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Localization of chloroplast ribosomal protein genes onSpirodela oligorhizachloroplast DNA

โœ Scribed by Mark Posno; Anja Vliet; Gert S. P. Groot


Book ID
104756718
Publisher
Springer-Verlag
Year
1986
Tongue
English
Weight
721 KB
Volume
10
Category
Article
ISSN
0172-8083

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โœฆ Synopsis


Three chloroplast ribosomal protein genes have been located on Spirodela chloroplast DNA. (1) rpsl4 was physically mapped at the central region of the large single copy region by heterologous hybridization with the corresponding gene of Marchantia chloroplast DNA. (2) Chloroplast ribosomal protein C-$23 was detected by immunoprecipitation with a polyspecific antiserum against 30S chloroplast ribosomal proteins among the in vitro translation products of mRNAs selected by Spirodela PstI-D chloroplast DNA fragment. (3) We have previously reported that Spirodela BamHI-G chloroplast DNA fragment encodes a 14-15 kD 50S chloroplast ribosomal protein (Posno et al. 1985 Curt Genet 9 : 211-219). Here we show that the homologous Spinacia chloroplast DNA fragment SalI-9 additionally directs the synthesis of another 50S chloroplast ribosomal protein in a DNA dependent E. coli cellfree system. This was confirmed by molecular weight determination, immunoprecipitation and competition immunoprecipitation experiments, mRNA selection experiments revealed that this additional chloroplast ribosomal protein gene is present on Spirodela chloroplast DNA as well, but is not expressed in the E. coli cellfree system. The identity of this 50S chloroplast ribosomal protein could not be established unambiguously, since two-dimensional gel analysis revealed that this protein comigrated, depending on the experiment, with C-L11 (26 kD) or with C-L24 (17 kD).


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Localization of three chloroplast riboso
โœ Mark Posno; Dick J. Torenvliet; Henk Lustig; Marjolein Noort; Gert S. P. Groot ๐Ÿ“‚ Article ๐Ÿ“… 1985 ๐Ÿ› Springer-Verlag ๐ŸŒ English โš– 822 KB

In order to determine the localization of ribosomal protein genes on the chloroplast genome of Spirodela, we have followed two different approaches: First, antisera were prepared against purified 30S, 50S and 70S chloroplast ribosomal proteins from Spinacia. These antisera react with about two third