Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Residue incorporated

Donor Residue Incorporated Into Growth Medium of Receiver. Because plant litter, In addition to root exudates, Is a potential source of allelochemicals (17), several studies have Investigated the Influence of residues of plants on mineral absorption by receivers. Two extensive studies have been done by Bhowmik and Doll (18, 19). [Pg.164]

Residues incorporated or Dandelion Taraxacum officinale L. Weber, perennial on the soil surface sowthistle Sonchus arvensis L., kochia Kochia... [Pg.390]

With the C-terminal residue introduced as part of the BAL anchor and the penultimate residue incorporated successfully by the optimized acylation conditions just described, further stepwise chain elongation by addition of Fmoc-amino acids generally proceeded normally by any of a variety of peptide synthesis protocols. [Pg.136]

The amount of organic matter added. This is highly variable across rice production systems, depending on such factors as the time available between crops, mechanization allowing residue incorporation, alternative requirements for organic matter, and so forth. Often straw is entirely removed from the... [Pg.236]

Method a. (ji-Styryl) phenyl telluride. To a solution of methyltriphenylphosphonium iodide (0.405 g, 1 mmol) in dry THF (4 mL) at room temperature was added dropwise n-BuLi (2 mmol). After stirring at room temperature for 20 min the solution was cooled to -78°C and a solution of PhTeBr (0.28 g, 1 mmol in 2 mL THF) was added, followed by benzaldehyde (0.16 g, 1.5 mmol). The temperature was raised to room temperature and stirred for 3 h. The solvent was removed under vacuum and the residue incorporated on Si02 and purified by flash column chromatography (Si02/hexane) giving an oil. Yield 0.185 g (60%). E/Z=2. [Pg.92]

Laux Process. This is a modification of the Bechamp process for the iron reduction of nitrobenzene to aniline which leaves iron oxide as the residue. Incorporation of iron or aluminium chlorides into the reduction process produces high quality yellow and red iron oxide pigments... [Pg.126]

S ATP -I- muscarinic cholinergic receptor <3> (<3> from chick heart [7-9] <3> in vitro as good as -adrenergic receptor, phosphorylation depends on the presence of a muscarinic agonist ligand, not merely receptor occupancy, the agonist induces a conformational change, which allows phosphorylation, phosphorylation sites 70% Ser- and 30% Thr-residues, incorporation of 3-4 mol phosphate/mol receptor [7]) (Reversibility <3> [7-9]) [7-9]... [Pg.93]

Several monosaccharides mentioned in this Section are present in polysaccharide chains not only as pyranoses but also as furanoses. From the biogenetic point of view, a furanosidic form of a monosaccharide must be considered to be an additional component, as no ready interconversions of cyclic forms may be expected for monosaccharide residues incorporated into oligosaccharide chains, or in the activated form used for their formation. [Pg.298]

Fig. 1.1b., the use of a-[32P] dGTP as the labelled substrate results in the incorporation of a radioactive label in the phosphodiester band to the 5 -side of all guanosine residues incorporated. [Pg.10]

More recently, MPO-mediated oxidation of tyrosine to dityrosine (o o -dityrosine, or 3,3 -diiyrosine) focused attention as a marker reaction of neutrophile-dependent oxidative damage of proteins and peptides (G11, H14, S3). The reaction occurs both with free tyrosine as well as with tyrosyl residues incorporated into polypeptide structures. The mechanism of dityrosine formation utilizes a relatively long-lived phenoxyl radical that cross-links to dimeric and polymeric structures by formation of carbon-carbon bonds between the aromatic moieties of phenolic tyrosine residues (H14) (Fig. 9). [Pg.178]

The effect of N-acetyl substitution in methionine on the nature of transients formed after one-electron oxidation was studied as a function of pH and NAM concentration. The observed absorption bands with X = 290 nm, 360 nm, and 490 nm were respectively assigned to a-(alkylthio)alkyl, hydroxysulfuranyl and dimeric radical cations with intermolecular three-electron bond between sulfur atoms. N-acetylmethionine amide (NAMA) (Chart 7) represents a simple chemical model for the methionine residue incorporated in a peptide. Pulse radiolysis studies coupled to time-resolved UV-Vis spectroscopy and conductivity detection of N-acetyl methionine amide delivered the first experimental evidence that a sulfur radical cation can associate with the oxygen of an amide function vide infra). ... [Pg.462]

To facilitate aminoacylation of A -(2-hydroxybenzyl)annino acids or -peptide derivatives via O—> N acyl migration various related nitro derivatives were proposed,among which the A -(2-hydroxy-6-nitrobenzyl) and A -(2-hydroxy-5-nitrobenzyl) proved significantly more reactive in this context than the Hmb anoino acid residues. Incorporation of these protecting groups is performed by reductive alkylation as for the Hmb derivatives and removal of the N -protecting group is readily achieved by mild photolysis at 366 nm for 3 hours. [Pg.265]

A methodology for the introduction of imidazole residues into DNA has been described by Min and Verdine. An 06-phenylinosine residue incorporated into... [Pg.205]

The glucuronic acid conjugation Is the most versatile of the conjugation reactions In terms of the range of xenobiotic substrates It may accept and Its widespread distribution through species and tissues. The glucuronic acid residue Incorporated Into the conjugate derives from the nucleotide uridine... [Pg.8]

Many intracellular proteins can be modified after their biosynthesis by the enzymatic addition of a methyl group from S-adenosylmethionine. These posttransla-tional reactions can permanently or temporarily modify the structure and function of the target proteins. Importantly, these modifications can expand the repertoire of the cellular chemistry performed by proteins. Unmodified proteins must function with only the 20 amino acid residues incorporated in ribosomal protein synthesis, while methylation reactions can create a variety of new types of residues for specialized cellular roles. At this point, we understand best the processes that reversibly form methyl esters at carboxylic acid residues. One such reaction in bacteria methylates glutamate residues on several membrane-bound chemorecep-tors whose signaling properties are modulated by the degree of modification at multiple methylation sites. Another methylation system in higher cells leads to C-terminal methyl ester formation on a variety of proteins such as the small and... [Pg.299]

The Family 3 structure is similar in structure to Family 1 pectate lyases, the pectate lyase of a Bacillus species being a parallel eight-turn (3-helix.Site-directed mutagenesis experiments supported a role for an arginine as the active site base that deprotonated C5, with a role for the second Ca " in stabilising the enolate (the first Ca " being structural). It is possible that the very existence of a Family 3 PL, separate from Family 1, is an artefact of the many basic residues incorporated into this enzyme that ensure its alkaline pFl optimum. [Pg.616]

Now, we are concerned with the Rn -.o values for Gly residue incorporated into (Ala) , (Leu) and (Val) as shown in Table 22.4. This table shows that the Rn...o value for the OR-helix form is in the range of 2.7-2.8 A and the /3-sheet form is 3.0 A. The Rn -.o value for the jS-sheet form agrees with that for homopolypeptides as mentioned above. Also, the Rn o values for aR are widely distributed to some extent these results are quite similar to those for homopolypeptides. Moreover, the average value is almost the same as that for the homopolypeptides. This indicates that the glycine residue is incorporated completely into the homopolypeptides with the aR-helix and 13-sheet forms. [Pg.838]


See other pages where Residue incorporated is mentioned: [Pg.46]    [Pg.59]    [Pg.547]    [Pg.101]    [Pg.163]    [Pg.157]    [Pg.389]    [Pg.412]    [Pg.265]    [Pg.377]    [Pg.383]    [Pg.132]    [Pg.414]    [Pg.616]    [Pg.32]    [Pg.125]    [Pg.45]    [Pg.203]    [Pg.285]    [Pg.54]    [Pg.261]    [Pg.87]    [Pg.10]    [Pg.87]    [Pg.203]    [Pg.2138]    [Pg.180]    [Pg.2221]    [Pg.98]    [Pg.838]    [Pg.846]    [Pg.133]    [Pg.544]   
See also in sourсe #XX -- [ Pg.253 ]




SEARCH



Biologically incorporated residues

© 2024 chempedia.info