1.12.1.2 CdSO4 1 mM, complete inhibition 4508 1.12.1.2 CuCl2 0.2 mM, complete inhibition 347 1.12.1.2 cyanide 1 mM, 33% inhibition 118 1.12.1.2 diethyl dicarbonate chemical modification of active site His residues results in reduced enzymatic hydrogenase and diaphorase activities, pH-dependence and kinetics of modifications/inactivation 463 1.12.1.2 DTNB modification of thiol groups of activated enzyme results in rapid inactivation of both activities, modification of the residues of nonactivated enzyme has small effects on the enzyme activities, pH-dependence and kinetics of modifications/inactivation 554 1.12.1.2 glutathione above 0.1 mM: inactivation, up to 0.1 mM: activation 44 1.12.1.2 HgCl2 0.001 mM, complete inhibition 110 1.12.1.2 high ionic strength 200 mM phosphate buffer, 70% inhibition 3693 1.12.1.2 iodoacetate 100 mM, 36% inhibition 93 1.12.1.2 iodoacetate 1 mM, 10% inhibition 93 1.12.1.2 iodoacetic acid modification of thiol groups of activated enzyme results in rapid inactivation of both activities, modification of the residues of nonactivated enzyme has small effects on the enzyme activities, pH-dependence and kinetics of modifications/inactivation 213 1.12.1.2 mercaptoethanol - 1623 1.12.1.2 additional information not inhibited by O2, CO and chelating agents 2 1.12.1.2 additional information no inhibition by O2 2 1.12.1.2 additional information release of one FMN reduces the NAD+ reduction by 90%, but is reversible by addition of excess FMN, insensitivity towards oxygen, with all 4 CN- groups bound to the enzyme, and towards CO 2 1.12.1.2 additional information when light adapted cells are transferred to darkness the expression of hoxE and hoxF is only slightly affected, while the transcript levels of hoxU, hoxY and hoxH are significantly (3-5fold) decreased. Putative regulators of hox gene expression sll0359 is suppressed in dark to a similar extent as hoxU, hoxY and hoxH. The transcriptional regulator lexA shows the opposite expression pattern than that of the hox genes, since it decreases in the light. When cells in microaerobic conditions are transferred to darkness the transcript levels of hoxU, hoxY, hoxH transcripts slightly decrease 2 1.12.1.2 Na+ - 59 1.12.1.2 NAD+ product inhibition; product inhibition 7 1.12.1.2 NADH product inhibition; product inhibition 8 1.12.1.2 Ni2+ 0.5-1 mM, strong inhibition of artificial electron acceptor reduction 38 1.12.1.2 NO - 277 1.12.1.2 O2 slight inhibition of NAD+ reduction and H2 evolution from NADH 9 1.12.1.2 O2 irreversible enzyme inhibition by oxygen occurs if the CN- bound to Ni2+ is irreversibly removed or if the enzyme is reduced by NADH 9 1.12.1.2 O2 incubation of subunits HoxHY with O2 at high potentials causes slow inactivation, but activity is recovered within seconds at potentials below -170 mV at 30°C, even in the presence of 2% O2; incubation of subunits HoxHY with O2 at high potentials causes slow inactivation, but activity is recovered within seconds at potentials below -170 mV at 30°C, even in the presence of 2% O2 9 1.12.1.2 p-chloromercuribenzoate 0.02 mM, complete inhibition, reversed by addition of glutathione 43 1.12.1.2 p-chloromercuribenzoate 0.15 mM, complete inhibition 43 1.12.1.2 Sulfide - 318 1.12.1.2 Sulfide 0.1 mM, 10% inhibition 318 1.12.1.2 Triethanolamine buffer at high concentration 98582 1.12.1.2 Tris-buffer at high concentration 95258