TABLE 2.
Spot no. | Peptide sequence | Identification |
---|---|---|
15 | AIGLVIPELNGK | Glyceraldehyde-3-phosphate dehydrogenase |
IQNVEGVEVTR | ||
16 | AIGLVIPELNGK | Glyceraldehyde-3-phosphate dehydrogenase |
IQNVEGVEVTR | ||
17 | IQNVEGVEVTR | Glyceraldehyde-3-phosphate dehydrogenase |
18 | PAFHD | Ornithine carbamoyltransferase |
HFQDA | ||
19 | FPAEE(I/L)VK | Ornithine carbamoyltransferase |
EVTD | ||
20 | YNQ(I/L)(I/L)R | Enolase |
FEGTEDRE | ||
ETAVG | ||
21 | VVEEVADE(L/I)AEK | Nonphosphorylating glyceraldehyde-3-phosphate dehydrogenase |
GPDNFPF(L/I)G(L/I)K | ||
22 | (L/I)GQDVVF | Phosphoglycerate kinase |
(L/I)GGGDSAAA | Phosphoglycerate kinase | |
23 | (I/L)A(I/L)AM(I/L)ED | Purine nucleoside phosphatase |
DAF(I/L)AGVGT | Purine nucleoside phosphatase |
Assignation of proteins was possible only after reverse genetic analysis. The peptide sequences shown were used to synthesize oligonucleotides, which were in turn used for PCR amplification of the gene from S. agalactiae genomic DNA. The DNA sequence was used to search the database and assign the protein identification.