Dithiothreitol, reaction

The reaction of OH with thiolate ions, taken as an overall reaction, is an ET reaction [reaction (36)]. One must, however, again take into account that a three-electron bonded intermediate is formed in the first step (Chap. 7). In semi-de-protonated dithiothreitol reaction (32) dominates over the H-abstraction reaction (33) (Akhlaq and von Sonntag 1987), although the rate constant for the reaction of OH with a thiol and a thiolate ion are both diffusion controlled (k = 1.5 x 1010 dm3 mol-1 s 1). This is another example of the potentially high regio-selectivity of OH reactions. 

Ascorbic acid and dehydroascorbic acid have been determined by reversed-phase h.p.l.c., post-column reduction of dehydroascorbic acid to ascorbic acid with dithiothreitol, reaction of excess reagent with JV-ethylmaleimide, and electrochemical detection. Ascorbic acid and its 2-phosphate were determined by h.p.l.c. on an aminopropyl bonded-phase silica column. Dehydroascorbic acid could also be determined by the increase in the ascorbic acid content after reduction with dithiothreitol The method was applied to raw apple and potato to which these compounds are added to prevent browning. ... 

FIGURE 5.18 Methods for cleavage of disulfide bonds in proteins, (a) Oxidative cleavage by reaction with performic acid, (b) Reductive cleavage with snlfliydryl compounds. Disulfide bridges can be broken by reduction of the S—S link with snlfliydryl agents such as 2-mercaptoethanol or dithiothreitol. Because reaction between the newly reduced —SH groups to re-establish disulfide bonds is a likelihood, S—S reduction must be followed by —SH modification (1) alkylation with iodoac-etate (ICH,COOH) or (2) modification with 3-bromopropylamine (Br— (CH,)3—NH,). 

There are other substrates for the E. coli Met(0) peptide reductase, one of which is Met(0)-a-l-PI. The native protein is the major serum elastase inhibitor that functions by forming a binary complex with elastase which inhibits its activity. Met(0)-a-l-PI, on the other hand, which can be formed by treatment of the protein with TV-chlorosuccinimide, cannot form a complex with elastase and therefore is not able to inhibit elastase activity117,118. Table 6 shows, however, that when Met(0)-a-l-PI is incubated in the presence of Met(0)-peptide reductase and dithiothreitol the protein regains its ability to form a complex with elastase and inhibit elastase activity119. Similar to results found with Met(0)-L12 reduced thioredoxin could replace the dithiothreitol as reductant in the enzymatic reaction. 

The reduction of ribonucleoside triphosphates by various dithiols which are capable of intramolecular cyclization on oxidation (dihydrolipoate, dithioerythritol, dithiothreitol) yields 2 -deoxyribonucleoside triphosphates. These reactions also require 5-deoxyadenosylcorrinoids. 

In an analogous reaction catalyzed by 2,5-dihydroxypyridine 5,6-dioxygenases from various strains (Scheme 3d), the hydrolysis products maleamate and formate were identified. The latter enzymes require Fe2+ and a thiol donor such as dithiothreitol, cysteine, or glutathion for activity. 

The following protocol for labeling proteins with 5-IAF is adapted from Gorman (1987). It is a bit unusual in that it involves reduction of disulfides with dithiothreitol (DTT) and immediate reaction with 5-IAF in excess without removal of excess reductant. The procedure can be changed to include a gel filtration step after disulfide reduction to remove excess DTT, but in any case, it should be optimized for each protein to be modified. An alternative to the use of DTT to produce sulfhydryls is thiolation with a compound that can generate free thiols upon reaction with a protein (Chapter 1, Section 4.1). 

Wash particles (e.g., 100 mg of 1 pm carboxylated latex beads) into coupling buffer (i.e., 50 mM MES, pH 6.0 or 50 mM sodium phosphate, pH 7.2 buffers with pH values from pH 4.5 -7.5 may be used with success however, as the pH increases the reaction rate will decrease). Suspend the particles in 5 ml coupling buffer. The addition of a dilute detergent solution may be done to increase particle stability (e.g., final concentration of 0.01 percent sodium dodecyl sulfate (SDS)). Avoid the addition of any components containing carboxylates or amines (such as acetate, glycine, Tris, imidazole, etc.). Also, avoid the presence of thiols (e.g., dithiothreitol (DTT), 2-mercaptoethanol, etc.), as these will react with EDC and effectively inactivate it. 

The recent work by Winterbourn and Metodiewa [211] demonstrated that the above values for the rate constant of reaction of DHLA with superoxide might be overestimated. These authors studied the reactions of superoxide with several thiols, glutathione, cysteine, cysteamine, penicillamine, /V-acetylcysteine, dithiothreitol, and captopril and found that thiols reacted with superoxide by a chain mechanism with the regeneration of superoxide. They suggested that the rate constants for the reactions of thiols with superoxide could not be more than 103 ImoN1 s-1. 

Von Sonntag and coworkers14 repeated Michael and Hart s study of the reaction of OH radical with 1,3- and 1,4-cyclohexadienes and extended it. They found that in the case of 1,4-cyclohexadiene, 50% of the OH radicals abstract an hydrogen atom, while only about 25% of the OH radicals abstract an hydrogen atom from 1,3-cyclohexadiene. The remaining OH radicals probably add to the double bond. The addition to the double bond was confirmed by final products analysis in the case of the 1,4-isomer. When N20-saturated aqueous solution of 1,4-cyclohexadiene (10-2 M) together with lower (10-4 M) concentration of the thiol (1,4-dithiothreitol) was y-radiolysed, it was found that 4-hydroxycyclohexene was produced with a yield of 0.29 prnol J 1, i.e. a yield of 50% of the OH radicals (equation 9). 

The activation of H2 photoproduction by CaCl2 was observed not only with Tris buffer as an electron donor but with sucrose, dithiothreitol, or methanol as well. BaCl2, like CaCl2, enhanced the rate of H2 photoproduction by a factor of about 30. Chlorides of monovalent metals increased the reaction rate in the system Tris-Ti02-hydrogenase insignificantly [2],... 

List of Abbreviations PCR, polymerase chain reaction RT-PCR, reverse transcription polymerase chain reaction DNA, deoxyribonucleic acid RNA, ribonucleic acid RNase, ribonuclease mRNA, messenger RNA GABAa, y-aminobutyric acid type A cRNA, copy RNA dNTPs, deoxy nucleoside triphosphates MMLV, Mouse Moloney murine leukemia vims RT, reverse transcriptase bp, base pair Tm, melting temperature DEPC, diethylpyrocarbonate OD, optical density mL, milliliter SA-PMPs, streptavidin paramagnetic particles dT, deoxy thymidine DTT, dithiothreitol DNase, deoxyribonuclease RNasin, ribonuclease inhibitor UV, ultraviolet TBE, Tris-borate, 1 mM EDTA EDTA, ethylenediaminetetraacetic acid Buffer RET, guanidium thiocyanate lysis buffer PBS, phosphate buffered saline NT2, Ntera 2 neural progenitor cells... 

Dithiothreitol can be used as the source of electrons for the reaction in vitro, although it is widely held that the reduction of the GR in vivo is linked to the pool of reduced nucleotides (NADH or NADPH). A more detailed description of the characterization of each component of the GR is given below. 

This enzyme [EC 1.8.4.5], also known as methionine S-oxide reductase, catalyzes the reaction of L-methionine with oxidized thioredoxin to produce L-methionine S-oxide and reduced thioredoxin. Dithiothreitol can substitute for reduced thioredoxin in the reverse reaction. In addition, other methyl sulfoxides can replace methionine sulfoxide in the reverse reaction. 

This pyridoxal-phosphate-dependent enzyme [EC 4.4.1.16], also known as selenocysteine reductase, catalyzes the reaction of L-selenocysteine with a reduced acceptor to produce hydrogen selenide, L-alanine, and the acceptor. The enzyme can use dithiothreitol or 2-mercaptoethanol as the reducing agent. Cysteine, serine, or chloroalanine are not alternative substrates for this enzyme. 

I. 1.4.1] catalyzes the reaction of 2-methyl-3-phytyl-l,4-naphthoquinone with oxidized dithiothreitol and water to produce 2,3-epoxy-2,3-dihydro-2-methyl-3-phytyl-l,4-naphthoquinone and 1,4-dithiothreitol. In the reverse reaction, vitamin K 2,3-epoxide is reduced to vitamin K and possibly to vitamin K hydroquinone by 1,4-dithioer-ythritol (which is oxidized to the disulfide). Some other dithiols and butane-4-thiol can also act as substrates. This enzyme is strongly inhibited by warfarin. 

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