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. 2008 Apr 3;105(24):8203–8208. doi: 10.1073/pnas.0709461105

Table 1.

Effects of subunit V isozymes and YHb on NO2-dependent NO production in yeast cells

Strain Subunit V isozyme YHb NO production, pmol NO/g wet weight per min* In vivo turnover rate, pmol NO × 10−1/min per pmol aa3
JM43 Va + 78 ± 32 0.07 ± 0.03
JM43ρ0 Va + 00 ± 20 -
DR11 Va 240 ± 60 0.21 ± 0.05
DR10 Va 20 ± 10 -
GD5b Va + 36 ± 32 0.04 ± 0.03
CT4F Vb + 114 ± 32 0.30 ± 0.08
DW29 Va 168 ± 40 0.18 ± 0.04
DW27 Vb 336 ± 32 0.89 ± 0.08

*Cells (160 mg) were suspended in 2 ml of NO assay buffer and prebubbled for 5 min with N2 to create anoxic conditions. After 5 min of prebubbling NaNO2 was added to 1 mM, and NO production was measured with an NO polarographic electrode.

Turnover rate was calculated by normalizing the rate of NO production to the cytochrome aa3 content of each strain, determined as described (31). Intracellular aa3 contents were 5.6 μM aa3/g wet weight for strains JM43 and DR11; 4.6 μM aa3/g wet weight for strains GD5b and DW29, and 1.9 μM aa3/g wet weight for strains CT4F and DW27. Strains JM43 ρ0 and DR10 lack detectable cytochromes aa3.