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Plant Physiology 91:477-480 (1989) © 1989 American Society of Plant Biologists Inositol Trisphosphate Metabolism in Carrot (Daucus carota L.) Cells 1Department of Botany, Box 7612, North Carolina State University Raleigh, North Carolina 27695
The metabolism of exogenously added D-myo-[1-3H]inositol 1,4,5-trisphosphate (IP3) has been examined in microsomal membrane and soluble fractions of carrot (Daucus carota L.) cells grown in suspension culture. When [3H]IP3 was added to a microsomal membrane fraction, [3H]IP2 was the primary metabolite consisting of approximately 83% of the total recovered [3H] by paper electrophoresis. [3H]IP was only 6% of the [3H] recovered, and 10% of the [3H]IP3 was not further metabolized. In contrast, when [3H]IP3 was added to the soluble fraction, approximately equal amounts of [3H]IP2 and [3H]IP were recovered. Ca2+ (100 micromolar) tended to enhance IP3 dephosphorylation but inhibited the IP2 dephosphorylation in the soluble fraction by about 20%. MoO42 (1 millimolar) inhibited the dephosphorylation of IP3 by the microsomal fraction and the dephosphorylation of IP2 by the soluble fraction. MoO42, however, did not inhibit the dephosphorylation of IP3 by the soluble fraction. Li+ (10 and 50 millimolar) had no effect on IP3 metabolism in either the soluble or membrane fraction; however, Li+ (50 millimolar) inhibited IP2 dephosphorylation in the soluble fraction about 25%.
2 Permanent address: Department of Biology, Middle East Technical University, Ankara, Turkey. 3 Present address: Noble Foundation, P. O. Box 2180, Ardmore, OK 73402. 1 Supported by grant No. DE-FG05-87ER 13693 from the U.S. Department of Energy. Paper No. 12229 of the Journal Series of the North Carolina Agricultural Research Service, Raleigh, NC 27695-7601. This article has been cited by other articles:
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