Analysis of the <i>Euglena gracilis</i> chloroplast genome: Fragment <i>Eco-I</i> encodes the gene for the <i>M</i><sub>r</sub> 32 000–33 000 thylakoid protein of photosystem II reaction center
Author(s)
Keller, Mario
Date issued
1982
In
FEBS Letters
Vol
189
No
1
From page
133
To page
137
Subjects
<i>Euglena gracilis</i> Chloroplast genome Thylakoid membrane Protein 32 00 <i>M</i><sub>r</sub> Restriction enzyme DNA fragment <i>Eco-I</i>
Abstract
The DNA fragment <i>Eco</i>-I (4700 kilobasepairs) from the circular chloroplast genome of <i>Euglena gracilis</i> is shown to be transcribed in etioplasts at all stages of light-induced plastid development and in fully differentiated chloroplasts. Major stable transcription products are mRNAs of 14S and 17S. Using a rabbit reticulocyte lysate translation system we can show that the fragment <i>Eco</i>-I selects a mRNA which directs the synthesis of a <i>M</i><sub>r</sub> 32 000–33 000 polypeptide. <i>Eco</i>-I also hybridizes with a 330 basepair DNA probe cut from within the spinach chloroplast gene encoding the <i>M</i><sub>r</sub> 32 000 thylakoid membrane protein of the photosystem II reaction center. We conclude that the fragment <i>Eco</i>-I carries the corresponding <i>Euglena gracilis</i> chloroplast gene.
Publication type
journal article
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Stutz_Erhard_-_Analysis_of_the_Euglena_gracilis_20090603.pdf
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