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. 2002 Aug;184(16):4555–4572. doi: 10.1128/JB.184.16.4555-4572.2002

TABLE 1.

Genetic footprinting of E. coli genes related to metabolism of adenylate cofactors NAD(P), CoA, and FAD

Biosynthetic subsystem Gene ORF size (bp) No. of inserts in ORF in strain:
Conclusionb
MG1655 DH10B
NAD nadB 1,620 9 ND N
nadA 1,041 12 ND N
nadC 891 1 4 N
ushA 1,650 6 ND N
pnuC 717 4 ND N
nadR 1,251 6 4 N
pncA 657 2 ND N
pncB 1,200 8 ND N
nadD (ybeN) 639 1 4 Ec
nadE 825 0 1 E
nadF (yfiB) 876 0 0 E
CoA panD 378 2 0 N
panB 792 1 3 N
panE 909 5 2 N
panC 849 1 5 N
coaA 948 0 0 E
coaBC (dfp) 1,290 0 0 E
coaD (kdtB) 477 0 0 E
coaE (yacE) 618 0 0 E
acpS 378 0 0 E
FMN/FAD ribA 588 0 0 E
ribD 1,101 0 0 E
ribB 651 0 0 E
ribH 468 0 0 E
ribE 639 0 0 E
ribF (yaaC) 939 0 0 E
a

The number of transposon insertions per gene in strains MG1655 and DH10B detected after logarithmic aerobic outgrowth for 23 population doublings in rich medium is shown.

b

Assessments of gene essentiality, based on results of genetic footprinting in strains MG1655 and DH10B. E, essential; N, nonessential; ND, not determined.

c

nadD appeared to be nonessential in the two genetic footprinting experiments but was then shown to be essential by a directed-knockout technique.