1962
DOI: 10.1016/0006-3002(62)90061-6
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Incorporation of 14C-labelled amino acids into sporidesmolide I by Pithomyces chartarum (Sporidesmium bakeri)

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Cited by 14 publications
(6 citation statements)
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“…On this hypothesis, the biosynthetic system will accept either L-valine for synthesis of sporidesmolide I containing a D-valine residue, or erythro-L-isoleucine for sporidesmolide I1 containing a threo-D-isoleucine residue. This is consistent with the known ability of Pithomyces chartarum to incorporate erythro-L-isoleucine into sporidesmolide isoleucine residues (Butler et al 1962) and with the ability of L-valine completely to inhibit biosynthesis of sporidesmolides containing such residues (unpublished observations). With erythro-L-isoleucine present in excess, sporidesmolide I1 would similarly be synthesized to the exclusion of sporidesmolide I.…”
Section: Discussionsupporting
confidence: 71%
See 1 more Smart Citation
“…On this hypothesis, the biosynthetic system will accept either L-valine for synthesis of sporidesmolide I containing a D-valine residue, or erythro-L-isoleucine for sporidesmolide I1 containing a threo-D-isoleucine residue. This is consistent with the known ability of Pithomyces chartarum to incorporate erythro-L-isoleucine into sporidesmolide isoleucine residues (Butler et al 1962) and with the ability of L-valine completely to inhibit biosynthesis of sporidesmolides containing such residues (unpublished observations). With erythro-L-isoleucine present in excess, sporidesmolide I1 would similarly be synthesized to the exclusion of sporidesmolide I.…”
Section: Discussionsupporting
confidence: 71%
“…The whole of the sporidesmolide I molecule, except for the N-methyl group, may be derived from L-valine and L-leucine supplied in the medium (Butler et al 1962). Examples of antagonism, both between valine and isoleucine, and between leucine and isoleucine, have been reported (Meister, 1965).…”
Section: Discussionmentioning
confidence: 99%
“…For isolation of depsipeptides, the organisms were grown on potato glucose agar slopes, and spores washed from these with sterile 0.05% (v/v) Lissapol N (Imperial Chemical Industries Ltd., Millbank, London) were used for inoculum. The medium for Pithomyces chartarum was potato + carrot extract (Done, Mortimer, Taylor & Russell, 1961), and that for IMI 101184 and P. maydicus IMI 46232 was the salts +glucose + asparagine medium of Ross (Butler, Russell & Clarke, 1962). For P. maydicus 1~198084 and for IMI 102682 this medium was enriched with yeast extract (0.1 yo, w/v; 'Difco' brand, Baird & Tatlock, Ltd., Chadwell Heath, Essex).…”
mentioning
confidence: 99%
“…Culture media were sterilized by heating at 1 2 1 "C for 25 min in an autoclave. Sporulation medium contained: sodium acetate trihydrate, 2 g ; Bacto-tryptone, 2 g ; KCI, 0.25 g; MgS04.7H,0, 0.25 g; KH2P04, 0.5 g; FeS0,.7H20, 5 mg; Ca(N03),.4H20, 30 mg; trace-metal solution (Butler, Russell & Clarke, 1962), 5 ml; and distilled water to I 1. To determine the effect of carbon source and concentration on sporulation, the sodium acetate was altered in concentration or replaced by another carbon compound.…”
Section: Methodsmentioning
confidence: 99%