11:15 AM - 11:30 AM
[BCG05-03] Carbonic anhydrase in Foraminifera: Perspective on one of major role of ‘vital effect’
Keywords:carbonic anhydrase, calcification, stable oxygen and carbon isotopes
Carbonic anhydrase (CA) and aquaporin 4 (AQP4) genes showed significant expression during calcification in the transcriptomics. The enzyme CA catalyzes the interconversion of H2O + CO2 to HCO3- + H+. The integral membrane protein AQP4 allows the passage of water molecules through the cell membrane and supplies H2O for further HCO3-production around the cell membrane. CO2 can be diffused from seawater as well as calcification sites and produced during metabolic processes. The CA and AQP4 expressions imply the intracellular generation of HCO3-. The phylogenetic analysis of CAs indicated that Rotaliida foraminifer has two out of five CA families: α-CA and b-CA members. α-CAs are involved in CO2/HCO3- interconversion and calcification in mollusks, sea urchins, and corals. In mollusks, calcification-related α-CAs contain acidic low-complexity regions (LCRs), which could bind Ca2+ leading to CaCO3 nucleation. While, Rotaliida’s α-CAs formed two clades, one of which (Rotaliida-αCA1) is a novel independent clade from metazoans and some has acidic LCRs. Rotaliida-αCA1 seems to catalyze CO2/HCO3- interconversion which is related to foraminiferal calcification. Moreover, our in silico protein motif predictions indicated that Rotaliida-αCA1 comprised both secretory α-CAs and intracellular α-CAs. The former is likely involved in HCO3- generation and calcium-binding at the extracellular calcification site. The latter does not interact with Ca2+ as they lack acidic LCRs; hence, they likely participate in HCO3- production in the cytosol. These different distributions of α-CA enable the utilization of CO2 derived from both extracellular and intracellular origins. The multiple sources, in particular those of CO2, serve as a physiological control mechanism for d18O and d13C in foraminiferal tests via HCO3- production. Such physiology could be partly responsible for the non-equilibrium state of d18O and d13C between foraminiferal tests and the environment observed in geochemical studies.