Rigano C, Aliotta G
Biochim Biophys Acta. 1975 Mar 28;384(1):37-45. doi: 10.1016/0005-2744(75)90093-5.
Studies on nitrate reductase (NAD(P)H:nitrate oxidoreductases EC 1.6.6.2) of Cyanidium caldarium revealed that the enzyme is inhibited by excess of electron donor, NADPH, reduced benzylviologen and FMN. Also dithionite, used to reduce benzylviologen and FMN, inactivates nitrate reductase: however, FMN at an optimal concentration and nitrate, added before the dithionite, protect the enzyme against this inactivation. Cyanide, cyanate and carbamyl phosphate inhibit the enzyme competitively with respect to nitrate, and Ki values are reported. Organic mercurials, 0.1 mM, act preferentially on NADPH activity, whereas Ag+ and Hg-2+ at the same concentration inactivate 80--90% of the benzylviologen and FMN activities. ADP is very poor inhibitor. Urea 4 M in 2 h destroys 90% of the NADPH activity and only 30% of the benzylviologen and FMN activities. The apparent Km values for NADPH, benzylviologen, FMN and nitrate have been determined.
对嗜热蓝藻硝酸还原酶(NAD(P)H:硝酸氧化还原酶,EC 1.6.6.2)的研究表明,该酶会受到过量电子供体、NADPH、还原型苄基紫精和FMN的抑制。用于还原苄基紫精和FMN的连二亚硫酸盐也会使硝酸还原酶失活:然而,在连二亚硫酸盐之前添加的最佳浓度的FMN和硝酸盐可保护该酶免受这种失活作用。氰化物、氰酸盐和氨基甲酰磷酸相对于硝酸盐竞争性抑制该酶,并报告了Ki值。0.1 mM的有机汞优先作用于NADPH活性,而相同浓度的Ag+和Hg2+会使80%-90%的苄基紫精和FMN活性失活。ADP是非常弱的抑制剂。4 M尿素在2小时内会破坏90%的NADPH活性,而仅破坏30%的苄基紫精和FMN活性。已测定了NADPH、苄基紫精、FMN和硝酸盐的表观Km值。