1995
DOI: 10.1128/jb.177.1.66-74.1995
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A cluster of four genes encoding enzymes for five steps in the folate biosynthetic pathway of Streptococcus pneumoniae

Abstract: Two genes, sulB and sulC, in a folate biosynthetic gene cluster of Streptococcus pneumoniae were identified after determination of the DNA sequence between two previously reported genes, sulA and sulD, in a cloned segment of chromosomal DNA containing a mutation to sulfonamide resistance. The gene products, SulB and SulC, correspond to polypeptides of 49 and 21 kDa, respectively. SulC has GTP cyclohydrolase activity and catalyzes the first step in the folate biosynthetic pathway. SulB apparently has dihydrofol… Show more

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Cited by 40 publications
(27 citation statements)
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“…Although its counterpart in C. elegans appears to be a domain in a much larger protein, this may be an anomaly of that invertebrate species. A similar case was observed in the folate biosynthetic system, present in Pneumocystis carinii, where four domains present as single proteins in other species (21) are joined together to make a single polyprotein (42). Accordingly, the polypeptide components of RNase HII in human cells may be similar in size to that in S. pneumoniae.…”
Section: Discussionmentioning
confidence: 67%
“…Although its counterpart in C. elegans appears to be a domain in a much larger protein, this may be an anomaly of that invertebrate species. A similar case was observed in the folate biosynthetic system, present in Pneumocystis carinii, where four domains present as single proteins in other species (21) are joined together to make a single polyprotein (42). Accordingly, the polypeptide components of RNase HII in human cells may be similar in size to that in S. pneumoniae.…”
Section: Discussionmentioning
confidence: 67%
“…Single nucleotide mutations were found in the expressed coding region of the FPGS gene for cDNA from each mutant cell line (Table III). 50 …”
Section: Levels Of the Target Enzyme For Ddathf And Of The Enzymes Inmentioning
confidence: 99%
“…To investigate whether Mga Spn influenced the activity of a particular promoter in vivo, we constructed a pneumococcal strain designed to overproduce Mga Spn . First, we constructed the PsulA::mga fusion gene, in which the Pmga promoter of the mga Spn gene was replaced with the promoter of the pneumococcal sulA gene (PsulA) (18,32). The fusion gene was then inserted into pDL287 (21), generating the pDLPsulA::mga recombinant.…”
Section: Figmentioning
confidence: 99%