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  • Articles: DFG German National Licenses  (3)
  • 1985-1989  (3)
  • 1945-1949
  • 1989  (3)
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  • Articles: DFG German National Licenses  (3)
Material
Years
  • 1985-1989  (3)
  • 1945-1949
Year
  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Plant, cell & environment 12 (1989), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Abstract Evidence is drawn from previous studies to argue that C3—C4 intermediate plants are evolutionary intermediates, evolving from fully-expressed C3 plants towards fully-expressed C4 plants. On the basis of this conclusion, C3—C4 intermediates are examined to elucidate possible patterns that have been followed during the evolution of C4 photosynthesis. An hypothesis is proposed that the initial step in C4-evolution was the development of bundle-sheath metabolism that reduced apparent photorespiration by an efficient recycling of CO2 using RuBP carboxylase. The CO2-recycling mechanism appears to involve the differential compartmentation of glycine decarboxylase between mesophyll and bundle-sheath cells, such that most of the activity is in the bundlesheath cells. Subsequently, elevated phosphoenolpyruvate (PEP) carboxylase activities are proposed to have evolved as a means of enhancing the recycling of photorespired CO2. As the activity of PEP carboxylase increased to higher values, other enzymes in the C4-pathway are proposed to have increased in activity to facilitate the processing of the products of C4-assimilation and provide PEP substrate to PEP carboxylase with greater efficiency. Initially, such a ‘C4-cycle’ would not have been differentially compartmentalized between mesophyll and bundlesheath cells as is typical of fully-expressed C4 plants. Such metabolism would have limited benefit in terms of concentrating CO2 at RuBP carboxylase and, therefore, also be of little benefit for improving water- and nitrogen-use efficiencies. However, the development of such a limited C4-cycle would have represented a preadaptation capable of evolving into the leaf biochemistry typical of fully-expressed C4 plants. Thus, during the initial stages of C4-evolution it is proposed that improvements in photorespiratory CO2-loss and their influence on increasing the rate of net CO2 assimilation per unit leaf area represented the evolutionary ‘driving-force’. Improved resourceuse efficiency resulting from an efficient CO2-concentrating mechanism is proposed as the driving force during the later stages.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Plant, cell & environment 12 (1989), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Abstract Photosynthetic metabolism was investigated in leaves of five species of Flaveria (Asteraceac), all previously considered to be C4 plants. Leaves were exposed to 14CO2 for different intervals up to 16s. Extrapolation of 14C-product curves to zero time indicated that only F. trinervia and F.bidentis assimilated atmospheric CO2 exclusively through phosphoenolpyruvate carboxylase. The proportion of direct fixation of 14CO2 by ribulose-I, 5-bisphosphate carboxylase/oxygenase (Rubisco) ranged from 5 to 10% in leaves of F. australasica. F. palmeri and F. vaginata.Protoplasts of leaf mesophyll and bundle sheath cells were utilized to examine the intercellular compartmentation of principal photosynthetic enzymes. Leaves of F. australasica, F. palmeri and F. vaginata contained 5 to 7% of the leaf's Rubisco activity in the mesophyll cells, while leaves of F. trinervia and F. bidentis contained at most 0.2 to 0.8% of such activity in their mesophyll cells. Thus, F. trinervia and F. bidentis have the complete C4 syndrome, while F. australasica, F. palmeri and F. vaginata are less advanced, C4-like species.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Histochemistry and cell biology 90 (1989), S. 379-381 
    ISSN: 1432-119X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Mushrooms were cut into vertical and horizontal sections. These sections were blotted onto nitrocellulose sheets and the sheets were then stained for tyrosinase using l-dopa. Tyrosinase was localized throughout the mushroom tissues but more enzyme was located in the epidermis of the cap, the gill region, and the stipe. Preincubation of the nitrocellulose sheets in specific inhibitors of tyrosinase completely blocked enzyme staining, suggesting that the enzyme stained areas on the nitrocellulose blots were regions of tyrosinase activity. Immunochemical localization of tyrosinase was similar to that observed by histochemical staining. Nitrocellulose blotting of mushrooms allows localizations of enzyme at the whole tissue level and may be useful for other enzymes in mushrooms as well.
    Type of Medium: Electronic Resource
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