Capacity of Enzymes of the Euphorbiacea Aleurites montana Involved in C 0 2- Fixation, Compared to Plants Having C3-, C4- and Crassulacean Acid Metabolism

نویسندگان

  • Norbert Grotjohann
  • Georg H. Schmid
چکیده

Norbert Grotjohann3, Ping H eb and Georg H. Schmid3-* a Lehrstuhl für Zellphysiologie, Fakultät für Biologie, Universität Bielefeld, Postfach 10 01 31, 33501 Bielefeld, Bundesrepublik Deutschland. Fax: +49 (521) 1066410. E-mail: [email protected] b Central South Forestry University, Zhuzhou/Hunan 41206, People’s Republic of China * Author for correspondence and reprint requests Z. Naturforrsch. 55c, 383-391 (2000); received March 2/April 7, 2000 Dedicated to Professor Wilhelm Menke on the occasion o f his 90th birthday Aleurites montana, Phosphoenolpyruvate Carboxylase, Malic Enzyme, Malate Dehydrogenase, Ribulose Bisphosphate Carboxylase Capacities of phosphoenolpyruvate carboxylase (PEP-Co), ribulose bisphosphate carbox­ ylase (Rubisco), NADP+ malic enzyme (ME) and of malate dehydrogenase (MDH) were measured in the Euphorbiacea Aleurites montana, grown under 700 ppm C 0 2 for four weeks prior to enzyme extraction. For comparison Bryophyllum daigremontiana (CAM), Saccharum officinarum (C4) and Capsicum frutescens (C3) were treated in the same way. PEP-Co capac­ ity of Aleurites was in the range of 12-, that of Capsicum approx. 26 nmol x min-1 x mg protein-1, without significant influence of the light period or C 0 2-treatment. In contrast, the activity of the enzyme from Saccharum was. depending on the duration of light, 160respec­ tively 96 times higher than that of the tung-oil tree. In Bryophyllum a rather low activity in the morning was increased during the day to approx. 230 nmol x min-1 x mg protein-1 in plants grown in the greenhouse and to approx. 115 nmol x min-1 x mg protein-1 in those from the growth chamber. Malate was hardly detectable in extracts of Aleurites, whereas it was high in Bryophyllum , depending on the light period. The ratio of average PEP-Co to Rub-Co capacity was high for the CAM-plant (20:1), somewhat lower for sugar cane (10:1), but almost at equality for Aleurites (0.9:1) and chilli (0.8:1). For the NADP+ malic enzyme, low capacity (20 to 28 nmol x min-1 x mg protein-1) was found for Aleurites and for Capsi­ cum!, whereas it was 10 to 17 times higher in Saccharum. In Bryophyllum , the activity was up to 80 nmol x min-1 x mg p r o te in , dependent on light period. MDH capacity was ex­ tremely high in all plants investigated. Highest rates (10-20 |j,mol x min-1 x mg protein-1), were obtained for Bryophyllum , followed by sugar cane and Capsicum with 5 -8 [.imol x min-1 x mg protein-1. Again, the lowest capacity was found in extracts of Aleurites with approx. 1.3 to 1.6 ^unol x min-1 x m protein-1. Thus, in Aleurites montana no indication for C4or Crassulacean acid metabolism was obtained. Therefore, the earlier observed very efficient uptake of C 0 2 cannot be explained by a high expression of the PEP-Co protein, known to occur in CAMand C4-plants.

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Capacity of enzymes of the euphorbiacea Aleurites montana involved in CO2-fixation, compared to plants having C3-, C4- and Crassulacean acid metabolism.

Capacities of phosphoenolpyruvate carboxylase (PEP-Co), ribulose bisphosphate carboxylase (Rubisco), NADP+ malic enzyme (ME) and of malate dehydrogenase (MDH) were measured in the Euphorbiacea Aleurites montana, grown under 700 ppm CO2 for four weeks prior to enzyme extraction. For comparison Bryophyllum daigremontiana (CAM). Saccharum officinarum (C4) and Capsicum frutescens (C3) were treated ...

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تاریخ انتشار 2013