By F. F. (Editor); Nord
Advances in Enzymology and similar parts of Molecular Biology is a seminal sequence within the box of biochemistry, supplying researchers entry to authoritative reports of the most recent discoveries in all components of enzymology and molecular biology. those landmark volumes date again to 1941, offering an unequalled view of the historic improvement of enzymology. The sequence deals researchers the most recent realizing of enzymes, their mechanisms, reactions and evolution, roles in advanced organic technique, and their software in either the laboratory and undefined. every one quantity within the sequence good points contributions by way of prime pioneers and investigators within the box from all over the world. All articles are rigorously edited to make sure thoroughness, caliber, and clarity.
With its wide selection of themes and lengthy ancient pedigree, Advances in Enzymology and similar parts of Molecular Biology can be utilized not just by way of scholars and researchers in molecular biology, biochemistry, and enzymology, but additionally via any scientist drawn to the invention of an enzyme, its homes, and its purposes.
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Additional info for Advances in Enzymology and Related Areas of Molecular Biology, Volume 31
The growth effect is elicited both in vitro and in vivo. When embryonic sensory or sympathetic ganglia are explanted and cultured in synthetic medium, the addition of minute amounts of NGF (10-’M) brings about a striking nerve fiber outgrowth, already apparent as a dense halo after a few hours of incubation (22,39). , in mice) may reach a volume up to ten times that of respective normal controls (30,35). Conversely, an antiserum prepared against a purified NGF preparation, when injected into newborn animals brings about the almost complete destruction of the sympathetic nervous system (13,36).
Model of acid DNase. From Monod et al. (140). which is in agreement with the model postulated by Monod, Wyman, and Changeux (140). As already mentioned, single-stranded DNA’s are much poorer substrates and single-stranded polyribonucleotides are much poorer inhibitors than their double-stranded, antiparallel, counterparts. In conclusion, a schematic model of the acid DNase molecule may be that of Figure 24, which is taken from the paper of Monod, Wyman, and Changeux (140). In connection with this model, it may be relevant to recall that the dimer of &lactoglobulin, which has a molecular weight, 36,000, very close to that of acid DNase, has a distance between the two centers of the monomer units equal to 18 b, as determined by x-ray crystallography (141,142).
0 (135-137), do not inhibit, whereas those which have anti-parallel, double-stranded structures 39 ACID DEOXYRIBONUCLEASE I vs i Fig. 20. Competitive inhibition of hog spleen acid DNase by yeast tRNA. The number in parentheses indicate the mpmoles of tRNAP/ml. u = pmoles DNA-P liberated in 15 min, s = pmoles DNA-P/ml. From Bernardi (132). like poly A-poly U and poly I-poly C, or regions with this type of structure, like tRNA and ribosomal RNA do inhibit acid DNase (138,139). It seems, therefore, that structures simulating that of native DNA are endowed with the highest affinity for the enzyme.
Advances in Enzymology and Related Areas of Molecular Biology, Volume 31 by F. F. (Editor); Nord