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Control of Lipid Synthesis During Soybean Seed Development: Enzymic and Immunochemical Assay of Acyl Carrier Protein

Overview
Journal Plant Physiol
Specialty Physiology
Date 1984 Mar 1
PMID 16663471
Citations 16
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Abstract

During soybean seed (Glycine max, var Am Soy 71) development, the rate of lipid biosynthesis per seed increases greatly. As the seed reaches maturity, lipid synthesis declines. To study the controls over the oil synthesis and storage process, we have chosen acyl carrier protein (ACP) as a representative marker for the fatty acid synthetase pathway. We have quantitated soybean ACP levels by both enzymic and immunochemical methods. Escherichia coli acyl-ACP synthetase was used as an assay for enzymically active ACP. Total ACP protein was determined by immunoassay using antibodies prepared in rabbits against spinach ACP. These antibody preparations also bind ACP isolated from soybeans, allowing development of a radioimmunoassay based on competition with [(3)H]palmitoyl-ACP. The enzymic and immunochemical measurement of ACP at various stages of seed development have indicated that ACP activity and ACP antigen increase markedly in correlation with the in vivo increase in lipid synthesis. These results indicate that a major control over the increase in lipid synthesis arises through regulation of the levels of the fatty acid biosynthetic proteins. However, as the seed reaches maturity and lipid biosynthesis declines, ACP per seed remains relatively high. In the mature seed, we found that more than 95% of the ACP is localized in the cotyledons, less than 5% is in the axis, and less than 1% is in the seed coat.

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References
1.
Turnham E, Northcote D . Changes in the activity of acetyl-CoA carboxylase during rape-seed formation. Biochem J. 1983; 212(1):223-9. PMC: 1152033. DOI: 10.1042/bj2120223. View

2.
Porra R, Stumpf P . Lipid biosynthesis in developing and germinating soybean cotyledons. The formation of palmitate and stearate by chopped tissue and supernatant preparations. Arch Biochem Biophys. 1976; 176(1):53-62. DOI: 10.1016/0003-9861(76)90140-5. View

3.
Rock C, Cronan Jr J . Solubilization, purification, and salt activation of acyl-acyl carrier protein synthetase from Escherichia coli. J Biol Chem. 1979; 254(15):7116-22. View

4.
Simoni R, Criddle R, Stumpf P . Fat metabolism in higher plants. XXXI. Purification and properties of plant and bacterial acyl carrier proteins. J Biol Chem. 1967; 242(4):573-81. View

5.
Privett O, Dougherty K, Erdahl W, Stolyhwo A . Studies on the lipid composition of developing soybeans. J Am Oil Chem Soc. 1973; 50(12):516-20. DOI: 10.1007/BF02640523. View