Molecular studies on an ancient gene encoding for carbamoyl-phosphate synthetase

1993 ◽  
Vol 84 (2) ◽  
pp. 119-128 ◽  
Author(s):  
J. P. Schofield

1. Carbamoyl-phosphate synthetase (EC 6.3.5.5.) catalyses the synthesis of carbamoyl phosphate, the immediate precursor of arginine and pyrimidine biosynthesis, and is highly conserved throughout evolution. The large subunit of all carbamoyl-phosphate synthetases sequenced to date comprises two highly homologous halves, the product of a proposed ancestral gene duplication. The sequences of the enzymes of Escherichia coli, Drosophila melanogaster, Saccharomyces cerevisiae, rat and Syrian hamster all have duplications, suggesting that this event occurred in the progenote predating the separation of the major phylae. Until now, only limited data on carbamoyl-phosphate synthetase were available for the primitive eukaryote Dictyostelium discoideum and for the Archaea Methanosarcina barkeri MS. The DNA sequence of the D. discoideum carbamoylphosphate gene and additional sequence for the carbamoyl-phosphate synthetase gene of M. barkeri MS have been determined, and a duplicated structure for both is clearly demonstrated. 2. Genes with ancient duplications provide unique information on their evolution. A study of the intron/exon organization of the rat carbamoylphosphate synthetase I gene and the carbamoylphosphate synthetase hamster II gene in the CAD multi-gene complex shows that at least some of their introns are very old. Evidence is provided that some introns must have been present in the ancestral precursor before its duplication. 3. The human carbamoyl-phosphate synthetase I gene has been isolated and characterized. A human liver cDNA library was constructed and probed for carbamoyl-phosphate synthetase I. A human genomic DNA cosmid library was also probed for the carbamoyl-phosphate synthetase I gene. The cDNA sequence of the human carbamoyl-phosphate synthetase I gene has been determined, and work has been initiated to confirm that at least part of this gene is contained within two cosmids spanning 46 kb. This will enable future studies to be made on mutations in this gene in the rare autosomal recessive deficiency of carbamoyl-phosphate synthetase I.

1995 ◽  
Vol 270 (42) ◽  
pp. 24932-24940 ◽  
Author(s):  
Vincent M. Christoffels ◽  
Maurice J. B. van den Hoff ◽  
Antoon F. M. Moorman ◽  
Wouter H. Lamers

Biochemistry ◽  
1993 ◽  
Vol 32 (1) ◽  
pp. 232-240 ◽  
Author(s):  
Bryant W. Miles ◽  
Shadreck M. Mareya ◽  
Laura E. Post ◽  
David J. Post ◽  
Sun Hee Chang ◽  
...  

2013 ◽  
Vol 59 (6) ◽  
pp. 374-379 ◽  
Author(s):  
Haitian Fang ◽  
Huiyan Liu ◽  
Ning Chen ◽  
Chenglin Zhang ◽  
Xixian Xie ◽  
...  

A major problem when pyrimidine de novo biosynthesis is used for cytidine production is the existence of many negative regulatory factors. Cytidine biosynthesis in Bacillus amyloliquefaciens proceeds via a pathway that is controlled by uridine monophosphate (UMP) through feedback inhibition of carbamoyl phosphate synthetase (CPS), the enzyme that converts CO2, NH3, and glutamine to carbamoyl phosphate. In this study, the gene carB encoding the large subunit of CPS from B. amyloliquefaciens CYT1 was site directed, and the UMP binding sites of feedback inhibition in Bam-CPS are described. The residues Thr-941, Thr-970, and Lys-986 in CPS from B. amyloliquefaciens were subjected to site-directed mutagenesis to alter UMP’s feedback inhibition of CPS. To find feedback-resistant B. amyloliquefaciens, the influence of the T941F, T970A, K986I, T941F/K986I, and T941F/T970A/K986I mutations on CPS enzymatic properties was studied. The recombinant B. amyloliquefaciens with mutated T941F/K986I and T941F/T970A/K986I CPS showed a 3.7- and 5.7-fold increase, respectively, in cytidine production in comparison with the control expressing wild-type CPS, which was more suitable for further application of the cytidine synthesis. To a certain extent, the 5 mutations were found to release the enzyme from UMP inhibition and to improve B. amyloliquefaciens cytidine-producing strains.


2013 ◽  
Vol 80 (1) ◽  
pp. 366-373 ◽  
Author(s):  
Hwa Hui Shin ◽  
Byeong Hee Hwang ◽  
Jeong Hyun Seo ◽  
Hyung Joon Cha

ABSTRACTIt is important to rapidly and selectively detect and analyze pathogenicSalmonella entericasubsp.entericain contaminated food to reduce the morbidity and mortality ofSalmonellainfection and to guarantee food safety. In the present work, we developed an oligonucleotide microarray containing duplicate specific capture probes based on thecarBgene, which encodes the carbamoyl phosphate synthetase large subunit, as a competent biomarker evaluated by genetic analysis to selectively and efficiently detect and discriminate threeS. entericasubsp.entericaserotypes: Choleraesuis, Enteritidis, and Typhimurium. Using the developed microarray system, three serotype targets were successfully analyzed in a range as low as 1.6 to 3.1 nM and were specifically discriminated from each other without nonspecific signals. In addition, the constructed microarray did not have cross-reactivity with other common pathogenic bacteria and even enabled the clear discrimination of the targetSalmonellaserotype from a bacterial mixture. Therefore, these results demonstrated that our novelcarB-based oligonucleotide microarray can be used as an effective and specific detection system forS. entericasubsp.entericaserotypes.


1998 ◽  
Vol 180 (17) ◽  
pp. 4380-4386 ◽  
Author(s):  
Jan Martinussen ◽  
Karin Hammer

ABSTRACT The biosynthesis of carbamoylphosphate is catalyzed by the heterodimeric enzyme carbamoylphosphate synthetase. The genes encoding the two subunits of this enzyme in procaryotes are normally transcribed as an operon, but the gene encoding the large subunit (carB) in Lactococcus lactis is shown to be transcribed as an isolated unit. Carbamoylphosphate is a precursor in the biosynthesis of both pyrimidine nucleotides and arginine. By mutant analysis,L. lactis is shown to possess only onecarB gene; the same gene product is thus required for both biosynthetic pathways. Furthermore, arginine may satisfy the requirement for carbamoylphosphate in pyrimidine biosynthesis through degradation by means of the arginine deiminase pathway. The expression of the carB gene is subject to regulation at the level of transcription by pyrimidines, most probably by an attenuator mechanism. Upstream of the carB gene, an open reading frame showing a high degree of similarity to those of glutathione peroxidases from other organisms was identified.


1999 ◽  
Vol 68 (3) ◽  
pp. 346-356 ◽  
Author(s):  
Dewan Md. Abdullah Abu Musa ◽  
Keiko Kobayashi ◽  
Izumi Yasuda ◽  
Mikio Iijima ◽  
Vincent M. Christoffels ◽  
...  

1996 ◽  
Vol 271 (49) ◽  
pp. 31243-31250 ◽  
Author(s):  
Vincent M. Christoffels ◽  
Maurice J. B. van den Hoff ◽  
Marinus C. Lamers ◽  
Marian A. van Roon ◽  
Piet A. J. de Boer ◽  
...  

2001 ◽  
Vol 52 (2) ◽  
pp. 99-101 ◽  
Author(s):  
Tsutomu Aoshima ◽  
Mitsuharu Kajita ◽  
Yoshitaka Sekido ◽  
Satoshi Kikuchi ◽  
Izumi Yasuda ◽  
...  

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