ASIA unversity:Item 310904400/2482
English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 94286/110023 (86%)
造访人次 : 21656992      在线人数 : 429
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜寻范围 查询小技巧:
  • 您可在西文检索词汇前后加上"双引号",以获取较精准的检索结果
  • 若欲以作者姓名搜寻,建议至进阶搜寻限定作者字段,可获得较完整数据
  • 进阶搜寻


    jsp.display-item.identifier=請使用永久網址來引用或連結此文件: http://asiair.asia.edu.tw/ir/handle/310904400/2482


    题名: Characterization of β-lactamase (L2) gene in Stenotrophomonas maltophilia
    作者: Cheng shan en
    贡献者: Department of Biotechnology
    关键词: Stenotrophomonas maltophilia;β-lactamase
    日期: 2006
    上传时间: 2009-11-06 06:10:18 (UTC+0)
    出版者: Asia University
    摘要: Stenotrophomonas maltophilia, an aerobic, gram-negative bacillus, displays multiple resistances to common antibiotics. Two indigenous -lactamases encoded by chromosomal genes, L1 and L2, protect S. maltophilia from attack by -lactam antibiotics. Heterogeneity of L2 gene is known to be highly prominent in S. maltophilia. In this study, the L2 sequences is obtained from PCR and further sequenced from the 22 clinical isolates. A series of bioinformatics analysis about L2 is performed, including multiple alignment, allelic variation analysis, phylogenetic analysis, and characteristics prediction. A phylogenetic tree is derived based on the DNA sequences of L2 genes from the 22 clinical isolated and seven L2 genes in the GenBank databases. Nine phylogenetic groups are identified and four L2 phylogenetic groups are reported for the first time. To understand the relationship between genotype and phenotype of L2, the L2 gene is cloned into vector and the resultant recombinant plasmid is transformed into E. coli cell. The expressed L2 activity of recombinant E. coli cell is detected by susceptibility test. No detectable -lactamase activity is expressed in all test strains. AmpR gene, located in the upstream of L2 gene is reported as a transcriptional regulator, affecting the expression of L2 gene. The DNA fragments containing ampR and L2 are got by PCR from four clinical isolates. Similar bioinformatics analysis is carried on. To further investigate the effect of AmpR on the -lactamase activity expression of L2, the -lactamase activity of recombinant E. coli cell containing the constructed ampR-L2-plasmid is evaluated. The -lactamase activities of strains E. coli DH5(pOKM2AmpR-L2) and E. coli DH5(pOKATCC13637AmpR-L2) are higher than that of E. coli DH5(pOK12).
    显示于类别:[生物科技學系] 博碩士論文

    文件中的档案:

    档案 大小格式浏览次数
    0KbUnknown545检视/开启


    在ASIAIR中所有的数据项都受到原著作权保护.


    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 回馈