药性和对β-内酰胺酶抑制剂耐药性相关氨基酸取代的TEM-1β-内酰胺酶突变体。
Antimicrob Agents Chemother. 1999 Aug;43(8):1881-7. doi: 10.1128/AAC.43.8.1881.
3
Role of Asp104 in the SHV beta-lactamase.天冬氨酸104在超广谱β-内酰胺酶中的作用。
Antimicrob Agents Chemother. 2006 Dec;50(12):4124-31. doi: 10.1128/AAC.00848-06. Epub 2006 Sep 18.
4
Mutagenesis of amino acid residues in the SHV-1 beta-lactamase: the premier role of Gly238Ser in penicillin and cephalosporin resistance.SHV-1β-内酰胺酶中氨基酸残基的诱变:Gly238Ser在对青霉素和头孢菌素耐药性中的首要作用。
Biochim Biophys Acta. 2001 May 5;1547(1):37-50. doi: 10.1016/s0167-4838(01)00164-9.
5
Molecular genetics of resistance to both ceftazidime and beta-lactam-beta-lactamase inhibitor combinations in Klebsiella pneumoniae and in vivo response to beta-lactam therapy.肺炎克雷伯菌对头孢他啶和β-内酰胺-β-内酰胺酶抑制剂联合用药的耐药分子遗传学及对β-内酰胺治疗的体内反应
J Infect Dis. 1996 Jan;173(1):151-8. doi: 10.1093/infdis/173.1.151.
6
Aspartic acid for asparagine substitution at position 276 reduces susceptibility to mechanism-based inhibitors in SHV-1 and SHV-5 beta-lactamases.天冬氨酸替代276位的天冬酰胺会降低SHV-1和SHV-5β-内酰胺酶对基于机制的抑制剂的敏感性。
J Antimicrob Chemother. 1999 Jan;43(1):23-9. doi: 10.1093/jac/43.1.23.
7
OHIO-1 beta-lactamase mutants: Asp179Gly mutation confers resistance to ceftazidime.俄亥俄-1β-内酰胺酶突变体:天冬氨酸179突变为甘氨酸的突变使细菌对头孢他啶产生耐药性。
FEMS Microbiol Lett. 1997 Jul 15;152(2):275-8. doi: 10.1111/j.1574-6968.1997.tb10439.x.
8
Activity of ceftazidime/avibactam against isogenic strains of Escherichia coli containing KPC and SHV β-lactamases with single amino acid substitutions in the Ω-loop.头孢他啶/阿维巴坦对含KPC和SHVβ-内酰胺酶且Ω环有单个氨基酸取代的大肠杆菌同基因菌株的活性。
J Antimicrob Chemother. 2015 Aug;70(8):2279-86. doi: 10.1093/jac/dkv094. Epub 2015 May 8.
9
Role of Ser-238 and Lys-240 in the hydrolysis of third-generation cephalosporins by SHV-type beta-lactamases probed by site-directed mutagenesis and three-dimensional modeling.通过定点诱变和三维建模探究Ser-238和Lys-240在SHV型β-内酰胺酶水解第三代头孢菌素中的作用
J Biol Chem. 1993 Feb 15;268(5):3690-7.
10
Evaluation of the NCCLS extended-spectrum beta-lactamase confirmation methods for Escherichia coli with isolates collected during Project ICARE.对在关爱项目期间收集的大肠杆菌分离株,采用美国国家临床实验室标准委员会(NCCLS)超广谱β-内酰胺酶确证方法进行评估。
J Clin Microbiol. 2003 Jul;41(7):3142-6. doi: 10.1128/JCM.41.7.3142-3146.2003.

引用本文的文献

1
Allogenous Selection of Mutational Collateral Resistance: Old Drugs Select for New Resistance Within Antibiotic Families.突变性间接耐药的同种异体选择:旧药物在抗生素家族中选择新的耐药性。
Front Microbiol. 2021 Oct 22;12:757833. doi: 10.3389/fmicb.2021.757833. eCollection 2021.
2
Predicting β-lactam resistance using whole genome sequencing in Klebsiella pneumoniae: the challenge of β-lactamase inhibitors.使用全基因组测序预测肺炎克雷伯菌中的β-内酰胺类药物耐药性:β-内酰胺酶抑制剂的挑战。
Diagn Microbiol Infect Dis. 2020 Nov;98(3):115149. doi: 10.1016/j.diagmicrobio.2020.115149. Epub 2020 Jul 25.
3
Bioassay Guided Isolation and Docking Studies of a Potential β-Lactamase Inhibitor from .生物测定指导的从. 中分离和对接研究一种有潜力的β-内酰胺酶抑制剂
Molecules. 2020 May 31;25(11):2566. doi: 10.3390/molecules25112566.
4
Beyond Piperacillin-Tazobactam: Cefepime and AAI101 as a Potent β-Lactam-β-Lactamase Inhibitor Combination.超越哌拉西林他唑巴坦:头孢吡肟和 AAI101 作为一种强效的β-内酰胺-β-内酰胺酶抑制剂组合。
Antimicrob Agents Chemother. 2019 Apr 25;63(5). doi: 10.1128/AAC.00105-19. Print 2019 May.
5
Direct detection of extended-spectrum beta-lactamases (CTX-M) from blood cultures by LC-MS/MS bottom-up proteomics.LC-MS/MS 下法蛋白质组学直接检测血培养中的超广谱β-内酰胺酶(CTX-M)。
Eur J Clin Microbiol Infect Dis. 2017 Sep;36(9):1621-1628. doi: 10.1007/s10096-017-2975-y. Epub 2017 Apr 10.
6
Editorial Commentary: Ceftazidime-Avibactam and Carbapenem-Resistant Enterobacteriaceae: "We're Gonna Need a Bigger Boat".编辑评论:头孢他啶-阿维巴坦与耐碳青霉烯类肠杆菌科细菌:“我们需要一艘更大的船” 。 (注:这里“We're Gonna Need a Bigger Boat”出自电影《大白鲨》,意译在此处表示应对这类细菌感染可能需要更有效的手段等含义 )
Clin Infect Dis. 2016 Dec 15;63(12):1619-1621. doi: 10.1093/cid/ciw639. Epub 2016 Sep 13.
7
Click Chemistry in Lead Optimization of Boronic Acids as β-Lactamase Inhibitors.点击化学在硼烷作为β-内酰胺酶抑制剂的先导优化中的应用。
J Med Chem. 2015 Jul 23;58(14):5445-58. doi: 10.1021/acs.jmedchem.5b00341. Epub 2015 Jul 10.
8
Activities of ceftazidime, ceftaroline, and aztreonam alone and combined with avibactam against isogenic Escherichia coli strains expressing selected single β-lactamases.头孢他啶、头孢洛林和氨曲南单独及与阿维巴坦联合使用对表达选定单一β-内酰胺酶的同基因大肠杆菌菌株的活性。
Diagn Microbiol Infect Dis. 2015 May;82(1):65-9. doi: 10.1016/j.diagmicrobio.2015.02.003. Epub 2015 Feb 14.
9
Effect of asparagine substitutions in the YXN loop of a class C β-lactamase of Acinetobacter baumannii on substrate and inhibitor kinetics.鲍曼不动杆菌C类β-内酰胺酶YXN环中天冬酰胺替换对底物和抑制剂动力学的影响。
Antimicrob Agents Chemother. 2015 Mar;59(3):1472-7. doi: 10.1128/AAC.03537-14. Epub 2014 Dec 22.
10
Can inhibitor-resistant substitutions in the Mycobacterium tuberculosis β-Lactamase BlaC lead to clavulanate resistance?: a biochemical rationale for the use of β-lactam-β-lactamase inhibitor combinations.结核分枝杆菌β-内酰胺酶BlaC中的抑制剂抗性取代会导致克拉维酸耐药吗?:使用β-内酰胺-β-内酰胺酶抑制剂组合的生化原理。
Antimicrob Agents Chemother. 2013 Dec;57(12):6085-96. doi: 10.1128/AAC.01253-13. Epub 2013 Sep 23.

本文引用的文献

1
Development of a sensitive and specific enzyme-linked immunosorbent assay for detecting and quantifying CMY-2 and SHV beta-lactamases.用于检测和定量CMY-2和SHVβ-内酰胺酶的灵敏且特异的酶联免疫吸附测定法的开发。
J Clin Microbiol. 2002 Jun;40(6):1947-57. doi: 10.1128/JCM.40.6.1947-1957.2002.
2
Rapid method of extraction and analysis of extended-spectrum beta-lactamases from clinical strains of Klebsiella pneumoniae.从肺炎克雷伯菌临床菌株中快速提取和分析超广谱β-内酰胺酶的方法
Clin Microbiol Infect. 2001 Dec;7(12):709-11.
3
Mutagenesis of amino acid residues in the SHV-1 beta-lactamase: the premier role of Gly238Ser in penicillin and cephalosporin resistance.SHV-1β-内酰胺酶中氨基酸残基的诱变:Gly238Ser在对青霉素和头孢菌素耐药性中的首要作用。
Biochim Biophys Acta. 2001 May 5;1547(1):37-50. doi: 10.1016/s0167-4838(01)00164-9.
4
Predicting the emergence of antibiotic resistance by directed evolution and structural analysis.通过定向进化和结构分析预测抗生素耐药性的出现。
Nat Struct Biol. 2001 Mar;8(3):238-42. doi: 10.1038/84981.
5
Characterization of the extended-spectrum beta-lactamase reference strain, Klebsiella pneumoniae K6 (ATCC 700603), which produces the novel enzyme SHV-18.产新型酶SHV-18的超广谱β-内酰胺酶参考菌株肺炎克雷伯菌K6(ATCC 700603)的特性分析
Antimicrob Agents Chemother. 2000 Sep;44(9):2382-8. doi: 10.1128/AAC.44.9.2382-2388.2000.
6
SHV-13, a novel extended-spectrum beta-lactamase, in Klebsiella pneumoniae isolates from patients in an intensive care unit in Amsterdam.SHV-13,一种新型超广谱β-内酰胺酶,存在于阿姆斯特丹一家重症监护病房患者分离出的肺炎克雷伯菌中。
Antimicrob Agents Chemother. 2000 Apr;44(4):1081-4. doi: 10.1128/AAC.44.4.1081-1084.2000.
7
High-level expression of chromosomally encoded SHV-1 beta-lactamase and an outer membrane protein change confer resistance to ceftazidime and piperacillin-tazobactam in a clinical isolate of Klebsiella pneumoniae.染色体编码的SHV-1β-内酰胺酶的高表达和外膜蛋白变化赋予肺炎克雷伯菌临床分离株对头孢他啶和哌拉西林-他唑巴坦的耐药性。
Antimicrob Agents Chemother. 2000 Feb;44(2):362-7. doi: 10.1128/AAC.44.2.362-367.2000.
8
Structure of the SHV-1 beta-lactamase.SHV-1β-内酰胺酶的结构。
Biochemistry. 1999 May 4;38(18):5720-7. doi: 10.1021/bi990136d.
9
The role of residue 238 of TEM-1 beta-lactamase in the hydrolysis of extended-spectrum antibiotics.TEM-1β-内酰胺酶238位残基在超广谱抗生素水解中的作用。
J Biol Chem. 1998 Oct 9;273(41):26603-9. doi: 10.1074/jbc.273.41.26603.
10
Kinetic analysis of an inhibitor-resistant variant of the OHIO-1 beta-lactamase, an SHV-family class A enzyme.SHV家族A类酶OHIO-1β-内酰胺酶的一种抑制剂抗性变体的动力学分析。
Biochem J. 1998 Jul 15;333 ( Pt 2)(Pt 2):395-400. doi: 10.1042/bj3330395.

SHV-1β-内酰胺酶中安布勒位置Gly238处的氨基酸取代:探索对青霉素和头孢菌素耐药性的序列要求。

Amino acid substitutions at Ambler position Gly238 in the SHV-1 beta-lactamase: exploring sequence requirements for resistance to penicillins and cephalosporins.

作者信息

Hujer Andrea M, Hujer Kristine M, Helfand Marion S, Anderson Vernon E, Bonomo Robert A

机构信息

Research Service. Infectious Diseases Service, Louis Stokes Cleveland Department of Veterans Affairs Medical Center, Ohio 44106, USA.

出版信息

Antimicrob Agents Chemother. 2002 Dec;46(12):3971-7. doi: 10.1128/AAC.46.12.3971-3977.2002.

DOI:10.1128/AAC.46.12.3971-3977.2002
PMID:12435703
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC132793/
Abstract

Site saturation mutagenesis of the 238 position in the SHV beta-lactamase was performed to identify the complete sequence requirements needed for the extended spectrum beta-lactamase (ESBL) phenotype. MICs (in micrograms per milliliter) in an isogenic background, Escherichia coli DH10B, demonstrated that the Gly238Ala mutation conferred the most resistance to penicillins and cephalosporins. The absolute increase in resistance was greatest against cefotaxime for the Gly238Ala mutant (0.06 to 8 micro g/ml). Except for the strain possessing the Gly238Pro beta-lactamase, ceftazidime MICs were also elevated. None of the mutant SHV beta-lactamases were expressed in as great an amount as the wild-type beta-lactamase. Kinetic analysis of the Gly238Ala mutant revealed that penicillin and cephalosporin substrates have a lower K(m) for the enzyme because of this mutation. Ampicillin and piperacillin MICs were inversely proportional to the side chain volume of the amino acid in cases larger than Ser, suggesting that steric considerations may be a primary requirement for penicillin resistance. Secondary structural effects explain increased resistance to oxyiminocephalosporins. Based upon this study, we anticipate that additional mutations of Gly238 in the SHV beta-lactamase will continue to be discovered with an ESBL (ceftazidime or cefotaxime resistant) phenotype.

摘要

对超广谱β-内酰胺酶(ESBL)表型所需的完整序列要求进行了研究,对SHVβ-内酰胺酶238位进行了位点饱和诱变。在同基因背景的大肠杆菌DH10B中,最低抑菌浓度(以微克/毫升计)表明,Gly238Ala突变对青霉素和头孢菌素的耐药性最强。Gly238Ala突变体对头孢噻肟的耐药性绝对增加最大(从0.06到8微克/毫升)。除了具有Gly238Proβ-内酰胺酶的菌株外,头孢他啶的最低抑菌浓度也有所升高。突变的SHVβ-内酰胺酶表达量均不如野生型β-内酰胺酶高。对Gly238Ala突变体的动力学分析表明,由于该突变,青霉素和头孢菌素底物对该酶的米氏常数(K(m))较低。在氨基酸侧链体积大于丝氨酸的情况下,氨苄西林和哌拉西林的最低抑菌浓度与氨基酸侧链体积成反比,这表明空间因素可能是青霉素耐药性的主要要求。二级结构效应解释了对氧亚氨基头孢菌素耐药性的增加。基于这项研究,我们预计在SHVβ-内酰胺酶中Gly238的其他突变将继续被发现具有ESBL(对头孢他啶或头孢噻肟耐药)表型。