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1 ase), or by Escherichia coli cysJI (encoding sulfite reductase).
2 e and of dsrC, associated with dissimilatory sulfite reductase).
3 cation is unique and independent of CysI and sulfite reductase.
4 Loss of either protein resulted in decreased sulfite reductase.
5  first report of a coenzyme F(420)-dependent sulfite reductase.
6 sulfite is reduced to H(2)S by dissimilatory sulfite reductase.
7  dehydrogenase, a methanogenesis enzyme, and sulfite reductase, a detoxification enzyme.
8 n suggest that DCP68 is the siroheme protein sulfite reductase, a ferredoxin-dependent enzyme that pa
9                  The consequences of reduced sulfite reductase activity in particular are exacerbated
10 s to grow slowly on metabolites that require sulfite reductase activity.
11 ductase), as well as cytosolic Fe-S enzymes (sulfite reductase and isopropylmalate isomerase).
12 s type of metabolism are DsrAB dissimilatory sulfite reductase and its co-substrate DsrC.
13 -terminal half a dissimilatory-type siroheme sulfite reductase, and Fsr catalyzes the corresponding p
14 oad similarity to the hemoprotein subunit of sulfite reductase but has many significant differences i
15   The key enzyme is DsrAB, the dissimilatory sulfite reductase, but a range of other Dsr proteins is
16                                              Sulfite reductase catalyzes the six-electron reduction o
17 flavin oxidoreductase component of the CysJI sulfite reductase complex (CysJ(8)I(4)), we show that th
18  NrfA nitrite reductase (CXXCK) and the SirA sulfite reductase (CX(12)NKGCH).
19 mparative sequence analysis of dissimilatory sulfite reductase (DSR) genes from closely and distantly
20 lic processes, and profiles of dissimilatory sulfite reductase (dsr) transcripts are consistent with
21 t works as co-substrate of the dissimilatory sulfite reductase DsrAB.
22 CR targeting the 16S rRNA, dissimilatory (bi)sulfite reductase (dsrAB), and dissimilatory arsenate re
23 sion with sequence similarity to the nitrite/sulfite reductase family.
24 mmuno-colocalization with antibodies against sulfite reductase from Arabidopsis thaliana.
25 The initial rate parameters for the purified sulfite reductase from M. tuberculosis were determined u
26 el, highly active, coenzyme F(420)-dependent sulfite reductase (Fsr) with a cell extract specific act
27 t may interact with HdrABC and dissimilatory sulfite reductase gamma subunit (DsrC) to perform novel
28 hic patterns of the functional dissimilatory sulfite reductase gene (dsrA) and the 16S rRNA gene in s
29 ologue of the gamma subunit of dissimilatory sulfite reductase, has been determined by NMR spectrosco
30 he first system was the reduction of E. coli sulfite reductase hemoprotein (SiR-HP).
31    The active center of the Escherichia coli sulfite reductase hemoprotein (SiRHP) is exquisitely des
32 nd nitrite catalyzed by the Escherichia coli sulfite reductase hemoprotein (SiRHP), we have determine
33 s coding for DsrAB, the enzyme dissimilatory sulfite reductase, inevitably also contain the gene codi
34                                              Sulfite reductase is a second autoxidizable electron tra
35 e, the prosthetic group for both nitrite and sulfite reductases, is a methylated, iron-containing mod
36                     Thus the autoxidation of sulfite reductase, like that of the respiratory chain, o
37 ce a sulfate transporter mutant strain and a sulfite reductase mutant strain are fully virulent.
38 ain late evolving archaea, and dissimilatory sulfite reductases of bacteria and archaea.
39              Methanoperedens" genes encoding sulfite reductases of group III (Dsr-LP).
40  staple and C(3) crop rice, we find that the SULFITE REDUCTASE promoter is sufficient for strong bund
41  and gamma subunits of reverse dissimilatory sulfite reductase (rdsr).
42   Like their nitrite reductase counterparts, sulfite reductases require a siroheme cofactor for catal
43 ing the nitrite reductases and dissimilatory sulfite reductase, respectively.
44 al growth when coexpressed with a P. marinus sulfite reductase, revealing that pssm2-Fd can transfer
45                           Assimilatory NADPH-sulfite reductase (SiR) from Escherichia coli is a struc
46 nucleotide polymorphism (SNP) variant in the sulfite reductase (SiR) gene that was significantly asso
47                                              Sulfite reductase (SiR) is an essential enzyme of the su
48 scherichia coli NADPH-dependent assimilatory sulfite reductase (SiR) reduces sulfite by six electrons
49                                        Plant sulfite reductase (SiR; Enzyme Commission 1.8.7.1) catal
50 es (HCO), nitric oxide reductases (NOR), and sulfite reductases (SiR) catalyze the multi-electron and
51                                  Deletion of sulfite reductase (sirA, originally misannotated nirA) r
52 ences or could arise from alterations of the sulfite reductase structure that arise from the isolatio
53 yanobacterial Fds and reactivity with a host sulfite reductase suggest that phage Fds evolved to tran
54 dentification of virus-encoded dissimilatory sulfite reductase suggests SUP05 viruses reprogram their
55 the sulfite scavengers sulfite oxidase (SO), sulfite reductase, UDP-sulfoquinovose synthase, and beta
56                         Previously described sulfite reductases use nicotinamides and cytochromes as
57 uction of sulfite by the DsrAB dissimilatory sulfite reductase, which leads to the production of a Ds