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Behaviour of tritium-labelled isopenicillin N and 6-aminopenicillanic acid as potential penicillin precursors in an extract of Penicillum chrysogenum

机译:标记的异青霉素N和6-氨基青霉酸作为产黄青霉提取物中潜在的青霉素前体的行为

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p1. sup3/supH was incorporated into solvent-soluble penicillin from isopenicillin N and 6-aminopenicillanic acid sup3/supH-labelled in the 2β-methyl group when the labelled compounds were incubated with a crude extract of Penicillum chrysogenum. 2. With a soluble protein fraction of the extract incorporation from isopenicillin N occurred on addition of phenyl-acetyl-CoA. 3. Labelled benzylpenicillin was isolated after incubation of the crude extract with phenylacetyl-CoA and isopenicillin and the addition of unlabelled benzylpenicillin as a carrier. 4. No incorporation of sup3/supH into solvent-soluble penicillin was detected on incubation of these extracts with penicillin N./p
机译:> 1。当标记的化合物与粗品一起孵育时,将 3 H从异青霉素N和6-氨基青霉酸 3 H-标记的2β-甲基基团引入可溶于溶剂的青霉素产黄青霉的提取物。 2.在提取物中有可溶性蛋白质部分的情况下,通过加入苯基-乙酰基-CoA,从异青霉素N掺入。 3.在粗提取物与苯乙酰基-CoA和异青霉素一起温育并加入未标记的苄青霉素作为载体后,分离出标记的苄青霉素。 4.在将这些提取物与青霉素N一起温育后,未发现 3 H掺入溶剂可溶性青霉素中。

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