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. 1999 Oct;181(19):5930–5939. doi: 10.1128/jb.181.19.5930-5939.1999

TABLE 2.

Comparison of enzyme activities of different molybdoenzymes in R. capsulatus moeA mutant strain R507 and the parental strain KS36

Strain Relevant genotype Enzyme activity (U/mg)a
Xanthine dehydrogenaseb
Nitrate reductasec
DMSO reductased
1 μM Mo 1 mM Mo 1 μM Mo 1 mM Mo 1 μM Mo 1 mM Mo
KS36 ΔnifHDK 0.0067 0.0071 0.14 0.14 0.085 0.22
R507 ΔnifHDK moeA  —e 0.0059
a

Enzyme activities were analyzed in crude extracts after photoheterotrophic growth on RCV medium containing 10 mM ammonium (xanthine dehydrogenase), 10 mM ammonium plus 0.1% nitrate (nitrate reductase) or 10 mM ammonium plus 30 mM DMSO (DMSO reductase). Mean values were calculated from at least six independent measurements. 

b

Xanthine dehydrogenase activity is expressed as micromoles of NAD reduced per minute per milligram of protein. 

c

Nitrate reductase activity is expressed as micromoles of nitrate reduced per minute per milligram of protein. Genes for nitrate reductase from R. sphaeroides were introduced into the corresponding R. capsulatus strains on a replicative plasmid (31). 

d

DMSO reductase activity is expressed as micromoles of DMSO reduced per minute per milligram of protein. 

e

—, below the limit of detection.