Fractionation of the enzyme system responsible for gramicidin S biosynthesis

1. 1. The enzyme system participating in gramicidin S formation was fractionated by precipitation with (NH 4) 2SO 4 and by column chromatography using hydroxylapatite, DEAE-Sephadex amd Sephadex G-200 to investigate the mechanism of gramicidin S biosynthesis. 2. 2. The enzyme system was resolved int...

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Published inBiochimica et biophysica acta Vol. 208; no. 3; pp. 496 - 508
Main Authors Otani, Shuzo, Yamanoi, Taketo, Saito, Yoshitaka
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.06.1970
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ISSN0304-4165
0006-3002
1872-8006
DOI10.1016/0304-4165(70)90224-2

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Abstract 1. 1. The enzyme system participating in gramicidin S formation was fractionated by precipitation with (NH 4) 2SO 4 and by column chromatography using hydroxylapatite, DEAE-Sephadex amd Sephadex G-200 to investigate the mechanism of gramicidin S biosynthesis. 2. 2. The enzyme system was resolved into four protein fractions, which were designated as Fr-1, Fr-2, Fr-3 and Fr-4 in the order of elution from a hydroxylapatite column. Each separated enzyme fraction failed to form gramicidin S. The formation was achieved when Fr-3 and Fr-4 were combined. It was demonstrated that the addition of Fr-1 to the combined enzyme system was essential in obtaining full enzymatic activity for gramicidin S formation, although the role of Fr-1 in gramicidin S formation was left unclarified. 3. 3. In DEAE-Sephadex column chromatography of Fr-4, a phenylalanine-activating fraction (Fr-4-D-I) was separated from a proline-activating fraction (Fr-4-D-I). With wach separated enzyme fraction, neither gramicidin S nor d-phenylalanyl- L-prolyl diketopiperazine was formed, but D-phenylalanyl- L-prolyl diketopiperazine formation was restored following a combination of these enzyme fractions. When a phenylalanine-activating fraction (Fr-2 + 3-S-II) originating from Fr-2 and Fr-3 was added to Fr-4-D-II, the activity of gramicidin S formation appeared in addition to D-phenylalanyl- L-prolyl diketopiperazine formation. 4. 4. The activating enzymes of the constituent amino acids of gramicidin S except for phenylalanine were not separated by any methods adopted in the experiments.
AbstractList 1. 1. The enzyme system participating in gramicidin S formation was fractionated by precipitation with (NH 4) 2SO 4 and by column chromatography using hydroxylapatite, DEAE-Sephadex amd Sephadex G-200 to investigate the mechanism of gramicidin S biosynthesis. 2. 2. The enzyme system was resolved into four protein fractions, which were designated as Fr-1, Fr-2, Fr-3 and Fr-4 in the order of elution from a hydroxylapatite column. Each separated enzyme fraction failed to form gramicidin S. The formation was achieved when Fr-3 and Fr-4 were combined. It was demonstrated that the addition of Fr-1 to the combined enzyme system was essential in obtaining full enzymatic activity for gramicidin S formation, although the role of Fr-1 in gramicidin S formation was left unclarified. 3. 3. In DEAE-Sephadex column chromatography of Fr-4, a phenylalanine-activating fraction (Fr-4-D-I) was separated from a proline-activating fraction (Fr-4-D-I). With wach separated enzyme fraction, neither gramicidin S nor d-phenylalanyl- L-prolyl diketopiperazine was formed, but D-phenylalanyl- L-prolyl diketopiperazine formation was restored following a combination of these enzyme fractions. When a phenylalanine-activating fraction (Fr-2 + 3-S-II) originating from Fr-2 and Fr-3 was added to Fr-4-D-II, the activity of gramicidin S formation appeared in addition to D-phenylalanyl- L-prolyl diketopiperazine formation. 4. 4. The activating enzymes of the constituent amino acids of gramicidin S except for phenylalanine were not separated by any methods adopted in the experiments.
Author Saito, Yoshitaka
Yamanoi, Taketo
Otani, Shuzo
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crossref_primary_10_1038_newbio239043a0
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Cites_doi 10.1093/oxfordjournals.jbchem.a128748
10.1021/bi00876a015
10.1016/0006-291X(66)90495-5
10.1016/0304-4165(66)90436-3
10.1021/bi00843a036
10.1021/bi00860a037
10.1016/0006-291X(65)90505-X
10.1111/j.1432-1033.1968.tb00388.x
10.1042/bj1020586
10.1016/S0021-9258(17)30999-7
10.1016/0003-9861(56)90183-7
10.1016/0006-291X(64)90399-7
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Snippet 1. 1. The enzyme system participating in gramicidin S formation was fractionated by precipitation with (NH 4) 2SO 4 and by column chromatography using...
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SubjectTerms Adenosine Triphosphate - metabolism
Bacillus - enzymology
Carbon Isotopes
Chemical Precipitation
Chromatography, Gel
Chromatography, Ion Exchange
Enzymes - isolation & purification
Hydroxyapatites
Isomerases
Methods
Phenylalanine
Phosphorus Isotopes
Piperazines
Proline
Quaternary Ammonium Compounds
Sulfates
Tyrothricin - biosynthesis
Title Fractionation of the enzyme system responsible for gramicidin S biosynthesis
URI https://dx.doi.org/10.1016/0304-4165(70)90224-2
https://www.ncbi.nlm.nih.gov/pubmed/5506580
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