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 in | Biochimica et biophysica acta Vol. 208; no. 3; pp. 496 - 508 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
01.06.1970
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Subjects | |
Online Access | Get full text |
ISSN | 0304-4165 0006-3002 1872-8006 |
DOI | 10.1016/0304-4165(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. |
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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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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/5506580$$D View this record in MEDLINE/PubMed |
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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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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 |
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