Active multifunctional

Normally, acetyl-CoA carboxylase exists in the cytosol as an inactive protomer, Mr = 2 x 105. Citrate induces polymerization of the protomer into long filaments of an active, multifunctional enzyme, Mr = 4.8 x 106. The... 

The CNP of natural cellulose are the basis for a new family of smart nanoremedies used for care and cure. For example, an experimental nanocream with optimal pH = 5 containing about 5% active multifunctional cellulose nanoparticles has demonstrated excellent texture, selective and gentle mechanical peeling. 

Bedworth and Tour [41] have synthesized a chiral oligomer 41 from the polymerization of an optically active multifunctional 1,T-binaphthyl monomer 42... 

Unfortunately, the use of light alkanes also presents some drawbacks. Indeed, they are less reactive, and more reaction steps are intrinsically involved in their reactions than for olefins, so that it is necessary to design catalysts which are more active, multifunctional, and selective enough to avoid over-oxidation of the desired products, since the latter are usually more reactive than the starting alkane. 

Dissymmetric systems shows exciton splitting of dichroic absorptions and optical activity and photochromic materials having NLO, photoresponsiveness and photorefractivity properties, which occurred due to the presence of azoaromatic and chiral functionalities in the polymers [62]. Finally, novel optically active multifunctional methacrylic copolymers were synthesized, which contained side-chains chiral moieties and linked to a photoconductive carbazolic and to a photochromic azoaromatic chromophores... 

In animals, acetyl-CoA carboxylase (ACC) is a filamentous polymer (4 to 8 X 10 D) composed of 230-kD protomers. Each of these subunits contains the biotin carboxyl carrier moiety, biotin carboxylase, and transcarboxylase activities, as well as allosteric regulatory sites. Animal ACC is thus a multifunctional protein. The polymeric form is active, but the 230-kD protomers are inactive. The activity of ACC is thus dependent upon the position of the equilibrium between these two forms ... 

FIGURE 25.9 Fatty add synthase in animals contains all the functional groups and enzyme activities on a single multifunctional subunit. The active enzyme Is a head-to-tall dimer of Identical subunits. (Adapted from Wakit, S. J., Stoops,... 

An alkene activated by an electron-withdrawing group—often an acrylic ester 2 is used—can react with an aldehyde or ketone 1 in the presence of catalytic amounts of a tertiary amine, to yield an a-hydroxyalkylated product. This reaction, known as the Baylis-Hillman reaction, leads to the formation of useful multifunctional products, e.g. o -methylene-/3-hydroxy carbonyl compounds 3 with a chiral carbon center and various options for consecutive reactions. 

Sirolimus (SRL), also termed rapamycin is a macrolide lactone isolated from the ascomycete species Stre-ptomyces hygroscopicus. After binding to its cytosolic receptor FKBP-12 the resulting complex inhibits the multifunctional serine-threonine kinase mTOR (mammalian target of rapamycin). Inhibition of mTOR prevents activation of the p70S6 kinase and successive... 

A type of waterside maintenance chemical treatment. Any of a very wide range of chemicals that prevent or reduce tendencies of deposition, fouling, scaling, corrosion, or other unwanted phenomena to occur in a water system. Typically for smaller boiler plants, individual inhibitors are blended together to produce various multifunctional formulations specific for particular water chemistry and/or operating conditions. Larger boiler plants tend to use individual active component inhibitors. 

A-l,3-dimethylbutyl-A -phenyl quinone diimine (6QD1) has been introduced as a multifunctional additive for diene rubbers and provides an advantage in mixing characteristics (functions as peptizer and improves scorch safety) as well as improved performance (better antioxidant activity than paraphenylenediamine antidegradants) of the end products [36]. 

Two significant communications indicate the considerable potential of transition metal complexes as multifunctional homogeneous catalysts in the silane field (5, 53). Here the same catalyst activates silanes toward different substrates and it is probable that all proceed via a common metal hydrido intermediate. Both Co2(CO)8 and (Ph3P)3CoHX [X = H2, N2, or (H)Si(OEt)j] catalyze 0-silylation and hydrosilylation the hydrogen on Si may be replaced by R O, R COO, R CONH, or R3SiO [e.g., Eqs. (117)-(120)], and excellent yields of silylated product result. Phenolic groups do... 

In prokaryotes, each reaction of Figure 34-2 is catalyzed by a different polypeptide. By contrast, in eukaryotes, the enzymes are polypeptides with multiple catalytic activities whose adjacent catalytic sites facilitate channeling of intermediates between sites. Three distinct multifunctional enzymes catalyze reactions 3, 4, and 6, reactions 7 and 8, and reactions 10 and 11 of Figure 34-2. 

Five of the first six enzyme activities of pyrimidine biosynthesis reside on multifunctional polypeptides. One such polypeptide catalyzes the first three reactions of Figure 34-2 and ensures efficient channeling of carbamoyl phosphate to pyrimidine biosynthesis. A second bifunctional enzyme catalyzes reactions 5 and 6. 

To control the formation of nanoparticles with desired size, composition, structure, dispersion, and stability, a multifunction nanoagent is used. The active metals (Pd and Pt) react with the functional groups of the nanoagent, i.e., a pol5mier template. The polymer template determines the size, monodisperity, composition, and morphology of the particles (which is somewhat reminiscent of the reversed micelles technique mentioned above). 

Three factors determine the effectiveness of antioxidants in polymers, namely (i) intrinsic molar activity (ii) substantivity in the polymer and (iii) solubility in the polymer. Multifunctional AOs combine multiple functions in one molecule. Sterically hindered amine stabilisers (HAS), such as Chimassorb 944, Tinuvin 622 and Tinuvin 783 are prime examples. 

The preparation of imidazolides by acylation of imidazole with acid chlorides is sometimes limited by the inaccessibility or instability of the required acid chlorides (e.g., formyl chloride, highly unsaturated acid chlorides, etc.) or by side-reactions in the case of multifunctional systems. For these reasons and due to the availability of an easy and convenient procedure involving very mild conditions, imidazolides today are usually prepared directly from the corresponding carboxylic acids with jV -carbonyldiimida-zole (CDI) or one of its analoga (see page 16). Use of these reagents has become more and more the preferred method for activation of carboxylic acids to azolides and their further transacylation to esters, amides, peptides, etc. (see subsequent Chapters). 

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