Differentiated, Promoter-specific Response of [4Fe-4S] NsrR DNA Binding to Reaction with Nitric Oxide

作者：Crack Jason C; Svistunenko Dimitri A; Munnoch John; Thomson Andrew J; Hutchings Matthew I; Le Brun Nick E^*

来源：JOURNAL OF BIOLOGICAL CHEMISTRY, 2016, 291(16): 8663-8672.

DOI：10.1074/jbc.M115.693192

• DNA-protein interaction
• iron
• iron-sulfur protein
• nitric oxide
• spectroscopy
• DNA-binding protein
• regulator

NsrR is an iron-sulfur cluster protein that regulates the nitric oxide (NO) stress response of many bacteria. NsrR from Streptomyces coelicolor regulates its own expression and that of only two other genes, hmpA1 and hmpA2, which encode HmpA enzymes predicted to detoxify NO. NsrR binds promoter DNA with high affinity only when coordinating a [4Fe-4S] cluster. Here we show that reaction of [4Fe-4S] NsrR with NO affects DNA binding differently depending on the gene promoter. Binding to the hmpA2 promoter was abolished at approximate to 2 NO per cluster, although for the hmpA1 and nsrR promoters, approximate to 4 and approximate to 8 NO molecules, respectively, were required to abolish DNA binding. Spectroscopic and kinetic studies of the NO reaction revealed a rapid, multi-phase, non-concerted process involving up to 8-10 NO molecules per cluster, leading to the formation of several iron-nitrosyl species. A distinct intermediate was observed at approximate to 2 NO per cluster, along with two further intermediates at approximate to 4 and approximate to 6 NO. The NsrR nitrosylation reaction was not significantly affected by DNA binding. These results show that NsrR regulates different promoters in response to different concentrations of NO. Spectroscopic evidence indicates that this is achieved by different NO-FeS complexes.

• 出版日期2016-4-15