ライフサイエンスコーパス: sulfite

1 t rate by reaction with sulfide but not with sulfite.

2 which is then partitioned to thiosulfate or sulfite.

3 s showed sensitivity and overaccumulation of sulfite.

4 kely metabolite of thiosulfate assimilation, sulfite.

5 reflecting a decrease in the ability to bind sulfite.

6 f ammonium with o-phthaldialdehyde (OPA) and sulfite.

7 ains that function together to reduce APS to sulfite.

8 ur compounds or reduction of organic-sourced sulfite.

9 ancement increased with the concentration of sulfite.

10 mproved by 29 times in the presence of 20 mM sulfite.

11 rapidly oxidised sulfide to thiosulfate and sulfite.

12 ts dibenzothiophene to 2-hydroxybiphenyl and sulfite.

13 ) during the free radical chain oxidation of sulfite.

14 fide and unexpectedly, when it is exposed to sulfite.

15 reacts with OPA and forms in the presence of sulfite a product, which can be detected by spectrophoto

16 Sulfite, a major dithionite oxidation product, lowered k

17 nderstood, particularly for the reduction of sulfite-a key intermediate in the pathway.

18 e reductase was enhanced, leading to further sulfite accumulation in SIR Ri plants.

19 in protecting leaves against the toxicity of sulfite accumulation.

20 ic red wines produced without sulfur dioxide/sulfites addition are comparable to conventional red win

21 ic red wines produced without sulfur dioxide/sulfites addition in comparison to those of eight conven

22 udies (stabilizations of the covalent FAD-N5-sulfite adduct and p-quinonoid form of 8-mercapto-FAD),

23 model wine was present in free and hydrogen sulfite adduct forms and the measured total, free and pe

24 The presence of a prFMN sulfite-adduct in one of the UbiD crystal structures con

25 In flow chamber experiments involving sulfite aerosol and gas-phase glyoxal with only 1 min re

26 nd Mn(II) caused damage to DNA while neither sulfite alone nor metal ions alone did have the same eff

27 lly, the effect of the reducing agent sodium sulfite also was evaluated to characterize the nature of

28 and (v) sequential elimination via a cyclic sulfite and a cyclobutyl triflate.

29 Isethionate is then cleaved to sulfite and acetaldehyde by a previously uncharacterized

30 ted C-S bond cleavage of isethionate to form sulfite and acetaldehyde.

31 the two-electron reduction of APS and forms sulfite and adenosine 5'-monophospahate (AMP).

32 her reactive sulfur species (RSS), including sulfite and bisulfite, as well as sulfane sulfur species

33 vasculature system, where it is reduced into sulfite and finally sulfide within the subcellular organ

34 transfer in the direction of thiosulfate to sulfite and glutathione persulfide; sulfur transfer in t

35 ctivity of human rhodanese to cyanide versus sulfite and might be important in differences in suscept

36 the central cofactor in a conserved class of sulfite and nitrite reductases that catalyze the six-ele

37 Other sulfite compounds, namely sodium sulfite and potassium metabisulfite, also promote the li

38 sulfite-sensitive mutants accumulate applied sulfite and show a decline in glutathione levels.

39 suggests an efficient oxidation pathway via sulfite and sulfate radical anions on droplets possibly

40 oxidize sulfide (H2 S, HS(-) and S(2-) ) to sulfite and thiosulfate via polysulfide.

41 ection for simultaneous analysis of sulfate, sulfite, and chloride in human urine, plasma, and sweat

42 ple thiophilic acceptors, including sulfide, sulfite, and glutathione, to form as products, hydrodisu

43 n and to 2.4 A resolution in the presence of sulfite, and the C185A variant to 2.8 A resolution.

44 gradation rate of MO was greatly enhanced by sulfite, and the enhancement increased with the concentr

45 spontaneously desulfinated to succinate and sulfite; and (iii) whereas succinate enters the central

46 any reactive radical species, we report that sulfite anion radical efficiently substitutes the three

47 icals generated by the reactions of sulfite (sulfite anions or bisulfite anions) with holes or hydrox

48 ts in maintaining sulfite homeostasis, where sulfite appears to act as an orchestrating signal molecu

49 and activity levels are likewise promoted by sulfite application as compared with water injection con

50 Exogenous sulfite application induced up-regulation of the sulfite

51 Resistance to high sulfite application is manifested by fast sulfite disapp

52 -stressed wild-type plants were resistant to sulfite applications, but SO RNA interference plants sho

53 containing compounds, augmented by exogenous sulfite applications, underlines the role of SO and othe

54 Sulfites are food additives found in a large variety of

55 ned in competition kinetic experiments using sulfite as a competitor.

56 r of their ability to induce DNA damage with sulfite as follows: Fe(III) > Co(II) > Cu(II) > Cr(VI) >

57 hat it is essential for growth on sulfate or sulfite as the sole sulfur source and, further, that the

58 Oxidation of H(2)S by SQOR with sulfite as the sulfane sulfur acceptor is rapid and high

59 caftaric acid were found in wines containing sulfites as a preservative.

60 linear in the range 0.032-0.320 mg L(-1) of sulfite (as SO2), with a correlation coefficient of 0.99

61 d in an Escherichia coli strain deficient in sulfite assimilation, pssm2-Fd complemented bacterial gr

62 In addition to the BiOBr/MO system, the sulfite-assisted photocatalysis approach has been succes

63 vities of the cell are incapable of reducing sulfite at a rate sufficient to allow growth.

64 another low pH form, whereas reduction with sulfite at higher pH values gives a mixture of Species 1

65 NA damage induced by radicals generated from sulfite autoxidation using cyclic voltammetry (CV) and e

66 R is consistent with glutathione rather than sulfite being the predominant acceptor at physiologicall

67 An apparent sulfite-binding pocket at the protein-protein interface

68 An amperometric sulfite biosensor was fabricated using SO(X)/Fe(3)O(4)@G

69 ion to form SO(2), which becomes hydrated to sulfite/bisulfite (S(IV)).

70 idation and insight into the impact of these sulfite bound carbonyls on antimicrobial and antioxidant

71 ithout increasing concentrations of free and sulfite-bound acetaldehyde.

72 ration from components of the medium (mainly sulfite) but not from sulfate.

73 iderable photocurrent for photo-oxidation of sulfite, but generated significantly reduced photocurren

74 d many bacteria, this compound is reduced to sulfite by APS reductase (APR); in fungi and some cyanob

75 ate (PAPS), is necessary before reduction to sulfite by PAPS reductase (PAPR).

76 The 1,2-eliminations in cyclic carbonate and sulfite by regioselective abstraction of methine protons

77 ytoplasmic membrane for further oxidation to sulfite by the dissimilatory reductase DsrAB is incomple

78 valent anions such as oxalate, carbonate and sulfite can act as powerful latent electron donors when

79 of this species prepared with (33)S-labeled sulfite clearly show the presence of coordinated sulfate

80 wever, dechlorination of reacted N-CNTs with sulfite completely suppresses N-CNT toxicity.

81 rom dissolution at lower temperatures to TMI-sulfite complex formation at higher temperatures.

82 Other sulfite compounds, namely sodium sulfite and potassium m

83 spot test method) were used to determine the sulfite concentration of 10 different commercially sulfi

84 However, under pathological conditions when sulfite concentrations are high, sulfite could compete w

85 Four samples presented higher phosphate and sulfite concentrations than those permitted by Brazilian

86 "allergic-like" symptoms upon consumption of sulfite containing foods.

87 on, did not correlate with total phenolic or sulfite content.

88 Overall, satisfactory sulfite conversion and hydrogen production efficiencies

89 itions when sulfite concentrations are high, sulfite could compete with sulfide for addition to the a

90 e (SO) is found in animals and plants, while sulfite dehydrogenase (SDH) is found in bacteria.

91 ively charged substitution R55K in bacterial sulfite dehydrogenase (SDH).

92 ana plant sulfite oxidase, and the bacterial sulfite dehydrogenase from Starkeya novella.

93 both metabolisms could facilitate exergonic, sulfite-dependent, anaerobic oxidation of methane to met

94 AB is a protein-based trisulfide, in which a sulfite-derived sulfur is bridging two conserved cystein

95 There are several sulfite detection methods available in the literature th

96 ant SO (PSO) also plays an important role in sulfite detoxification and in addition serves as an inte

97 sulfur dioxide was hydrated and bound as the sulfite dianion in the Zn5 L6 structure.

98 Subsequent in situ oxidation of the sulfite dianion resulted in a sulfate dianion bound with

99 ased sulfate uptake but sulfate reduction to sulfite did not seem to be regulated.

100 Due to the chemical reactivity of sulfite, dilute formaldehyde is used as a reagent to for

101 gh sulfite application is manifested by fast sulfite disappearance and an increase in glutathione lev

102 dium and chemical oxidation to carry out the sulfite electro-oxidation and hydrogen evolution reactio

103 ficient electrochemical flow cell system for sulfite electrolysis and hydrogen production, with poten

104 Herein, the performance and stability during sulfite electrolysis under alkaline conditions are evalu

105 Herein, we have developed a sulfite-enhanced visible-light-driven photodegradation p

106 carbonate (EC), dimethyl carbonate, ethylene sulfite (ES), and their combinations as electrolyte solv

107 ted by sulfide, a precursor to mitochondrial sulfite formation.

108 mes that allow intestinal bacteria to access sulfite from taurine have not yet been identified.

109 sulfur from glutathione persulfide (GSSH) to sulfite generating thiosulfate and from thiosulfate to c

110 tially catalyze sulfur transfer from GSSH to sulfite, generating thiosulfate and glutathione.

111 We demonstrate that, in addition to sulfite, glutathione functions as a persulfide acceptor

112 on being: H2S --> glutathione persulfide --> sulfite --> sulfate, than with a more convoluted route t

113 fate (H(2) S + SO42- S2O32- + H(2) O) and to sulfite (H(2) S + 3 SO42- 4 SO32- + 2H(+) ), are only mo

114 d that besides HMS, its isomer hydroxymethyl sulfite (HMSi), which has not been identified in atmosph

115 er sulfite network components in maintaining sulfite homeostasis, where sulfite appears to act as an

116 ssible to observe and sometimes quantify the sulfite, hydrate, and acetal forms of the carbonyl compo

117 s PRF is poised to metabolize thiosulfate to sulfite in a sulfur assimilation pathway rather than in

118 ate the disadvantageous presence of residual sulfite in crystal sugar.

119 was evaluated with 96.46% recovery of added sulfite in red wine and 1.7% and 3.3% within and between

120 the determination of citrate, phosphate and sulfite in seafood by capillary zone electrophoresis wit

121 action method (HS-SDME) for determination of sulfite in the form of sulfur dioxide was developed.

122 It was found that sulfite in the presence of Co(II), Cu(II), Cr(VI), Fe(II

123 aqueous phase reactions of benzoic acid with sulfite in the presence of Fe(3+) under various conditio

124 oxidation of alkanesulfonate to aldehyde and sulfite in the presence of O2 and FMNH2.

125 in the overall reaction process whereby the sulfite, in the presence of transition metals, may cause

126 imum concentration of a transition metal for sulfite induced DNA damage revealed that electrochemical

127 is also formed when sulfide is added to the sulfite-induced CT intermediate, representing a new mech

128 SiR transcript and activity within 30 min of sulfite injection into Arabidopsis and tomato leaves.

129 rn about food preservation, the reduction of sulfite input plays a major role in the wine industry.

130 osphate co-factors and converts cysteine and sulfite into cysteic acid and hydrogen sulfide, respecti

131 te oxidation to sulfate and incorporation of sulfite into sulfoquinovosyl diacylglycerols were not su

132 The electrochemical oxidation of sulfite ions offers encouraging advantages for large-sca

133 stance to ectopically applied sulfur dioxide/sulfite is a function of SiR expression levels and that

134 ts for the removal of water pollutants since sulfite is a waste from flue gas desulfurization process

135 In biological systems, the detoxification of sulfite is catalyzed by the sulfite-oxidizing enzymes (S

136 eas succinate enters the central metabolism, sulfite is detoxified by the previously identified putat

137 The higher sulfite is likely the main reason for the initiation of

138 The results suggest that sulfite is rapidly autoxidized in the presence of Co(II)

139 ed to acetyl-CoA by a dehydrogenase, and the sulfite is reduced to H(2)S by dissimilatory sulfite red

140 s a role in the protection of plants against sulfite is supported by the rapid up-regulation of SiR t

141 We propose that sulfite is the physiological acceptor of the sulfane sul

142 1A mutation causing a 5-fold increase in the sulfite K(m) value, perhaps reflecting a decrease in the

143 Biosensor measured sulfite level in red and white wines.

144 conditions, the sulfite network can control sulfite levels in the absence of SO activity.

145 Little is known about the homeostasis of sulfite levels, a cytotoxic by-product of plant sulfur t

146 ls were not sufficient to maintain low basal sulfite levels, resulting in accumulative leaf damage in

147 is necessary to cope with rising endogenous sulfite levels.

148 at it has excellent electrocatalysis towards sulfite, lower detection limit, higher storage stability

149 zed glycyl radical enzyme (GRE), isethionate sulfite-lyase (IslA).

150 Among these, sulfites may induce adverse effects after ingestion.

151 re found for specific Kraft, mechanical, and sulfite mills, suggesting yet unidentified causative age

152 Sulfite molecules lead to desirable morphology and compo

153 However, under nonstressed conditions, the sulfite network can control sulfite levels in the absenc

154 cations, underlines the role of SO and other sulfite network components in maintaining sulfite homeos

155 opersicum) wild-type leaves, while the other sulfite network components were down-regulated.

156 ic pathways, we followed key elements of the sulfite network enzymes that include adenosine-5'-phosph

157 f nitrite, which need not be the case in the sulfite/nitrite reductase family.

158 ell-known stimulatory effect of the oxyanion sulfite on MgATP hydrolysis.

159 Sulfite, on the other hand, has a significantly less neg

160 ependent oxidation of S degrees , sulfide or sulfite or H(2)oxidation.

161 Cyanide, sulfite, or sulfide can act as the sulfane sulfur accept

162 nter of the pathogenic R160Q mutant of human sulfite oxidase (hSO) confirms the presence of three dis

163 dies on the pathogenic R160Q mutant of human sulfite oxidase (HSO) have shown that Mo-heme intramolec

164 hotosystem I, cytochrome c (cyt c) and human sulfite oxidase (hSOX).

165 A sulfite oxidase (SO(X)) (EC 1.8.3.1) purified from Syzyg

166 Sulfite oxidase (SO) catalyzes the physiologically criti

167 Dimethylsulfoxide reductase (DMSOR) and sulfite oxidase (SO) families were the most widespread m

168 Sulfite oxidase (SO) is a vitally important molybdenum e

169 Sulfite oxidase (SO) is found in animals and plants, whi

170 The Mo(V) state of the molybdoenzyme sulfite oxidase (SO) is paramagnetic and can be studied

171 sulfate reductase and the sulfite scavengers sulfite oxidase (SO), sulfite reductase, UDP-sulfoquinov

172 relate to the reduced and oxidized forms of sulfite oxidase (SO).

173 Sulfite oxidase (SUOX) expression and the drug-transport

174 o either the xanthine dehydrogenase (XDH) or sulfite oxidase (SUOX) families, and these have pyranopt

175 persulfide dioxygenase (PDO), rhodanese, and sulfite oxidase and converts H2S to thiosulfate and sulf

176 Saccharomyces cerevisiae lacking sulfite oxidase and deleted of flavohemoglobin showed an

177 The physiological implications of plant sulfite oxidase as a copious generator of superoxide are

178 Isolated sulfite oxidase deficiency (ISOD) causes severe intellec

179 In humans, sulfite oxidase deficiency is an inherited recessive dis

180 for confirmatory testing of cystic fibrosis, sulfite oxidase deficiency, urolithiasis, and other diso

181 affecting the type of reactions catalyzed by sulfite oxidase family enzymes.

182 ent response of the catalytic cycle of human sulfite oxidase immobilized on an electrode.

183 The crystal structure of chicken liver sulfite oxidase indicated that this residue, Cys185 in c

184 te forms of the molybdenum-containing enzyme sulfite oxidase possess a b-type cytochrome prosthetic g

185 Peroxisomal sulfite oxidase transcripts and activity levels are like

186 sulfite oxidase, Arabidopsis thaliana plant sulfite oxidase, and the bacterial sulfite dehydrogenase

187 remarkably similar to that found in chicken sulfite oxidase, Arabidopsis thaliana plant sulfite oxid

188 f this residue in the catalytic mechanism of sulfite oxidase, serine and alanine variants at position

189 subsequent reconstitution of MoCo-free human sulfite oxidase-molybdenum domain yielding a fully activ

190 calculations are extended to oxo transfer by sulfite oxidase.

191 rsulfide dioxygenase (ETHE1), rhodanese, and sulfite oxidase.

192 is remarkably similar to the low-pH form of sulfite oxidase.

193 Sulfite oxidases are metalloenzymes that oxidize sulfite

194 Sulfite oxidases have been wired to electrode surfaces,

195 s the reason for the decrease in activity of sulfite oxidases upon immobilization.

196 In vertebrate sulfite oxidases, the electrons generated at the Mo cent

197 We found that sulfite oxidation mediated by EPO/H(2)O(2) induced the f

198 Increased sulfite oxidation to sulfate and incorporation of sulfit

199 indicate that neither variant is capable of sulfite oxidation.

200 Sulfite oxidizing enzymes (SOEs) are molybdenum cofactor

201 2)O/OH(-) ligand bound to Mo as found in the sulfite oxidizing enzymes of the same family.

202 etoxification of sulfite is catalyzed by the sulfite-oxidizing enzymes (SOEs), which interact with an

203 similar results were observed for samples of sulfite-oxidizing enzymes from other organisms that were

204 All reported sulfite-oxidizing enzymes have a conserved arginine in t

205 sis of the possible mechanistic pathways for sulfite-oxidizing enzymes is presented and related to av

206 The DNA damage induced by sulfite plus Co(II), Cr(VI), and Fe(III) was inhibited b

207 ons were measured by HPLC using a stable OPA/sulfite precolumn derivatization and an electrochemical

208 ed wild-type plants, while expression of the sulfite producer, adenosine-5'-phosphosulfate reductase,

209 subsequent steps by thioredoxin to yield the sulfite product.

210 e concentration of 10 different commercially sulfited products.

211 n rapidly oxidise sulfide to thiosulfate and sulfite, providing the foundation for using heterotrophi

212 Studies using hole scavengers suggest that sulfite radicals generated by the reactions of sulfite (

213 s the presence of coordinated sulfate in the sulfite-reduced low-pH form of the plant enzyme.

214 f infected oat tissue homogenate with sodium sulfite reduces transmission of the purified virus by ap

215 The combination of sulfite reducing Clostridium spp. with SRB may improve g

216 rs for anaerobic respiration in sulfate- and sulfite-reducing bacteria.

217 NrfA nitrite reductase (CXXCK) and the SirA sulfite reductase (CX(12)NKGCH).

218 lic processes, and profiles of dissimilatory sulfite reductase (dsr) transcripts are consistent with

219 CR targeting the 16S rRNA, dissimilatory (bi)sulfite reductase (dsrAB), and dissimilatory arsenate re

220 and gamma subunits of reverse dissimilatory sulfite reductase (rdsr).

221 Assimilatory NADPH-sulfite reductase (SiR) from Escherichia coli is a struc

222 Sulfite reductase (SiR) is an essential enzyme of the su

223 Plant sulfite reductase (SiR; Enzyme Commission 1.8.7.1) catal

224 Deletion of sulfite reductase (sirA, originally misannotated nirA) r

225 The consequences of reduced sulfite reductase activity in particular are exacerbated

226 ductase), as well as cytosolic Fe-S enzymes (sulfite reductase and isopropylmalate isomerase).

227 Sulfite reductase catalyzes the six-electron reduction o

228 flavin oxidoreductase component of the CysJI sulfite reductase complex (CysJ(8)I(4)), we show that th

229 sion with sequence similarity to the nitrite/sulfite reductase family.

230 The initial rate parameters for the purified sulfite reductase from M. tuberculosis were determined u

231 t may interact with HdrABC and dissimilatory sulfite reductase gamma subunit (DsrC) to perform novel

232 hic patterns of the functional dissimilatory sulfite reductase gene (dsrA) and the 16S rRNA gene in s

233 ce a sulfate transporter mutant strain and a sulfite reductase mutant strain are fully virulent.

234 yanobacterial Fds and reactivity with a host sulfite reductase suggest that phage Fds evolved to tran

235 dentification of virus-encoded dissimilatory sulfite reductase suggests SUP05 viruses reprogram their

236 ase), or by Escherichia coli cysJI (encoding sulfite reductase).

237 dehydrogenase, a methanogenesis enzyme, and sulfite reductase, a detoxification enzyme.

238 s coding for DsrAB, the enzyme dissimilatory sulfite reductase, inevitably also contain the gene codi

239 ing the nitrite reductases and dissimilatory sulfite reductase, respectively.

240 al growth when coexpressed with a P. marinus sulfite reductase, revealing that pssm2-Fd can transfer

241 the sulfite scavengers sulfite oxidase (SO), sulfite reductase, UDP-sulfoquinovose synthase, and beta

242 cation is unique and independent of CysI and sulfite reductase.

243 sulfite is reduced to H(2)S by dissimilatory sulfite reductase.

244 Loss of either protein resulted in decreased sulfite reductase.

245 Like their nitrite reductase counterparts, sulfite reductases require a siroheme cofactor for catal

246 anaerobic S(0) reduction, anaerobic sulfate/sulfite reduction and anaerobic respiration of organic s

247 acterial system, we show that the product of sulfite reduction by DsrAB is a protein-based trisulfide

248 C biosynthesis and that pseudomonads utilize sulfite reduction enzymology distinct from that of E. co

249 Sulfite reduction in Mycobacterium smegmatis was investi

250 Sulfite reduction is one such mycobacterium-specific ste

251 orarchaeota, whereas genes for dissimilatory sulfite reduction were horizontally transferred to the K

252 ic acid cycle, NAD biosynthesis, nitrate and sulfite reduction, and CO2/CO fixation.

253 was due to deficient expression of fprA and sulfite reduction.

254 in the human gut is anaerobic respiration of sulfite released from the abundant dietary and host-deri

255 rence plants lacking SO activity accumulated sulfite, resulting in leaf damage and mortality.

256 ite application induced up-regulation of the sulfite scavenger activities in dark-stressed or unstres

257 denosine-5'-phosphosulfate reductase and the sulfite scavengers sulfite oxidase (SO), sulfite reducta

258 od for measuring APR activity by using novel sulfite-selective colorimetric or "off-on" fluorescent l

259 The sulfite-sensitive mutants accumulate applied sulfite and

260 tion, sulfide serves as the sulfur donor and sulfite serves as the acceptor, forming thiosulfate.

261 Ultraviolet photochemical reaction of sulfite (SO(3)(2-)) photosensitizer generates strongly r

262 to the wasteful and toxic byproducts CSA and sulfite (SO(3)(2-)), and depletion of cellular NADPH.

263 produce GSSH; PDO oxidises GSSH to sulfite; sulfite spontaneously reacts with polysulfides to genera

264 as a result of these mutations; however, the sulfite-stimulated activity decreased by more than 60%.

265 e, in a single analytical run, delta(34)S in sulfite, sulfate and thiosulfate in water samples by liq

266 consequence of SiR impairment, the levels of sulfite, sulfate, and thiosulfate were higher and glutat

267 ase is capable of being regenerated from its sulfite/sulfate heat stable salt, which enables the simu

268 ed by borates, sodium, thiosulfate, sulfate, sulfite, sulfide, bicarbonate, and other macromolecule-s

269 lfite radicals generated by the reactions of sulfite (sulfite anions or bisulfite anions) with holes

270 thione to produce GSSH; PDO oxidises GSSH to sulfite; sulfite spontaneously reacts with polysulfides

271 that in the C185S variant, in the absence of sulfite, the active site residue Tyr322 became disordere

272 Similarly, if chloride is added before sulfite, the lpH species is formed instead of the blocke

273 185S variant crystallized in the presence of sulfite, the Tyr322 residue relocalized to the active si

274 was observed in the presence of graphite and sulfite, thiosulfate, or polysulfides.

275 its reaction with ortho-phthaldialdehyde and sulfite to form isoindol-1-sulfonate.

276 animals, SO catalyzes the oxidation of toxic sulfite to sulfate as the final step in the catabolism o

277 ite oxidases are metalloenzymes that oxidize sulfite to sulfate at a molybdenum active site.

278 enzyme that catalyzes the oxidation of toxic sulfite to sulfate.

279 s the physiologically critical conversion of sulfite to sulfate.

280 that catalyze the six-electron reduction of sulfite to sulfide and nitrite to ammonia.

281 mmission 1.8.7.1) catalyzes the reduction of sulfite to sulfide in the reductive sulfate assimilation

282 that catalyzes the six-electron reduction of sulfite to sulfide.

283 ve pathway, which catalyzes the reduction of sulfite to sulfide.

284 tase catalyzes the six-electron reduction of sulfite to sulfide.

285 The method is based on the conversion of sulfite to volatile sulfur dioxide by acidification of t

286 ts that overexpress SiR are more tolerant to sulfite toxicity, exhibiting little or no damage.

287 These results indicate that while UV-sulfite treatment can be effective for treating PFOS and

288 are not mutually exclusive: (a) that sodium sulfite treatment disrupts critical virion-host protein

289 es, some of which were lost following sodium sulfite treatment.

290 CsoR is unreactive toward sulfite under the same conditions.

291 good correlation (r=0.99) between red wines sulfite value by standard DTNB (5,5'-dithio-bis-(2-nitro

292 The kcat/Km,sulfite values for the variants in the sulfur transfer r

293 Here, UV-sulfite was applied to a diluted AFFF to characterize e(

294 ssumed that the reaction of formaldehyde and sulfite was the only atmospheric source of HMS.

295 in the sulfur transfer reaction from GSSH to sulfite were 1.6- (Asp-102) and 4-fold (Ala-285) lower t

296 a more convoluted route that would result if sulfite were the primary acceptor of sulfane sulfur.

297 Succinate and sulfite were verified as the final reaction products.

298 ediated adsorption process and forms surface sulfite, which is subsequently oxidized into surface-SO(

299 ted the effects of both conventional and low sulfite wines on ex vivo human erythrocytes under oxidat

300 r artifact-free determination of sulfate and sulfite with consistent results for chloride when compar