• 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

三种黄杆菌属物种代谢环烷烃能力的比较研究。

Comparative study of the ability of three xanthobacter species to metabolize cycloalkanes.

机构信息

Department of Life Sciences, Trent Polytechnic, Clifton, Nottingham NG11 8NS, England.

出版信息

Appl Environ Microbiol. 1986 Oct;52(4):665-71. doi: 10.1128/aem.52.4.665-671.1986.

DOI:10.1128/aem.52.4.665-671.1986
PMID:16347162
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC239094/
Abstract

The ability of three species of Xanthobacter to metabolize cyclohexane and its derivatives has been compared. Xanthobacter flavus was unable to utilize any of the cycloalkanes under investigation. X. autotrophicus was unable to utilize cyclohexane but was able to grow with a limited range of substituted cycloalkanes, including cyclohexanol and cyclohexanone. Comparison of a previously isolated cyclohexane growing Xanthobacter sp. with X. flavus and X. autotrophicus indicated it to be closely related to X. autotrophicus. Studies with cell-free extracts have indicated that the route of metabolism for cyclohexanol by X. autotrophicus is the same as that shown for the cyclohexane growing Xanthobacter sp., proceeding via cyclohexanol-->cyclohexanone--> epsilon-caprolactone-->--> adipic acid. A comparison of the cyclohexanol dehydrogenase found in X. autotrophicus with that found in the cyclohexane-growing Xanthobacter sp. indicated these enzymes to be distinctly different from one another on the basis of substrate specificity, molecular weight, and pH optima. The cyclohexanone monooxygenase enzymes found in the two bacteria were also found to be different when the pH optima and cofactor specificity of the two enzymes were compared. Preliminary genetic studies on the cyclohexane-growing Xanthobacter sp. have indicated that there are no plasmids present in this bacterium. The presence of RP4 in the Xanthobacter sp. can be detected following its conjugation with an RP4-carrying Escherichia coli strain.

摘要

比较了三种黄杆菌属物种代谢环己烷及其衍生物的能力。黄杆菌属(Xanthobacter)flavus 无法利用研究中调查的任何环烷烃。X. autotrophicus 无法利用环己烷,但能够在有限的取代环烷烃范围内生长,包括环己醇和环己酮。与先前分离的能够利用环己烷的黄杆菌属(Xanthobacter)sp. 与 X. flavus 和 X. autotrophicus 的比较表明,它与 X. autotrophicus 密切相关。细胞提取物的研究表明,X. autotrophicus 代谢环己醇的途径与能够利用环己烷的黄杆菌属(Xanthobacter)sp. 相同,途径为环己醇→环己酮→ε-己内酯→→己二酸。对 X. autotrophicus 中发现的环己醇脱氢酶与能够利用环己烷的黄杆菌属(Xanthobacter)sp. 中发现的环己醇脱氢酶进行比较,根据底物特异性、分子量和最适 pH 值,表明这些酶彼此明显不同。比较两种细菌中发现的环己酮单加氧酶,当比较两种酶的最适 pH 值和辅因子特异性时,发现它们也不同。对能够利用环己烷的黄杆菌属(Xanthobacter)sp. 的初步遗传研究表明,该细菌中不存在质粒。黄杆菌属(Xanthobacter)sp. 中存在 RP4 可以通过其与携带 RP4 的大肠杆菌菌株的共轭来检测到。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef8f/239094/332642a33965/aem00133-0076-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef8f/239094/14c35fac06a4/aem00133-0075-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef8f/239094/332642a33965/aem00133-0076-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef8f/239094/14c35fac06a4/aem00133-0075-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef8f/239094/332642a33965/aem00133-0076-a.jpg

相似文献

1
Comparative study of the ability of three xanthobacter species to metabolize cycloalkanes.三种黄杆菌属物种代谢环烷烃能力的比较研究。
Appl Environ Microbiol. 1986 Oct;52(4):665-71. doi: 10.1128/aem.52.4.665-671.1986.
2
Isolation and Characterization of a Cyclohexane-Metabolizing Xanthobacter sp.环己烷降解菌黄杆菌的分离与鉴定
Appl Environ Microbiol. 1985 May;49(5):1282-9. doi: 10.1128/aem.49.5.1282-1289.1985.
3
Denitrifying activity of Xanthobacter autotrophicus strains isolated from a submerged fixed-film reactor.从淹没式固定膜反应器中分离出的自养黄色杆菌菌株的反硝化活性。
Appl Microbiol Biotechnol. 2005 Sep;68(5):680-5. doi: 10.1007/s00253-005-1937-y. Epub 2005 Oct 26.
4
A New Catabolic Plasmid in Xanthobacter and Starkeya spp. from a 1,2-Dichloroethane-Contaminated Site.来自1,2-二氯乙烷污染场地的黄杆菌属和斯塔基氏菌属中的一种新的分解代谢质粒
Appl Environ Microbiol. 2016 Aug 15;82(17):5298-308. doi: 10.1128/AEM.01373-16. Print 2016 Sep 1.
5
Genetic organization of the dhlA gene encoding 1,2-dichloroethane dechlorinase from Xanthobacter flavus UE15.来自黄杆菌UE15的编码1,2-二氯乙烷脱氯酶的dhlA基因的遗传组织。
J Microbiol. 2004 Sep;42(3):188-93.
6
Nonconventional hydrolytic dehalogenation of 1-chlorobutane by dehydrated bacteria in a continuous solid-gas biofilter.在连续式固体-气体生物滤池中,脱水细菌对1-氯丁烷进行非传统水解脱卤作用。
Biotechnol Bioeng. 2005 Aug 5;91(3):304-13. doi: 10.1002/bit.20437.
7
Degradation of halogenated aliphatic compounds by Xanthobacter autotrophicus GJ10.自养黄色杆菌GJ10对卤代脂肪族化合物的降解作用
Appl Environ Microbiol. 1985 Mar;49(3):673-7. doi: 10.1128/aem.49.3.673-677.1985.
8
Genetic analysis of pigment biosynthesis in Xanthobacter autotrophicus Py2 using a new, highly efficient transposon mutagenesis system that is functional in a wide variety of bacteria.利用一种新型的、高效的转座子诱变系统对自养黄色杆菌Py2中的色素生物合成进行遗传分析,该系统在多种细菌中均有功能。
Arch Microbiol. 2002 Sep;178(3):193-201. doi: 10.1007/s00203-002-0442-2. Epub 2002 Jun 18.
9
Complete detoxification of tris(2-chloroethyl) phosphate by two bacterial strains: Sphingobium sp. strain TCM1 and Xanthobacter autotrophicus strain GJ10.两株细菌(鞘氨醇单胞菌 TCM1 菌株和黄单胞菌 GJ10 菌株)完全降解三(2-氯乙基)磷酸酯。
J Biosci Bioeng. 2012 Sep;114(3):306-11. doi: 10.1016/j.jbiosc.2012.04.010. Epub 2012 May 10.
10
Shotgun proteomics of Xanthobacter autotrophicus Py2 reveals proteins specific to growth on propylene.黄单胞菌 Py2 的 shotgun 蛋白质组学研究揭示了丙烯生长特异性蛋白。
Arch Microbiol. 2010 Nov;192(11):945-57. doi: 10.1007/s00203-010-0623-3. Epub 2010 Sep 16.

引用本文的文献

1
XanthoMoClo─A Robust Modular Cloning Genetic Toolkit for the Genera and .黄单胞菌-莫拉菌克隆工具包——一种用于黄单胞菌属和莫拉菌属的强大模块化克隆遗传工具包
ACS Synth Biol. 2025 Apr 18;14(4):1173-1190. doi: 10.1021/acssynbio.4c00806. Epub 2025 Mar 13.
2
Degradation of hexane and other recalcitrant hydrocarbons by a novel isolate, Rhodococcus sp. EH831.新型分离菌 Rhodococcus sp. EH831 对己烷和其他难降解烃类的降解。
Environ Sci Pollut Res Int. 2010 Jan;17(1):64-77. doi: 10.1007/s11356-009-0238-x.
3
Simultaneous identification of two cyclohexanone oxidation genes from an environmental Brevibacterium isolate using mRNA differential display.

本文引用的文献

1
Alcohol Dehydrogenase in Drosophila melanogaster: Isozymes and Genetic Variants.果蝇中的醇脱氢酶:同工酶和遗传变异。
Science. 1965 Jul 2;149(3679):80-2. doi: 10.1126/science.149.3679.80.
2
Isolation and Characterization of a Cyclohexane-Metabolizing Xanthobacter sp.环己烷降解菌黄杆菌的分离与鉴定
Appl Environ Microbiol. 1985 May;49(5):1282-9. doi: 10.1128/aem.49.5.1282-1289.1985.
3
Rapid procedure for detection and isolation of large and small plasmids.用于检测和分离大小质粒的快速方法。
利用mRNA差异显示技术从环境短杆菌分离株中同时鉴定两个环己酮氧化基因。
J Bacteriol. 2000 Aug;182(15):4241-8. doi: 10.1128/JB.182.15.4241-4248.2000.
4
Biodegradation of cyclohexylamine by Brevibacterium oxydans IH-35A.氧化短杆菌IH-35A对环己胺的生物降解作用。
Appl Environ Microbiol. 1999 May;65(5):2232-4. doi: 10.1128/AEM.65.5.2232-2234.1999.
J Bacteriol. 1981 Mar;145(3):1365-73. doi: 10.1128/jb.145.3.1365-1373.1981.
4
Rapid methods for the study of both stable and unstable plasmids in Pseudomonas.研究假单胞菌中稳定和不稳定质粒的快速方法。
J Gen Microbiol. 1981 Jun;124(2):433-7. doi: 10.1099/00221287-124-2-433.
5
A rapid boiling method for the preparation of bacterial plasmids.一种制备细菌质粒的快速煮沸法。
Anal Biochem. 1981 Jun;114(1):193-7. doi: 10.1016/0003-2697(81)90473-5.
6
The metabolism of cyclohexanol by Nocardia globerula CL1.球形诺卡氏菌CL1对环己醇的代谢
Biochem J. 1971 Feb;121(3):363-70. doi: 10.1042/bj1210363.
7
Molecular nature of two nonconjugative plasmids carrying drug resistance genes.携带耐药基因的两种非接合质粒的分子特性
J Bacteriol. 1974 Feb;117(2):619-30. doi: 10.1128/jb.117.2.619-630.1974.
8
A rapid method for the identification of plasmid desoxyribonucleic acid in bacteria.一种鉴定细菌中质粒脱氧核糖核酸的快速方法。
Plasmid. 1978 Sep;1(4):584-8. doi: 10.1016/0147-619x(78)90016-1.
9
Isolation of large bacterial plasmids and characterization of the P2 incompatibility group plasmids pMG1 and pMG5.大型细菌质粒的分离及P2不相容群质粒pMG1和pMG5的特性分析
J Bacteriol. 1978 Jul;135(1):227-38. doi: 10.1128/jb.135.1.227-238.1978.