Department of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14853, USA.
Annu Rev Biochem. 2010;79:445-70. doi: 10.1146/annurev-biochem-062608-103436.
Nitric oxide synthases (NOSs) are multidomain metalloproteins first identified in mammals as being responsible for the synthesis of the wide-spread signaling and protective agent nitric oxide (NO). Over the past 10 years, prokaryotic proteins that are homologous to animal NOSs have been identified and characterized, both in terms of enzymology and biological function. Despite some interesting differences in cofactor utilization and redox partners, the bacterial enzymes are in many ways similar to their mammalian NOS (mNOS) counterparts and, as such, have provided insight into the structural and catalytic properties of the NOS family. In particular, spectroscopic studies of thermostable bacterial NOSs have revealed key oxyheme intermediates involved in the oxidation of substrate L-arginine (Arg) to product NO. The biological functions of some bacterial NOSs have only more recently come to light. These studies disclose new roles for NO in biology, such as taking part in toxin biosynthesis, protection against oxidative stress, and regulation of recovery from radiation damage.
一氧化氮合酶(NOSs)是最初在哺乳动物中被鉴定出的多结构域金属蛋白,负责合成广泛存在的信号和保护剂一氧化氮(NO)。在过去的 10 年中,已经鉴定和表征了与动物 NOS 同源的原核蛋白,无论是在酶学还是生物学功能方面。尽管在辅助因子利用和氧化还原伴侣方面存在一些有趣的差异,但细菌酶在许多方面与哺乳动物 NOS(mNOS)相似,因此为 NOS 家族的结构和催化特性提供了深入的了解。特别是,对热稳定细菌 NOS 的光谱研究揭示了参与底物 L-精氨酸(Arg)氧化为产物 NO 的关键氧血红素中间体。一些细菌 NOS 的生物学功能直到最近才被揭示。这些研究揭示了 NO 在生物学中的新作用,例如参与毒素生物合成、抵御氧化应激和调节辐射损伤后的恢复。