A fragment (F13) belongs to the upstream sequence of SMc03267 and four genes encoding a buy Dorsomorphin putative dipeptidase and a putative dipeptide ABC-type transporter. Another fragment (F19) is from SMb20478, part of a gene cluster coding for another dipeptide ABC-transporter. MetN involved in importing methionine also has a fragment of its gene having affinity for ChvI. A fragment found in thiC (F23) and another found in hisB (F1) do not present a directly evident link between the thiamine and

histidine biosynthesis pathways they are respectively involved in but there is an indirect metabolic link that selleck products can be followed in MetaCyc, KEGG and in STRING. ThiC catalyzes the reaction between 5-aminoimidazole ribonucleotide (AIR) and hydroxymethylpyrimidine phosphate (HMP-P) in the thiamine biosynthesis pathway

(Figure 1). AIR is biosynthesized from 5-phosphoribosyl 1-pyrophosphate (PRPP). PRPP is also required for the synthesis of histidine. In STRING this link is made through pur genes, which code for enzymes involved in purine synthesis. Pyrimidine, purine and pyridine nucleotide synthesis pathways are all dependent on the availability of PRPP. Figure 1 5-Phosphoribosyl 1-pyrophosphate (PRPP) metabolic pathway and the potential role of ChvI in regulating downstream biosynthesis pathways. Grey boxes represent genes potentially regulated by ChvI. Uridine-5’-phosphate (UMP), uridine-5’-diphosphate (UDP), uridine-5’-triphosphate (UTP), hydroxymethylpyrimidine phosphate (HMP-P), 4-amino-5-hydroxymethyl-2-methylpyrimidine-pyrophosphate PLX-4720 cell line (HMP-PP), 4-methyl-5-(β-hydroxyethyl)thiazole SPTLC1 phosphate (THZ-P), 5-phospho-β-D-ribosyl-amine (PRA), 5-phospho-ribosyl-glycineamide (GAR), 5’-phosphoribosyl-N-formylglycineamide (FGAR), 5-phosphoribosyl-N-formylglycineamidine (FGAM), 5-aminoimidazole ribonucleotide (AIR), 4-carboxyaminoimidazole ribonucleotide (CAIR), 5’-phosphoribosyl-4-(N-succinocarboxamide)-5-aminoimidazole (SAICAR),

aminoimidazole carboxamide ribonucleotide (AICAR), phosphoribosyl-formamido-carboxamide (FAICAR), inosine-5’-phosphate (IMP), phosphoribosyl-ATP (PR-ATP), phosphoribosyl-AMP (PR-AMP), phosphoribosylformiminoAICAR-P (PRoFAR), phosphoribulosylformimino-AICAR-P (PRFAR), D-erythro-imidazole-glycerol-phosphate (IGP). Following these analyses, we could not find a direct link between these potentially ChvI-regulated genes and the exopolysaccharide biosynthesis pathways, central to one of the most important phenotypes of the chvI mutant strain [10]. This is absolutely consistent with other experimental work that has failed to find direct binding of ChvI to exopolysaccharide synthesis gene upstream regions [17]. However, an indirect link is suggested from the regulation of thiamine and histidine biosynthesis (Figure 1). These pathways are inter-related with the synthesis of pyrimidine and consequently the availability of UTP required for the synthesis of UDP-glucose.