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Abnormally high concentrations of beryllium, scandium, chromium, and iodine have been found in algae; of copper and arsenic in both the soft and skeletal parts of invertebrate animals; and of zirconium and cerium in plankton.
DWF1 or DHCR24 orthologs have not been found in algae except in N. oceanica and the diatom Fragilariopsis cylindrus.
Nonetheless, Tic and Toc components have previously been found in algae containing more than two membranes [ 82, 83].
It is ubiquitous in lower and higher plants and has also been found in algae [ 2], fungi [ 3], and even mammalian brain tissue [ 4].
Cellulose crystal structure has been determined (Nishiyama et al. 2002, 2003) and I alpha and I beta crystal forms have been found in algae and plants (Atalla and VanderHart 1984).
Although homologues for the fission yeast wee1 have been identified in several plant species [ 4- 6], a full length homologue of CDC25 has only been found in algae [ 7] while higher plant genomes have a partial CDC25 gene that lacks the regulatory domain [ 8, 9].
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Among these, ion channels that open when a chemical co-factor, all-trans-retinal, absorbs photons were found in algae.
Lhcb6 also appeared during the evolution of land plants and no ortholog is found in algae, either in EST or genomic databases [32].
However, no trihelix genes were found in algae.
P2X receptors are found in algae [ 42] as well as in Dictyostelium discoideum [ 43].
Aureochromes are photoreceptors that detect blue light and are found in algae.
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