Language:
English
繁體中文
Help
回圖書館首頁
手機版館藏查詢
Login
Back
Switch To:
Labeled
|
MARC Mode
|
ISBD
Molecular basis for uranium toxicity.
~
Burbank, Katherine Ann.
Linked to FindBook
Google Book
Amazon
博客來
Molecular basis for uranium toxicity.
Record Type:
Electronic resources : Monograph/item
Title/Author:
Molecular basis for uranium toxicity./
Author:
Burbank, Katherine Ann.
Description:
254 p.
Notes:
Source: Dissertation Abstracts International, Volume: 75-11(E), Section: B.
Contained By:
Dissertation Abstracts International75-11B(E).
Subject:
Biochemistry. -
Online resource:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3630532
ISBN:
9781321085167
Molecular basis for uranium toxicity.
Burbank, Katherine Ann.
Molecular basis for uranium toxicity.
- 254 p.
Source: Dissertation Abstracts International, Volume: 75-11(E), Section: B.
Thesis (Ph.D.)--Montana State University, 2014.
This item must not be sold to any third party vendors.
Environmental and health problems associated with uranium extend well beyond its radioactive properties. Hexavelent uranium is a common environmental contaminant that reacts with water to form the dioxo-uranium cation, UO22+. Environmental uranium contamination is the result of a number of activities including uranium mining, production and use of depleted uranium for military purposes, storage and disposal of nuclear weaponry, and fuel for nuclear power plants. Despite the potential importance of the interaction of UO22+ with biologically relevant molecules, only limited molecular insight is available. In a recent publication, the presence of UO22+ in submicromolar concentrations was shown to affect ethanol metabolism in Pseudomonas spp. by displacing the Ca2+ of the pyrroloquinoline quinone (PQQ) cofactor. Accordingly, the interaction of UO2 2+ with PQQ is used here as a starting point to carry out both an in vitro and in silico analysis of UO2 2+ and its interactions with biologically relevant cofactors and metabolites. This work represents a proposed molecular mechanism of uranium toxicity in bacteria, and has relevance for uranium toxicity in many living systems. The structural insights from modeling allow us to expand the scope of potential uranium toxicity to other systems by considering the favorable coordination mode to pyridine nitrogen adjacent to carboxylic and/or carbonyl groups. Consequently, the recent discovery of uranium toxicity at submicromolar levels in bacteria provides relevance to serious environmental and public health issues in the light of current EPA regulation of 0.13 muM uranium limit in drinking water.
ISBN: 9781321085167Subjects--Topical Terms:
518028
Biochemistry.
Molecular basis for uranium toxicity.
LDR
:02685nmm a2200313 4500
001
2059479
005
20150805065220.5
008
170521s2014 ||||||||||||||||| ||eng d
020
$a
9781321085167
035
$a
(MiAaPQ)AAI3630532
035
$a
AAI3630532
040
$a
MiAaPQ
$c
MiAaPQ
100
1
$a
Burbank, Katherine Ann.
$3
3173555
245
1 0
$a
Molecular basis for uranium toxicity.
300
$a
254 p.
500
$a
Source: Dissertation Abstracts International, Volume: 75-11(E), Section: B.
500
$a
Advisers: Brent M. Peyton; Robert A. Walker.
502
$a
Thesis (Ph.D.)--Montana State University, 2014.
506
$a
This item must not be sold to any third party vendors.
506
$a
This item must not be added to any third party search indexes.
520
$a
Environmental and health problems associated with uranium extend well beyond its radioactive properties. Hexavelent uranium is a common environmental contaminant that reacts with water to form the dioxo-uranium cation, UO22+. Environmental uranium contamination is the result of a number of activities including uranium mining, production and use of depleted uranium for military purposes, storage and disposal of nuclear weaponry, and fuel for nuclear power plants. Despite the potential importance of the interaction of UO22+ with biologically relevant molecules, only limited molecular insight is available. In a recent publication, the presence of UO22+ in submicromolar concentrations was shown to affect ethanol metabolism in Pseudomonas spp. by displacing the Ca2+ of the pyrroloquinoline quinone (PQQ) cofactor. Accordingly, the interaction of UO2 2+ with PQQ is used here as a starting point to carry out both an in vitro and in silico analysis of UO2 2+ and its interactions with biologically relevant cofactors and metabolites. This work represents a proposed molecular mechanism of uranium toxicity in bacteria, and has relevance for uranium toxicity in many living systems. The structural insights from modeling allow us to expand the scope of potential uranium toxicity to other systems by considering the favorable coordination mode to pyridine nitrogen adjacent to carboxylic and/or carbonyl groups. Consequently, the recent discovery of uranium toxicity at submicromolar levels in bacteria provides relevance to serious environmental and public health issues in the light of current EPA regulation of 0.13 muM uranium limit in drinking water.
590
$a
School code: 0137.
650
4
$a
Biochemistry.
$3
518028
650
4
$a
Inorganic chemistry.
$3
3173556
650
4
$a
Chemistry.
$3
516420
690
$a
0487
690
$a
0488
690
$a
0485
710
2
$a
Montana State University.
$b
Chemistry and Biochemistry.
$3
2100488
773
0
$t
Dissertation Abstracts International
$g
75-11B(E).
790
$a
0137
791
$a
Ph.D.
792
$a
2014
793
$a
English
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3630532
based on 0 review(s)
Location:
ALL
電子資源
Year:
Volume Number:
Items
1 records • Pages 1 •
1
Inventory Number
Location Name
Item Class
Material type
Call number
Usage Class
Loan Status
No. of reservations
Opac note
Attachments
W9292137
電子資源
11.線上閱覽_V
電子書
EB
一般使用(Normal)
On shelf
0
1 records • Pages 1 •
1
Multimedia
Reviews
Add a review
and share your thoughts with other readers
Export
pickup library
Processing
...
Change password
Login