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. 2003 Jan;185(1):359–370. doi: 10.1128/JB.185.1.359-370.2003

TABLE 3.

Genes with altered transcript amounts in a ΔpurR::aad9 mutant compared to its isogenic purR+ parent

Functional group and R6 genome entry no. Gene Avg fold change in ΔpurR mutanta Protein
Purine gene cluster
    spr0045 purC 13.5 Phosphoribosylaminoimidazole-succinocarboxamide synthetase
    spr0046 purL 26.2 Phosphoribosylformylglycinamide synthetase
    spr0047 purF 12.5 Amidophosphoribosyl transferase
    spr0048 purM 10.6 Phosphoribosylaminoimidazole synthetase
    spr0049 purN 14.6 5′-Phosphoribosylglycinamide transformylase 1
    spr0050 vanZ 18.6 Teicoplanin resistance protein
    spr0051 purH 23.4 Phosphoribosylaminoimidazolecarboxamide formyltransferase
    spr0052 purD 8.7 Phosphoribosylglycinamide synthetase
    spr0053 purE 5.0 Phosphoribosylaminoimidazole carboxylase, catalytic subunit
    spr0054 purK 12.4 Phosphoribosyl glucinamide formyltransferase
    spr0055 spr0055 4.7 Hypothetical protein
    spr0056 purB 3.9 Adenylosuccinate lyase
Purine transport and salvage
    spr0264 spr0264 6.5 Guanine/hypoxanthine transporter?
    spr1128 guaC 5.5 GMP reductase
    spr1662 xpt 3.0 Xanthine phosphoribosyltransferase
    spr1663 pbuX 3.2 Nucleobase:cation symporter for xanthine
Folate metabolism
    spr0266 sulA 2.5 Dihydropteroate synthase
    spr0267 sulB 2.6 Dihydrofolate synthetase
    spr0268 sulC 2.5 GTP cyclohydrolase
    spr0269 sulD 2.1 Aldolase-pyrophosphokinase
    spr1109 fhs 2.2 Formate-tetrahydrofolate ligase
Hypothetical and other
    spr0105 spr0105 2.6 Hypothetical transporter-truncation
    spr0265 spr0265 6.5 Conserved hypothetical protein
    spr0639 copY 2.7 COPAB ATPases metal-fist-type repressor
    spr0641 ctpA 2.2 P-type ATPase, probable copper transporter
    spr1440 spr1440 2.5 Conserved hypothetical protein
    spr1441 oxlT 3.6 Major facilitator:oxalate:formate antiporter
    spr1792 lysA −3.9 Diaminopimelate decarboxylase
    spr1793 purR −27.2 Repressor of purine biosynthetic genes
a

Microarray analyses were performed as described in Materials and Methods on bacteria grown in CDM to mid-exponential phase. Only genes whose transcript amounts showed a relative change of ≥2-fold in three independent experiments are listed. A negative value indicates a decrease in average relative transcript amount.

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