語系:
繁體中文
English
說明(常見問題)
回圖書館首頁
手機版館藏查詢
登入
回首頁
切換:
標籤
|
MARC模式
|
ISBD
Regulation, Function and Potential A...
~
Lu, Shao Yeh.
FindBook
Google Book
Amazon
博客來
Regulation, Function and Potential Applications of Microcin PDI for Medicine and Food Safety.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Regulation, Function and Potential Applications of Microcin PDI for Medicine and Food Safety./
作者:
Lu, Shao Yeh.
出版者:
Ann Arbor : ProQuest Dissertations & Theses, : 2018,
面頁冊數:
113 p.
附註:
Source: Dissertation Abstracts International, Volume: 79-11(E), Section: B.
Contained By:
Dissertation Abstracts International79-11B(E).
標題:
Veterinary science. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10785370
ISBN:
9780438104303
Regulation, Function and Potential Applications of Microcin PDI for Medicine and Food Safety.
Lu, Shao Yeh.
Regulation, Function and Potential Applications of Microcin PDI for Medicine and Food Safety.
- Ann Arbor : ProQuest Dissertations & Theses, 2018 - 113 p.
Source: Dissertation Abstracts International, Volume: 79-11(E), Section: B.
Thesis (Ph.D.)--Washington State University, 2018.
Microcin PDI (mccPDI) is a class IIa microcin that is encoded as a five-locus genetic unit that is borne by a conjugative plasmid. The microcin was first discovered in Escherichia coli strains 25 and 264 (cattle origin) and likely has a significant impact on the microbial composition of E. coli communities in livestock, even contributing to the persistence of antibiotic-resistant strains. This dissertation concerns the mechanism by which the mccPDI phenotype is regulated in the wild-type strains (Chapters 2), how the key effector protein (McpM) kills susceptible bacteria, and how the immunity protein (McpI) protects the mccPDI-producing bacteria (Chapter 3). Up-regulation of mccPDI is controlled by a two-component regulatory system (EnvZ/OmpR) that functions as an on/off switch. Low-salt conditions lead to upregulation of OmpR, which is a transcriptional regulator for both McpM and the cognate ligand on the susceptible cells, OmpF. Deletion of OmpR completely eliminates the mccPDI phenotype (Chapter 1). This on/off osmotic-sensing system is attenuated by the concentration of quorum sensing autoinducer-2 (AI-2) molecules in the culture media. Upregulation of mccPDI corresponds to increasing concentration of AI-2, while down regulation of the system corresponds to the decay of AI-2 as the bacterial population shifts from log-growth into stationary-growth phase. The kinetics of AI-2 expression correspond to the transcriptional pattern of mcpM, and deletion of the quorum sensing system eliminates upregulation of mcpM. It is very likely that sRNAs micC and micF also contribute to the mccPDI regulatory system (Chapter 2). A series of assays demonstrated that mccPDI inhibits the growth of susceptible bacteria when McpM permeabilizes the outer membrane, resulting in cell death. This phenotype can be blocked with the addition of low-molecular mass (200 -- 600 Da) osmoprotectant to the culture media. The mechanism by which McpI protects mccPDI-producing cells is unknown, but experiments described in Chapter 3 show that McpI likely forms asymmetrical trimer structures that may serve to block pores that are formed by McpM.
ISBN: 9780438104303Subjects--Topical Terms:
3172798
Veterinary science.
Regulation, Function and Potential Applications of Microcin PDI for Medicine and Food Safety.
LDR
:03094nmm a2200289 4500
001
2200211
005
20181214130635.5
008
201008s2018 ||||||||||||||||| ||eng d
020
$a
9780438104303
035
$a
(MiAaPQ)AAI10785370
035
$a
(MiAaPQ)wsu:12342
035
$a
AAI10785370
040
$a
MiAaPQ
$c
MiAaPQ
100
1
$a
Lu, Shao Yeh.
$0
(orcid)0000-0003-0504-4232
$3
3426958
245
1 0
$a
Regulation, Function and Potential Applications of Microcin PDI for Medicine and Food Safety.
260
1
$a
Ann Arbor :
$b
ProQuest Dissertations & Theses,
$c
2018
300
$a
113 p.
500
$a
Source: Dissertation Abstracts International, Volume: 79-11(E), Section: B.
500
$a
Adviser: Douglas R. Call.
502
$a
Thesis (Ph.D.)--Washington State University, 2018.
520
$a
Microcin PDI (mccPDI) is a class IIa microcin that is encoded as a five-locus genetic unit that is borne by a conjugative plasmid. The microcin was first discovered in Escherichia coli strains 25 and 264 (cattle origin) and likely has a significant impact on the microbial composition of E. coli communities in livestock, even contributing to the persistence of antibiotic-resistant strains. This dissertation concerns the mechanism by which the mccPDI phenotype is regulated in the wild-type strains (Chapters 2), how the key effector protein (McpM) kills susceptible bacteria, and how the immunity protein (McpI) protects the mccPDI-producing bacteria (Chapter 3). Up-regulation of mccPDI is controlled by a two-component regulatory system (EnvZ/OmpR) that functions as an on/off switch. Low-salt conditions lead to upregulation of OmpR, which is a transcriptional regulator for both McpM and the cognate ligand on the susceptible cells, OmpF. Deletion of OmpR completely eliminates the mccPDI phenotype (Chapter 1). This on/off osmotic-sensing system is attenuated by the concentration of quorum sensing autoinducer-2 (AI-2) molecules in the culture media. Upregulation of mccPDI corresponds to increasing concentration of AI-2, while down regulation of the system corresponds to the decay of AI-2 as the bacterial population shifts from log-growth into stationary-growth phase. The kinetics of AI-2 expression correspond to the transcriptional pattern of mcpM, and deletion of the quorum sensing system eliminates upregulation of mcpM. It is very likely that sRNAs micC and micF also contribute to the mccPDI regulatory system (Chapter 2). A series of assays demonstrated that mccPDI inhibits the growth of susceptible bacteria when McpM permeabilizes the outer membrane, resulting in cell death. This phenotype can be blocked with the addition of low-molecular mass (200 -- 600 Da) osmoprotectant to the culture media. The mechanism by which McpI protects mccPDI-producing cells is unknown, but experiments described in Chapter 3 show that McpI likely forms asymmetrical trimer structures that may serve to block pores that are formed by McpM.
590
$a
School code: 0251.
650
4
$a
Veterinary science.
$3
3172798
690
$a
0778
710
2
$a
Washington State University.
$b
Immunology and Infectious Diseases.
$3
3282952
773
0
$t
Dissertation Abstracts International
$g
79-11B(E).
790
$a
0251
791
$a
Ph.D.
792
$a
2018
793
$a
English
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10785370
筆 0 讀者評論
館藏地:
全部
電子資源
出版年:
卷號:
館藏
1 筆 • 頁數 1 •
1
條碼號
典藏地名稱
館藏流通類別
資料類型
索書號
使用類型
借閱狀態
預約狀態
備註欄
附件
W9376760
電子資源
11.線上閱覽_V
電子書
EB
一般使用(Normal)
在架
0
1 筆 • 頁數 1 •
1
多媒體
評論
新增評論
分享你的心得
Export
取書館
處理中
...
變更密碼
登入