Zur physiologie der aminbildung bei der marinen rotalge Polysiphonia urceolata |
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Authors: | T Hartmann B Aufermann |
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Institution: | 1. Pharmakognostisches Institut der Universit?t Bonn, Bonn, Germany
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Abstract: | The ceramiaceaen Polysiphonia urceolata rapidly degrades 14C(U)-L-leucine, added to sea water at a final concentration of 2.5x10-5 M/l, to isoamylamine. Under experimental conditions, 22% of the total radioactivity is found in the amine within 160 min. The amino acid decarboxylase responsible for this reaction has been characterized by Hartmann (1972a). No other mechanisms of leucine degradation could be detected, and the rate of 14C-incorporation into algal proteins is considerably lower than that of decarboxylation. The rate of decarboxylation is optimal at a leucine concentration of about 5x10-5 M/l. The amine formed is found in almost equal amounts in algal extract and environment. No further degradation of isoamylamine could be detected. The amine is a metabolic end product in P. urceolata. When 14C-isoamylamine is used as a tracer, relatively high amounts of amine are found in the algal extracts. It is supposed that the amine does not accumulate within the algal cells, but rather is bound to the acid polysaccharides of the cell walls by means of ionic exchange. The results strongly suggest that decarboxylation is the main route by which P. ureolata metabolizes amino acids from the environment which are substrates of the decarboxylase. The endogenous amino acid pool does not seem to be available to the enzyme as a substrate source. A possible ecological significance of amino acid decarboxylations is discussed. |
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