TABLE 2.
Summary of names, substrates and functions of all enzymes used in this study
Name in this study | ORFa Prior name | Predicted function | Observed function | Substrate | Product |
---|---|---|---|---|---|
Strain 81–176 for 6-deoxy-d-altro-heptose pathway | |||||
DdahA | Cjj1426 | C4, C6 dehydratase | C4, C6 dehydratase | GDP-manno-heptose | GDP-6-deoxy-4-keto-d-lyxo-heptose |
DdahB | Cjj1430 | C3, C5 epimerase/C4 reductase | C3 epimerase | GDP-6-deoxy-4-keto-d-lyxo-heptose | GDP-6-deoxy-4-keto-d-arabino heptose |
DdahC | Cjj1427 | C3, C5 epimerase/C4 reductase | C4 reductase | GDP-6-deoxy-4-keto-d-arabino heptose | GDP-6-deoxy-4-keto-d-altro heptose |
WcaG81176 | Cjj1425 WcaG | C4 reductase | C4 reductase | GDP-6-deoxy-4-keto-d-lyxo-heptose | GDP-6-deoxy-d-manno-heptose |
Strain NCTC 11168 for 6-OMe-l-gluco-heptose pathwayb | |||||
MlghA | X | C4 oxidase | Not identified | GDP-manno-heptose | GDP-4-keto-d-lyxo-heptose |
MlghD | Cj1426 | 6-O Methyl Transferase | Not determined | GDP-4-keto-d-lyxo-heptose | GDP-6-OMe-4-keto-d-lyxo-heptose |
MlghB | Cj1430 | C3, C5 epimerase/C4 reductase | C3, C5 epimerase | GDP-6-OMe-4-keto-d-lyxo-heptose | GDP-6-OMe-4-keto-l-xylo-he ptose |
MlghC | Cj1428 | C3, C5 epimerase/C4 reductase | C4 reductase | GDP-6-OMe-4-keto-l-xylo-heptose | GDP-6-OMe-4-keto-l-gluco-heptose |
WcaGNCTC | Cj1427 | C4 reductase | C4 reductase | GDP-6-OMe-4-keto-d-lyxo-heptose | GDP-6-OMe-d-manno-heptose |
a The ORFs and names were as indicated in the genome databases (see Ref. 26) for strain NCTC 11168 and www.ncbi.nlm.nih.gov for strain 81-176. Former names were as previously used in Refs. 24 and 25.
b The enzymes are listed in the anticipated order of participation in the pathway. The assignment of the methyltransferase in the early steps of the pathway after the oxidation step is likely but speculative and awaits biochemical confirmation. Based on this assignment, the natural substrates for MlghB, MlghC, and WcaGNCTC are anticipated to be 6-OMe-4-keto derivatives. The 6-deoxy-4-keto derivatives used as substrates in this study are surrogate substrates obtained by the initial activity of DdahA.