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Extra‐ and intra‐cellular carbonic anhydrase in relation to culture age in a high‐calcifying strain of Emiliania huxleyi Lohmann
Author(s) -
NIMER N. A.,
GUAN Q.,
MERRETT M. J.
Publication year - 1994
Publication title -
new phytologist
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.742
H-Index - 244
eISSN - 1469-8137
pISSN - 0028-646X
DOI - 10.1111/j.1469-8137.1994.tb02954.x
Subject(s) - carbonic anhydrase , emiliania huxleyi , biochemistry , nigericin , chloroplast , pyrenoid , bicarbonate , rubisco , biology , cytosol , photosynthesis , chemistry , enzyme , membrane , phytoplankton , nutrient , gene , endocrinology , ecology
SUMMARY The relationships between extra‐ and intra‐cellular carbonic anhydrase, calcification rate, utilization of dissolved inorganic carbon (DIG) and culture age were investigated in a high‐calcifying strain of Emiliania huxleyi. The detection of carbonic anhydrasc was dependent on culture age; neither the extra‐cellular activity of intact cells nor activity in crude homogenates was detected until the stationary phase. By the stationary phase DIC in the medium was totally depleted and the calcification rate had decreased by 60° 0 . Extra‐ and intra‐cellular carbonic anhydrase was stimulated by Na + but not Cl ions. The isolation of intact organelles by isopycnic gradient centrifugal ion from exponential and stationary phase cultures of high calcifying cells showed high carbonic anhydrase activity in the chloroplast fraction but carbonic anhydrase was not detected in low‐calcifying cells even after gradient centrifugation. Although 50/IM ethoxyzolamide was an effective inhibitor of carbonic anhydrase activity in vitro , photosynthetic 14 CO 2 fixation was only inhibited 30%, calcification rate 10%, and the internal inorganic carbon pool unaffected in intact cells. It is proposed that chloroplast carbonic anhydrase maintains the steady state flux of COj, from the chloroplast envelope to Rubisco, much of the CO 2 arising by release from HCO 3 − in the cytosol, required to maintain cytoplasmic pH near neutrality in high‐calcifying cells.