fluoroorotic acid
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2016 ◽  
Vol 120 (9) ◽  
pp. 1146-1155 ◽  
Author(s):  
Takehito Nakazawa ◽  
Masami Tsuzuki ◽  
Toshikazu Irie ◽  
Masahiro Sakamoto ◽  
Yoichi Honda

Author(s):  
A. Cuellar ◽  
M. Alcolea Palafox ◽  
V.K. Rastogi ◽  
W. Kiefer ◽  
S. Schlücker ◽  
...  

2014 ◽  
Vol 458 (2) ◽  
pp. 343-353 ◽  
Author(s):  
Alyce Merry ◽  
Mengmeng Qiao ◽  
Martin Hasler ◽  
Patricia E. Kuwabara

We show that a mutation in UMP synthase is responsible for the radiation sensitivity of Caenorhabditis elegans rad-6 mutants, and confers resistance to 5-fluoroorotic acid anti-metabolites. We find that disruption of de novo pyrimidine synthesis impairs metabolism and shortens lifespan.


2013 ◽  
Vol 79 (23) ◽  
pp. 7334-7342 ◽  
Author(s):  
Naoki Akasaka ◽  
Hisao Sakoda ◽  
Ryota Hidese ◽  
Yuri Ishii ◽  
Shinsuke Fujiwara

ABSTRACTGluconacetobacter europaeus, one of the microorganisms most commonly used for vinegar production, produces the unfavorable flavor compound acetoin. Since acetoin reduction is important for rice vinegar production, a genetic approach was attempted to reduce acetoin produced byG. europaeusKGMA0119 using specific gene knockout without introducing exogenous antibiotic resistance genes. A uracil-auxotrophic mutant with deletion of the orotate phosphoribosyltransferase gene (pyrE) was first isolated by positive selection using 5-fluoroorotic acid. ThepyrEdisruptant designated KGMA0704 (ΔpyrE) showed 5-fluoroorotic acid resistance. KGMA0704 and thepyrEgene were used for further gene disruption experiments as a host cell and a selectable marker, respectively. Targeted disruption ofaldCorals, which encodes α-acetolactate decarboxylase or α-acetolactate synthase, was attempted in KGMA0704. The disruption of these genes was expected to result in a decrease in acetoin levels. A disruption vector harboring thepyrEmarker within the targeted gene was constructed for double-crossover recombination. The cells of KGMA0704 were transformed with the exogenous DNA using electroporation, and genotypic analyses of the transformants revealed the unique occurrence of targetedaldCoralsgene disruption. ThealdCdisruptant KGMA4004 and thealsdisruptant KGMA5315 were cultivated, and the amount of acetoin was monitored. The acetoin level in KGMA4004 culture was significantly reduced to 0.009% (wt/vol) compared with KGMA0119 (0.042% [wt/vol]), whereas that of KGMA5315 was not affected (0.037% [wt/vol]). This indicates thataldCdisruption is critical for acetoin reduction.G. europaeusKGMA4004 has clear application potential in the production of rice vinegar with less unfavorable flavor.


2012 ◽  
Vol 78 (11) ◽  
pp. 3846-3854 ◽  
Author(s):  
Peter Redder ◽  
Patrick Linder

ABSTRACTWe have developed a range of vectors for allelic replacements inStaphylococcus aureusto facilitate genetic work in this opportunistic pathogen. The central feature of the vector range is a selection/counterselection system that takes advantage of the 5-fluoroorotic acid (FOA) resistance and pyrimidine prototrophy caused by the loss and gain, respectively, of thepyrFandpyrEgenes. This system allows for stringent counterselection of the vectors during the second homologous recombination of a classic allelic replacement. The basic vector pRLY2, which contains thepyrFEgenes fromBacillus subtilis, was combined with chloramphenicol, erythromycin, and tetracycline resistance genes and four different versions of nonreplicative or conditionally replicative origins of replication. The choice between these 12 different pRLY vectors allows for high versatility and ensures that the vectors can be used in virtually any genetic background. Finally, as proof of concept, we present six deletions or modifications of components in theS. aureusdegradosome as well as the operon containing thecshBDEAD box helicase.


2011 ◽  
Vol 153 (3) ◽  
pp. 288-296 ◽  
Author(s):  
Kareen Riviere ◽  
Heidi M. Kieler-Ferguson ◽  
Katherine Jerger ◽  
Francis C. Szoka

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