Synthesis of (di)adenosine polyphosphates by non-ribosomal peptide synthetases (NRPS) |
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Authors: | Dieckmann R Pavela-Vrancic M von Döhren H |
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Affiliation: | Max-Volmer-Institut für Biophysikalische Chemie und Biochemie, Technische Universit?t Berlin, Franklinstrasse 20, 10587 Berlin, Germany. |
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Abstract: | In response to nutritional stress conditions, Bacillus brevis produces the cyclodecapeptide antibiotic tyrocidine via tyrocidine synthetase, a multifunctional non-ribosomal peptide synthetase. The apo-form of tyrocidine synthetase 1 forms adenosine (5')tetraphospho(5')adenosine, when incubated with MgATP(2-), amino acid and inorganic pyrophosphatase. The synthesis is an intrinsic property of the adenylation domain, is strictly dependent upon the amino acid, and proceeds from a reverse reaction of adenylate formation involving a second ATP molecule. In the presence of tri- or tetrapolyphosphate preferential synthesis of adenosine 5'-tetraphosphate and adenosine 5'-pentaphosphate occurs, respectively. A potential involvement of adenosine (5')-n-phospho(5')adenosine in the regulation of the biosynthetic process has been suggested. |
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