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Quantification and intracellular distribution of ribulose-1,5-bisphosphate carboxylase in Thiobacillus neapolitanus,as related to possible functions of carboxysomes
Authors:R F Beudeker  G A Codd  J G Kuenen
Institution:(1) Department of Microbiology, University of Groningen, Kerklaan 30, 9751 NN Haren, The Netherlands;(2) Department of Biological Sciences, University of Dundee, DD1 4HN Dundee, UK;(3) Department of Microbiology, Delft University of Technology, Julianalaan 67A, 2628 BC Delft, The Netherlands
Abstract:Ribulose-1,5-bisphosphate carboxylase (RuBPCase) has been quantified by immunological methods in Thiobacillus neapolitanus cultivated under various growth conditions in the chemostat at a fixed dilution rate of 0.07 h-1. RuBPCase was a major protein in T. neapolitanus accounting for a maximum of 17% of the total protein during CO2 limitation and for a minimum of 4% during either ammonium- or thiosulfate limitation in the presence of 5% CO2 (v/v) in the gasphase. The soluble RuBPCase (i.e. in the cytosol) and the particulate RuBPCase (i.e. in the carboxysomes) were shown to be immunologically identical. The intracellular distribution of RuBPCase protein between carboxysomes and cytosol was quantified by rocket immunoelectrophoresis. The particulate RuBPCase content, which correlated with the volume density of carboxysomes, was minimal during ammonium limitation (1.3% of the total protein) and maximal during CO2 limitation (6.8% of the total protein). A protein storage function of carboxysomes is doubtful since nitrogen starvation did not result in degradation of particulate RuBPCase within 24 h. Proteolysis of RuBPCase was not detected. Carboxysomes, on the other hand, were degraded rapidly (50% within 1 h) after change-over from CO2 limitation to thiosulfate limitation with excess CO2. Particulate RuBPCase protein became soluble during this degradation of carboxysomes, but this did not result in an increase in soluble RuBPCase activity. Modification of RuBPCase resulting in a lower true specific activity was suggested to explain this phenomenon. The true specific activity was very similar for soluble and particulate RuBPCase during various steady state growth conditions (about 700 nmol/min·mg RuBPCase protein), with the exception of CO2-limited growth when the true specific activity of the soluble RuBPCase was extremely low (260 nmol/min ·mg protein). When chemostat cultures of T. neapolitanus were exposed to different oxygen tensions, neither the intracellular distribution of RuBPCase nor the content of RuBPCase were affected. Short-term labelling experiments showed that during CO2 limitation, when carboxysomes were most abundant, CO2 is fixed via the Calvin cycle. The data are assessed in terms of possible functions of carboxysomes.Abbreviations RuBPCase ribulose-1,5-bisphosphate carboxylase - PEP phosphoenolpyruvate - RIE rocket immunoelectrophoresis - CIE crossed immunoelectrophoresis
Keywords:Ribulose-1  5-bisphosphate carboxylase  Carboxysomes  Thiobacillus neapolitanus  Chemolithotroph  Autotroph
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