2002
Carbonic Anhydrase in Mineralization of the Crayfish Cuticle
Abstract: The cuticle of the freshwater cray sh, Procambarus clarkii (Girard, 1852), has several extracellular, cuticular isozymes for carbonic anhydrase (CA) which were isolated and puri ed via af nity chromatography. To denature proteins not entombed in cuticle calcite the ground cuticle was washed twice with both a 0.5% SDS and 1.5% sodium hypochlorite solution prior to CA isolation. Total water soluble protein (WSP) was 133 § 68 (SD) mg/100 g (6) cuticle, whereas af nity column bound protein, CA, was 191 § 108 (SD) …
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“…Calcification following ecdysis requires the uptake of calcium from the medium as well as remobilization from storage organs, followed by transport in the hemolymph to the sites of calcification. Several workers [43,44] have suggested that cuticular epidermal CA possibly functions in maximizing the supply of carbonate ions from respiratory CO 2 by increasing the bicarbonate formation rate at the extracellular site of mineralization. In this regard, based on the CA activity pattern in the epidermal tissues during the molting cycle, it is possible that CA may play a role in calcification via providing the counterions HCO 3 -and H ?…”
Section: Discussion
mentioning
confidence: 99%