Molecular characterization of tobacco squalene synthase and regulation in response to fungal elicitor.
@article{Devarenne1998MolecularCO,
title={Molecular characterization of tobacco squalene synthase and regulation in response to fungal elicitor.},
author={Timothy P Devarenne and D. H. Shin and Kyoungwhan Back and Shaohui Yin and Joseph Chappell},
journal={Archives of biochemistry and biophysics},
year={1998},
volume={349 2},
pages={
205-15
}
}The enzyme squalene synthase (SS) represents the first commitment of carbon from the general isoprenoid pathway toward sterol biosynthesis and is a potential point for regulation of sterol biosynthesis. The isolation and characterization of tobacco (Nicotiana tabacum) squalene synthase (TSS) cDNA and genomic DNA clones, as well as determination of the steady state level of TSS mRNA in response to elicitor treatment, were investigated. cDNA clones for TSS were isolated from poly (A)+ RNA using a…
71 Citations
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Bioinformatic analysis and northern blotting analysis revealed that the deduced TcSqS protein had high similarity with other plant squalene synthases and a predicted crystal structure similar to other class I isoprenoid biosynthetic enzymes.
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Results suggest either that there exists coordinate expression of separate synthase genes for squalene and botryococcene biosynthesis or that there might be unique physiological conditions controlling the SS vs botryOCoccene synthase activity of a single peptide species.
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Gas chromatography‐mass spectrometry analysis showed that the purified recombinant PpSQS1 protein could produce squalene using FDP as a substrate in the in vitro enzymatic assay, suggesting that Pp SQS 1 is likely involved in the biosynthesis of steroidal saponins in the plant.
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The result of this study could serve as an important step toward the manipulation of triterpenoids biosynthesis in I. obliquus at the level of squalene through engineering better SQS for reintroduction into the mushroom.
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The findings showed that the amaranth SQS is a late-expressed gene that is rapidly expressed at the mid-late stage of seed development, and it was observed that the SQS mRNA levels in stems and roots increased rapidly during the fourto six-leaf stage of development.
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