The pattern of protein and nucleic acid synthesis in germinating spores of Phycomyces blakesleeanus
โ Scribed by Assche, J. A. ;Carlier, A. R.
- Publisher
- Springer-Verlag
- Year
- 1973
- Weight
- 456 KB
- Volume
- 93
- Category
- Article
- ISSN
- 0003-9276
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โฆ Synopsis
Synthesis of proteins, RNA and DNA is measured by incorporation of labelled precursors at different times during germination of Phycomyces spores.
RNA and protein synthesis increases immediately after activation. DNA synthesis begins at a later stage (:[: 8 h) of germination when germ tubes are already present. Nuclear division occurs earlier in germination (โข 4--5 h) and is accompanied by a decrease in RNA synthesis. It can be concluded that at least most of the dormant spores are in the G2 phase of the cell cycle.
Analysis of ribosomal RNA after pulse-chase labelling shows only three labelled compounds: a precursor molecule (2.25 โข 10 e daltons) and the two mature ribosomal RNA compounds (1.4 โข 106 and 0.7 โข 106 daltons). This suggests that the two rRNAs are formed directly from the precursor molecu]e. Cycloheximide totally blocks the transformation of the ribosomal precursor molecu]e into mature rRNA.
๐ SIMILAR VOLUMES
Protein and nucleic acid synthesis is usually determined by measuring the incorporation of labeled precursors of low molecular weight. This is done either by autoradiographic methods or by measuring incorporation of the acid-soluble precursors into acid-insoluble products. Spurious incorporation of
Bacillus subtilis strain PB 2427 temperature sensitive in the synthesis of RNA during spore germination and outgrowth has been characterized to some extent. At non permissive temperature (46 degrees C) strain PB 2427 synthesizes stable and unstable RNA for 50 min from the beginning of germination an
## Abstract | I. | Introduction | 306 | | II. | Supramolecular Structure Characterization | 308 | | | A.โA Protein Is Used as a โHookโ | 309 | | | โโโ1.โImmunoโPrecipitation | 309 | | | โโโ2.โTagging with a PolyโHistidine Sequence | 310 | | | โโโ3.โDirect Analysis of Large Protein Complexes | 3