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Plant Physiol, October 2000, Vol. 124, pp. 681-692

Stearoyl-Acyl Carrier Protein and Unusual Acyl-Acyl Carrier Protein Desaturase Activities Are Differentially Influenced by Ferredoxin1

David J. Schultz, Mi Chung Suh,2 and John B. Ohlrogge*

Department of Botany and Plant Pathology, Michigan State University, East Lansing, Michigan 48824

Acyl-acyl carrier protein (ACP) desaturases function to position a single double bond into an acyl-ACP substrate and are best represented by the ubiquitous Delta 9 18:0-ACP desaturase. Several variant acyl-ACP desaturases have also been identified from species that produce unusual monoenoic fatty acids. All known acyl-ACP desaturase enzymes use ferredoxin as the electron-donating cofactor, and in almost all previous studies the photosynthetic form of ferredoxin rather than the non-photosynthetic form has been used to assess activity. We have examined the influence of different forms of ferredoxin on acyl-ACP desaturases. Using combinations of in vitro acyl-ACP desaturase assays and [14C]malonyl-coenzyme A labeling studies, we have determined that heterotrophic ferredoxin isoforms support up to 20-fold higher unusual acyl-ACP desaturase activity in coriander (Coriandrum sativum), Thunbergia alata, and garden geranium (Pelargonium × hortorum) when compared with photosynthetic ferredoxin isoforms. Heterotrophic ferredoxin also increases activity of the ubiquitous Delta 9 18:0-ACP desaturase 1.5- to 3.0-fold in both seed and leaf extracts. These results suggest that ferredoxin isoforms may specifically interact with acyl-ACP desaturases to achieve optimal enzyme activity and that heterotrophic isoforms of ferredoxin may be the in vivo electron donor for this reaction.


1 This work was supported in part by the Michigan Soybean Promotion Board and the U.S. Department of Agriculture, National Research Initiative (grant no. 98-35505-6190) and by the Michigan Agricultural Experiment Station.

2 Present address: Plant Cell Biotechnology Laboratory, Korea Research Institute of Biosciences and Biotechnology, P.O. Box 115, Yusong Taejon, 305-600, Korea.

* Corresponding author; e-mail ohlrogge{at}pilot.msu.edu; fax 517-353-1926.

© 2000 American Society of Plant Physiologists



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