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. 2000 Sep;182(17):4704–4710. doi: 10.1128/jb.182.17.4704-4710.2000

TABLE 3.

Metabolic enzymes involved in glutamylglutamate degradation by P. gingivalis ATCC 33277

Enzyme Substrate Electron carrier Sp act (U/g of protein)a
Glutamylglutamate dipeptidase Glutamylglutamate 21.4 ± 5.30
Glutamate dehydrogenase Glutamate NAD 1,130 ± 128
NADP or MVoxb ND
2-Oxoglutarate oxidoreductase 2-Oxoglutarate and CoA NAD or NADP ND
MVox 11.6 ± 2.96
Succinate-semialdehyde dehydrogenase Succinyl-CoA NADH 788 ± 64.3
NADPH or MVredc ND
Succinate-semialdehyde NAD 1,280 ± 130
NADP or MVox ND
4-Hydroxybutyrate dehydrogenase Succinate-semialdehyde NADH 2,160 ± 226
NADPH 330 ± 140
MVred ND
4-Hydroxybutyrate NAD 325 ± 175
NADP 12.3 ± 2.90
MVox ND
4-Hydroxybutyrate to crotonoyl-CoA 4-Hydroxybutyrate and acetyl-CoA MVred 148 ± 24.5
 −Acetyl-CoA MVred 11.7 ± 2.09
 −Acetyl-CoA + ATP + CoA MVred 10.8 ± 1.06
Butyryl-CoA oxidoreductase Crotonoyl-CoA NADH 1.64 ± 0.74
NADPH ND
MVred 2,150 ± 132
Butyryl-CoA NAD, NADP, or MVox ND
a

Mean ± standard deviation obtained from three independent experiments. ND, not detected. 

b

MVox, oxidized methylviologen. 

c

MVred, reduced methylviologen.