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Abstract

For many years pharmacologists have been interested in biologically active proteins in snake venoms (Kaiser and Michel, 1958). Highly specific methods are often necessary in enzymatic studies, and enzymes from snake venoms are used in some of these methods. These enzymes include phospholipase A (EC 3.1.1.4), L-amino-acid oxidase (EC 1.4.3.2), phosphodiesterase (EC 3.1.4.1), and 5′-nucleotidase (EC 3.1.3.5). Much of the literature on these has been reviewed (Zeller, 1948, 1951; Van Heyningen, 1954; Slotta, 1955; Sarker and Devi, 1968). The availability of highly purified enzyme proteins has enabled rapid progress in the characterization of many enzymes and of their biological activity, so more up-to-date reviews are constantly required. Proteinase and arginine ester hydrolase activity have been found in the venoms of Crotalidae (Agkistrodon, Bothrops, Crotalus, Lachesis, and Trimeresurus species) and some venoms of Viperidae. The venoms of Elapidae usually do not contain proteinase or arginine ester hydrolase activity and thus they do not digest proteins, but they react strongly toward peptides of rather small molecular weight (Murata et al., 1963).

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Suzuki, T., Iwanaga, S. (1970). Snake Venoms. In: Erdös, E.G., Wilde, A.F. (eds) Bradykinin, Kallidin and Kallikrein. Handbook of Experimental Pharmacology / Handbuch der experimentellen Pharmakologie, vol 25 / 25. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-46222-1_9

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