BACKGROUND Wine yeasts can produce undesirable sulfur compounds during alcoholic fermentation, such as SO2 and H2S, in variable amounts depending mostly on the yeast strain but also on the conditions. However, although sulfur metabolism has been widely studied, some of the genetic determinants of differences in sulfite and/or sulfide production between wine yeast strains remain to be identified...

BACKGROUND Recent advances in the development of enzyme cocktails for degradation of lignocellulosic biomass, especially the discovery of lytic polysaccharide monooxygenases (LPMOs), have opened new perspectives for process design and optimization. Softwood biomass is an abundant resource in many parts of the world, including Scandinavia, but efficient pretreatment and subsequent enzymatic hydr...

The aerobic oxidation of sulfite thus provides a magnified manometric response to the chain initiating event. Advantage was taken of this circumstance to develop an ultrasensitive assay for milk xanthine oxidase (5). The data obtained were consistent with the hypothesis that xanthine oxidase, when acting on purine substrates, initiates the aerobic oxidation of sulfite by the generation of free ...

The molybdenum-containing enzyme sulfite oxidase catalyzes the conversion of sulfite to sulfate, the terminal step in the oxidative degradation of cysteine and methionine. Deficiency of this enzyme in humans usually leads to major neurological abnormalities and early death. The crystal structure of chicken liver sulfite oxidase at 1.9 A resolution reveals that each monomer of the dimeric enzyme...

Extracts of representative bacterial strains from the various families of photosynthetic prokaryotes are demonstrated to possess significant levels of sulfite reductase [EC 1.8.99.1; hydrogen-sulfide: (acceptor)oxidoreductase] activity with reduced methyl viologen as electron donor, but not NADPH(2). The enzyme is localized primarily in the soluble fraction of the extracts, in contrast to adeny...

Previous papers in this series have reported the hypoxanthinedependent oxidation of sulfite by cyanide-inhibited xanthine oxidase (1) and experiments which permitted postulation of the structure of the active site of this enzyme (2). In the present study, xanthine oxidase acting on its substrates has been found to initiate the aerobic oxidation of sulfite by free radical chains of great length ...

We studied the kinetics of reactions of cob(I)alamin and cob(I)inamide with thiosulfate, sulfite, and dithionite by UV-Visible (UV-Vis) and stopped-flow spectroscopy. We found that the two Co(I) species were oxidized by these sulfur-containing compounds to Co(II) forms: oxidation by excess thiosulfate leads to penta-coordinate complexes and oxidation by excess sulfite or dithionite leads to hex...

A reduced nicotinamide adenine dinucleotide phosphate (NADPH)-specific enzyme from Escherichiu wti, isolated as a nitrite reductase, catalyzed the reductions of both nitrite and hydroxylamine to ammonia, and the ratio of the two activities remained constant during partial purification (1). The demonstration in the same species of an NADPH-specific enzyme catalyzing the reductions of hydroxylami...

Transposon Tn5 insertions causing anaerobic cysteine auxotrophy were isolated from a Salmonella typhimurium cysI parent (auxotrophic under aerobic but not anaerobic conditions). Insertions in one mutant group appeared to be in cysG. A second group of insertions, designated asr (anaerobic sulfite reduction), were located near map unit 53 on the S. typhimurium chromosome. They did not cause aerob...

An enzyme electrode was developed using the enzyme sulfite oxidase (EC1.8.3.1) immobilized onto pig intestine. Hydrogen peroxide produced was monitored amperometrically. All experimental parameters such as pH, temperature, buffer constituent concentration, were thoroughly investigated and optimized when appropriate. The response to sulfite concentration was linear in the range 5.2´...