In Praise of Bees: A Cabinet of Curiosities by Elizabeth Birchall

By Elizabeth Birchall

EPUB eISBN: 9781846892042
Hardcover book: 2015
Electronic book: 2014

A entire research of the bee's position in human society from prehistoric cave work and inscribed clay drugs, via to our modern world

Covering every little thing concerning the relationships among human society and bees, this publication is stuffed with nuggets of bee technological know-how and functional beekeeping, delusion, faith, politics, philosophy, and folklore, plus a range of verse and a wealthy number of illustrations starting from medical etchings to fashionable photos. It additionally bargains an in-depth examine bees' advanced society and their current plight. the continued political and medical controversies relating to insecticides and different threats also are mentioned, given the bee's significance as plant pollinator in agriculture and the wild.

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Extra resources for In Praise of Bees: A Cabinet of Curiosities

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Other levels include the catalytic domain (recruitment and availability of substrate molecules, allosteric effectors, endogenous inhibitors, UDPase) as well as apparent CS compartmentation and trafficking of CS units to and integration into the plasma membrane. 1 EPHRAIM COHEN CHITIN SYNTHASE—EXPRESSION PATTERNS AND HORMONAL CONTROL Temporal CS expression, which fluctuates throughout insect development, is tissue specific and most likely depends on oscillatory levels of ecdysteroids. The beet armyworm, S.

1991), from integumental tissues of T. ni, H. cecropia (Cohen and Casida, 1982), C. , 1983) and CS enzyme extracted from whole pupae of S. , 1980a,b). , 1991). The difference in inhibition might be substantial as for example the IC50 values of polyoxin-D for L. cuprina, T. castaneum and S. 5 mM, 4 mM and 1 mM, respectively (Cohen, 1987a). The above discrepancies can be attributed to different crudeness of the various insect cell-free CS preparations (Cohen, 1987a). Compared with polyoxins, nikkomycins are more effective CS inhibitors, blocking chitin polymerization at low IC50 levels of 20 and 60 nM for T.

The best known, and the most extensively investigated inhibitor, is allosamidin (Fig. 9) isolated from mycelia of Streptomyces sp. , 1992). HN NH. C HC C O N H O N H NHCH3 HOOC CH N CH 3 HN O C. H2C CH N H COOH HC C O Argifin FIG. 9 Chemical structures of two microbially derived chitinase inhibitors, allosamidin and the cyclopentapeptide argifin. , 1986). , 2002). In contrast to most other chitinase sources, the insect and fungal enzymes were strongly inhibited by allosamidins with IC50 values at the nanomolar/micromolar range.

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