Deletion map of the Escherichia coli K-12 dnaB gene |
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Authors: | Anna H Nagy Géza Erdös Natalia N Beliaeva and István Gyurján |
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Institution: | (1) Department of Genetics, Eötvös Loránd University, Muzeum krt 4/a, H-1088 Budapest, Hungary;(2) Department of Physiology and Biochemistry of Plants, Leningrad State University, 164 Leningrad, USSR |
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Abstract: | Summary Acid phosphatase isoenzymes of Chlamydomonas reinhardii were investigated by isoelectric focusing in polyacrylamide gel systems. In this paper we describe in detail an original method for isoelectric focusing of acid phosphatases extracted from wildtype and acid phosphatase-lacking mutant algae, obtained from Laboratoire de Génetique of University of Liège. Three isoenzymes can be separated from the buffer-soluble components of these cells. An additional isoenzyme type can be visualized using the nonionic detergent NP40 as solubilizer. We conclude that these four isoenzymes are releated to the structural gene of the soluble constitutive acid phosphatase, which was shown by their appearance in P
2 and their total absence in mutant P
a. The pl values of soluble constitutive acid phosphatase isoenzymes range between pH 5.2 and 6.2. As a result of treatment with NP40 the extracts from both wild-type and mutant lines contain two additional active phosphatase forms which can be characterized by their high heat resistance and low pI values. These enzymes are fully active using either -naphthyl phosphate or different acetate esters as substrates. |
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