Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: EC:1.13.12.5 (aequorin)
 1,451 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Histochemical analysis was used to study the relationship between Rana temporaria tibialis anterior and lumbricalis IV fibre cross-sectional areas and concentrations of myosin ATPase and NADH reductase. Both tonic and twitch fibre types were histochemically identified in each muscle and the twitch fibres were subgrouped into types 1, 2, and 3. Fibres that had the largest cross-sectional areas were identified as the fibres which contained the highest myosin ATPase activity and the lowest NADH reductase activity (type 1 fibres). However, this relationship was more pronounced in the tibialis anterior muscle. In addition, single fibres from both muscles were isolated and injected with Ca2+ indicator aequorin. The fibres isolated from the tibialis anterior muscle were those with the largest cross-sectional areas relative to other fibres within a given muscle. The force responses and Ca2+ transients recorded from this group of single fibres were found to be fairly uniform, which may suggest that a single type of fibre was isolated. In contrast, the physiological properties of isolated lumbricalis IV fibres were highly variable and thus represented more than one fibre type.
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PMID:Histochemical and physiological properties of Rana temporaria tibialis anterior and lumbricalis IV muscle fibres. 225 38

Few systematic studies have been devoted to investigating the role of Ca2+ as an intracellular messenger in prokaryotes. Here we report an investigation on the potential involvement of Ca2+ in signalling in Bacillus subtilis, a Gram-positive bacterium. Using aequorin, it is shown that B. subtilis cells tightly regulate intracellular Ca2+ levels. This homeostasis can be changed by an external stimulus such as hydrogen peroxide, pointing to a relationship between oxidative stress and Ca2+ signalling. Also, B. subtilis growth appears to be intimately linked to the presence of Ca2+, as normal growth can be immediately restored by adding Ca2+ to an almost non-growing culture in EGTA containing Luria broth medium. Addition of Fe2+ or Mn2+ also restores growth, but with 5-6 h delay, whereas Mg2+ did not have any effect. In addition, the expression of alkyl hydroperoxide reductase C (AhpC), which is strongly enhanced in bacteria grown in the presence of EGTA, also appears to be regulated by Ca2+. Finally, using 45Ca2+ overlay on membrane electrotransferred two-dimensional gels of B. subtilis, four putative Ca2+ binding proteins were found, including AhpC. Our results provide strong evidence for a regulatory role for Ca2+ in bacterial cells.
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PMID:Calcium signalling in Bacillus subtilis. 992 Apr 12