The archaeogastropod mollusc Haliotis iris: tissue and blood metabolites and allosteric regulation of haemocyanin function
Jane W. Behrens1,3,
John P. Elias2,3,
H. Harry Taylor3 and
Roy E. Weber1,*
1 Department of Zoophysiology, Institute Biological Sciences, University of Aarhus, DK 8000 Aarhus, Denmark,
2 School of Biological Sciences, Monash University, Clayton, Victoria 3800, Australia and
3 Department of Zoology, University of Canterbury, Private Bag 4800, Christchurch, New Zealand

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Fig. 1. The concentrations of tauropine (A) and D-lactate (B) in the haemolymph (AO, aorta; PS, pedal sinus; AH, adductor haemocoel; mmol l1) and the tissues (FM, foot muscle; AM, adductor muscle; mmol kg1 fresh mass) in Haliotis iris settled in water (open columns) or emersed in air for 24 h (filled columns) at 15°C. Values are means + S.E.M.; see Table 1 for N values.
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Fig. 2. The effects of dialysis against various ions on the O2-affinity (logP50) of Haliotis iris haemocyanin at 15°C, pH 7.0 (filled columns) and pH 7.7 (open columns). Labels above the columns refer to the concentrations (mmol l1) of Ca2+ (Ca), Mg2+ (Mg), D-lactate (D-l), and L-lactate (L-l). nh, native haemolymph; dHc, dialysed haemocyanin without added cofactor.
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Fig. 3. The effects of various ions on the cooperativity (n50) of Haliotis iris haemocyanin O2-binding at 15°C. Labels in the legend refer to the concentrations (mmol l1) of Ca2+ (Ca), Mg2+ (Mg), D-lactate (D-l), and L-lactate (L-l). nh, native haemolymph; dHc, dialysed Hc without added cofactor.
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Fig. 4. Hill plot for dialysed haemocyanin of Haliotis iris measured in the absence (circles) and in the presence (triangles) of 50 mmol l1 Mg2+, in 0.1 mol l1 Bis-Tris buffer at pH 7.7 and 15°C. KT and KR are estimates of O2 association equilibrium constants (mmHg1) for the low-affinity (T, tense) and high-affinity (R, relaxed) forms, respectively. S, fractional oxygen saturation.
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© The Company of Biologists Ltd 2002