Transcription activity of a DNA-protein complex isolated from spinach plastids

Eur J Biochem. 1979 Jul;98(1):285-92. doi: 10.1111/j.1432-1033.1979.tb13187.x.


A DNA . protein complex of about 150 S is isolated from purified spinach chloroplasts by Sepharose 4B gel filtration. A DNA-dependent RNA polymerase activity is found associated with the complex. This DNA protein complex is able to initiate RNA chains in vitro. The RNA synthesis is more dependent on CTP than other nucleoside triphosphates. 50% of the activity is still present with 0.6 M KCl. The temperature optimum occurs between 30 degrees C and 35 degrees C. Rifampicin and rifamycin SV have no inhibitory effect. TNA products have been characterized by gel filtration and by hybridization with chloroplast DNA (ctDNA). At the beginning of transcription DNA products are linked to the transcription complex and are later detached. The molecular weight of the product ranges between 0.07 X 10(6) and 2 X 10(6). A part of the product (3--4%) has a molecular weight higher than 2 X 10(6). No endogenous RNase activity was present during the molecular weight determinations experiments. Hybridization experiments show that at least 75% of the RNA products are hybridizable with ctDNA and that 40% of these products are composed of chloroplast ribosomal RNA, showing that rDNA is preferentially transcribed.

MeSH terms

  • Chloroplasts / metabolism*
  • DNA-Directed RNA Polymerases / metabolism*
  • Deoxyribonucleoproteins / metabolism*
  • Kinetics
  • Molecular Weight
  • Nucleic Acid Hybridization
  • Nucleoproteins / metabolism*
  • Plants
  • RNA / biosynthesis
  • Ribonucleases / metabolism
  • Transcription, Genetic*


  • Deoxyribonucleoproteins
  • Nucleoproteins
  • RNA
  • DNA-Directed RNA Polymerases
  • Ribonucleases