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Inverted DNA

Copper(I) tends towards a tetrahedral coordination geometry in complexes. With 2,2 -bipyr-idine as a chelate ligand a distorted tetrahedral coordination with almost orthogonal ligands results. 2,2 -Bipyridine oligomers with flexible 6,6 -links therefore form double helices with two 2,2 -bipyridine units per copper(I) ion (J. M. Lehn, 1987,1988). J. M. Lehn (1990 U. Koert, 1990) has also prepared such helicates with nucleosides, e.g., thymidine, covalently attached to suitable spacers to obtain water-soluble double helix complexes, so-called inverted DNA , with internal positive charges and external nucleic bases. Cooperative effects lead preferentially to two identical strands in these helicates when copper(I) ions are added to a mixture of two different homooligomers. [Pg.345]

The resolvase / invertase family and invertible DNA sequences. A second large family of recombinases act by cleaving a target DNA sequence hydrolytically leaving a free 3 -OH end (Eq. 27-14, step a). This free end then attacks a phosphodiester linkage in a second strand of DNA, cleaving that strand with an in-line nucleophilic displacement (step b). Active sites usually contain a characteristic cluster of aspartate and... [Pg.1572]

Microorganisms sometimes control the synthesis of surface proteins using segments of invertible DNA. The pathogenic bacterium Campylobacter fetus utilizes DNA rearrangements to allow one of a large family of surface layer (S-layer) proteins to be formed.597 The yeast FLP recombinase, mentioned in the preceding section, also inverts the sequence flanked by the 599-bp repeats.589... [Pg.1573]

Inversion of configuration (cf Epimerization) of alcohols (Mitsunobu reaction), 160-161, 286 of ally lie acetates with Pd, 27, 164 of allylpalladium with d-synthons, 27, 264 of alkyl halides or sulfonates by 1,3-dithiane anions, 22 by organylcuprates, 36 by tetracarbonylferrate<2 -X 46-47 in triorganylborane rearr., 37-38 of glycosides with free 2-OH by DAST, 272 of glycosyl halides, 271 of oxiranes by 1-alkync anions, 64, 204 by enolate type anions, 63-64 by internal alcoholate addition, 265 Inversion-esterification of alcohols, 160-161, 286 Inverted DNA , 345-346 Iodide, hydrogen porphyrin synthesis with, 255 Iodine = diiodine (Ij) ... [Pg.212]

Ouellette M, Hettema E, Wust D et al. Direct and inverted DNA tepeats associated with P-glycoprotein gene amplification in drug resistant Leishmania. EMBO J 1991 10 1009-1016. [Pg.6]

A method to invert DNA segments of the Bacillus subtilis 168 genome by recombination between two homologous sequences. Biosci. Biotechnol, Biochem., 60 (5), 773—778. [Pg.290]

Fig. 3. Example of cniciform formation from an inverted-repeat sequence of DNA which occurs in the plasmid ColEl. The bolded bases are paired with... Fig. 3. Example of cniciform formation from an inverted-repeat sequence of DNA which occurs in the plasmid ColEl. The bolded bases are paired with...
FIGURE 12.27 The formation of a cruciform structure from a paliudromic sequence within DNA. The self-complementary Inverted repeats can rearrange to form hydrogen-bonded cruciform loops. [Pg.378]

An essential step of NR action is the interaction of these receptors with the specific DNA sequence HREs. Indeed, HREs position the receptors, and the transcriptional complexes recruited by them, close to the target genes. HREs are bipartite elements that are composed of two hexameric core half-site motifs. These consensus nucleotide sequences form direct, indirect, or inverted repeats, which consist of two half-sites separated... [Pg.896]

Transposons are mobile DNA elements (sizes 2.5-23 kbp) that move from one place to another in the chromosome or onto extrachromosomal genetic elements within the same cell. They are flanked by inverted repeats at then-ends and encode among other proteins a transposase that is needed for the transposition process. Resistance genes in the transposon are often parts of integrons. These are structures that cany an integrase responsible for the insertion of the resistance gene cassettes into the integron. [Pg.1242]

Efforts were also made to invert the sense of enantioselectivity in the hydrolytic kinetic resolution of ester (1) using PAL with preferential formation of (R)-2 [40,411-Using epPCR and DNA shuffling, an (R)-selective mutant showing an E value of 30 was evolved by screening about 45 000 clones for the (R) enantiomer. The best mutant is characterized by 11 mutations, which are different from those of the best (S)-selective variant X [41]. [Pg.33]

This is an inverted parabolic relation in terms of ttx (calculated hydrophobic parameter of the substituents), which suggests that activity of these compounds first decreases as the hydrophobicity of substituents increases and after a certain point (inversion point ttx = 0.67), activity begins to increase. This may correspond to an allosteric reaction [54]. The indicator variable I is assigned the value of 1 and 0 for the presence and absence of N(CH3)2 substituent at the X position. Its positive coefficient suggests that the presence of a N(CH3)2 substituent at X position, increases the activity. REC is the relative effective concentration i.e., concentration relative to topotecan, whose value is arbitrarily assumed as 1, that is able to produce the same cleavage on the plasmid DNA in the presence of human topo I. [Pg.56]

FIG. 15 Cellular entry and intracellular kinetics of the cationic lipid-DNA complexes. Cationic lipid-DOPE liposomes form electrostatic complexes with DNA, and, in this case, also transferrin (Tf) is incorporated. Cellular uptake by endoc5dosis and endosomal acidification can be blocked with cytochaiasin B and bafilomycin Aj, respectively. DNA is proposed to be released at the level of endosomal wall after fusion of the carrier lipids with endosomal bilayer. This process is facilitated by the formation of inverted hexagonal DOPE phase as illustrated in the lower corner on the right. After its release to the C5doplasm DNA may enter the nucleus. (From Ref. 253. By permission of Nature Publishing Group.)... [Pg.831]

Figure 5.27 Bacteriophage Mu. (a) Genetic map of Mu. (Confusingly, there are two G s, the G gene and the invertible G segment. These are different G s.) (b) Integration of Mu into the host DNA, showing the generation of a five-base-pair duplication of host DNA. Figure 5.27 Bacteriophage Mu. (a) Genetic map of Mu. (Confusingly, there are two G s, the G gene and the invertible G segment. These are different G s.) (b) Integration of Mu into the host DNA, showing the generation of a five-base-pair duplication of host DNA.

See other pages where Inverted DNA is mentioned: [Pg.1572]    [Pg.1573]    [Pg.146]    [Pg.1505]    [Pg.659]    [Pg.660]    [Pg.660]    [Pg.638]    [Pg.639]    [Pg.639]    [Pg.317]    [Pg.1572]    [Pg.1573]    [Pg.146]    [Pg.1505]    [Pg.659]    [Pg.660]    [Pg.660]    [Pg.638]    [Pg.639]    [Pg.639]    [Pg.317]    [Pg.251]    [Pg.502]    [Pg.378]    [Pg.397]    [Pg.1302]    [Pg.433]    [Pg.897]    [Pg.939]    [Pg.459]    [Pg.470]    [Pg.471]    [Pg.184]    [Pg.323]    [Pg.832]    [Pg.838]    [Pg.159]    [Pg.370]    [Pg.157]    [Pg.89]   
See also in sourсe #XX -- [ Pg.146 ]




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