Localization of newly synthesized indoIe-3-methylglucosinolate (= glucobrassicin) in vacuoles from horseradish (Armoracia rusticana)
The presence and concentration of indole-3-methylglucosinolate [= glucobrassicin; 0.49 μmol (g dry weight)-1] and its 1-methoxy derivative [0.38 umol (g dry weight)−1] in Armoracia rusticana P. Gärtner, B. Meyer and Scherb, storage roots were measured. The storage tissue contains L-tryptophan [1.63...
Ausführliche Beschreibung
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| Autor*in: |
Helmlinger, Jürgen [verfasserIn] Rausch, Thomas [verfasserIn] Hilgenberg, Willy [verfasserIn] |
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| Format: |
E-Artikel |
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| Erschienen: |
Oxford, UK: Blackwell Publishing Ltd ; 1983 |
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| Schlagwörter: |
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| Umfang: |
Online-Ressource |
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| Reproduktion: |
2006 ; Blackwell Publishing Journal Backfiles 1879-2005 |
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| Übergeordnetes Werk: |
In: Physiologia plantarum - Oxford [u.a.] : Wiley-Blackwell, 1948, 58(1983), 3, Seite 0 |
| Übergeordnetes Werk: |
volume:58 ; year:1983 ; number:3 ; pages:0 |
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| DOI / URN: |
10.1111/j.1399-3054.1983.tb04185.x |
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| 520 | |a The presence and concentration of indole-3-methylglucosinolate [= glucobrassicin; 0.49 μmol (g dry weight)-1] and its 1-methoxy derivative [0.38 umol (g dry weight)−1] in Armoracia rusticana P. Gärtner, B. Meyer and Scherb, storage roots were measured. The storage tissue contains L-tryptophan [1.63 μmol (g dry weight)-1], which is the common precursor amino acid of the indoleglucosinolates. Tissue cylinders convert [14C]-l-tryptophan efficiently to the indoleglucosinolates (25%) in vivo. The conversion of [14C]-l-tryptophan to indole-3-methylgluco-sinolate shows biphasic kinetics.A fraction rich in vacuoles was prepared from tissue sections to which [14C]-l-tryp-tophan had been fed and allowed to be metabolized. The predominantly vacuolar location of both L-tryptophan and the indoleglucosinolates is demonstrated by correlation with the vacuolar marker acid phosphatase.The significance for the regulation of the indoleglucosinolate biosynthesis and the role of indole-3-methylglucosinolate as a potential auxin precursor are discussed. | ||
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10.1111/j.1399-3054.1983.tb04185.x doi (DE-627)NLEJ240978722 DE-627 ger DE-627 rakwb Helmlinger, Jürgen verfasserin aut Localization of newly synthesized indoIe-3-methylglucosinolate (= glucobrassicin) in vacuoles from horseradish (Armoracia rusticana) Oxford, UK Blackwell Publishing Ltd 1983 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The presence and concentration of indole-3-methylglucosinolate [= glucobrassicin; 0.49 μmol (g dry weight)-1] and its 1-methoxy derivative [0.38 umol (g dry weight)−1] in Armoracia rusticana P. Gärtner, B. Meyer and Scherb, storage roots were measured. The storage tissue contains L-tryptophan [1.63 μmol (g dry weight)-1], which is the common precursor amino acid of the indoleglucosinolates. Tissue cylinders convert [14C]-l-tryptophan efficiently to the indoleglucosinolates (25%) in vivo. The conversion of [14C]-l-tryptophan to indole-3-methylgluco-sinolate shows biphasic kinetics.A fraction rich in vacuoles was prepared from tissue sections to which [14C]-l-tryp-tophan had been fed and allowed to be metabolized. The predominantly vacuolar location of both L-tryptophan and the indoleglucosinolates is demonstrated by correlation with the vacuolar marker acid phosphatase.The significance for the regulation of the indoleglucosinolate biosynthesis and the role of indole-3-methylglucosinolate as a potential auxin precursor are discussed. 2006 Blackwell Publishing Journal Backfiles 1879-2005 |2006|||||||||| Indole-3-acetic acid biosynthesis Rausch, Thomas verfasserin aut Hilgenberg, Willy verfasserin aut In Physiologia plantarum Oxford [u.a.] : Wiley-Blackwell, 1948 58(1983), 3, Seite 0 Online-Ressource (DE-627)NLEJ243927738 (DE-600)2020837-6 1399-3054 nnns volume:58 year:1983 number:3 pages:0 http://dx.doi.org/10.1111/j.1399-3054.1983.tb04185.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 58 1983 3 0 |
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10.1111/j.1399-3054.1983.tb04185.x doi (DE-627)NLEJ240978722 DE-627 ger DE-627 rakwb Helmlinger, Jürgen verfasserin aut Localization of newly synthesized indoIe-3-methylglucosinolate (= glucobrassicin) in vacuoles from horseradish (Armoracia rusticana) Oxford, UK Blackwell Publishing Ltd 1983 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The presence and concentration of indole-3-methylglucosinolate [= glucobrassicin; 0.49 μmol (g dry weight)-1] and its 1-methoxy derivative [0.38 umol (g dry weight)−1] in Armoracia rusticana P. Gärtner, B. Meyer and Scherb, storage roots were measured. The storage tissue contains L-tryptophan [1.63 μmol (g dry weight)-1], which is the common precursor amino acid of the indoleglucosinolates. Tissue cylinders convert [14C]-l-tryptophan efficiently to the indoleglucosinolates (25%) in vivo. The conversion of [14C]-l-tryptophan to indole-3-methylgluco-sinolate shows biphasic kinetics.A fraction rich in vacuoles was prepared from tissue sections to which [14C]-l-tryp-tophan had been fed and allowed to be metabolized. The predominantly vacuolar location of both L-tryptophan and the indoleglucosinolates is demonstrated by correlation with the vacuolar marker acid phosphatase.The significance for the regulation of the indoleglucosinolate biosynthesis and the role of indole-3-methylglucosinolate as a potential auxin precursor are discussed. 2006 Blackwell Publishing Journal Backfiles 1879-2005 |2006|||||||||| Indole-3-acetic acid biosynthesis Rausch, Thomas verfasserin aut Hilgenberg, Willy verfasserin aut In Physiologia plantarum Oxford [u.a.] : Wiley-Blackwell, 1948 58(1983), 3, Seite 0 Online-Ressource (DE-627)NLEJ243927738 (DE-600)2020837-6 1399-3054 nnns volume:58 year:1983 number:3 pages:0 http://dx.doi.org/10.1111/j.1399-3054.1983.tb04185.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 58 1983 3 0 |
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10.1111/j.1399-3054.1983.tb04185.x doi (DE-627)NLEJ240978722 DE-627 ger DE-627 rakwb Helmlinger, Jürgen verfasserin aut Localization of newly synthesized indoIe-3-methylglucosinolate (= glucobrassicin) in vacuoles from horseradish (Armoracia rusticana) Oxford, UK Blackwell Publishing Ltd 1983 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The presence and concentration of indole-3-methylglucosinolate [= glucobrassicin; 0.49 μmol (g dry weight)-1] and its 1-methoxy derivative [0.38 umol (g dry weight)−1] in Armoracia rusticana P. Gärtner, B. Meyer and Scherb, storage roots were measured. The storage tissue contains L-tryptophan [1.63 μmol (g dry weight)-1], which is the common precursor amino acid of the indoleglucosinolates. Tissue cylinders convert [14C]-l-tryptophan efficiently to the indoleglucosinolates (25%) in vivo. The conversion of [14C]-l-tryptophan to indole-3-methylgluco-sinolate shows biphasic kinetics.A fraction rich in vacuoles was prepared from tissue sections to which [14C]-l-tryp-tophan had been fed and allowed to be metabolized. The predominantly vacuolar location of both L-tryptophan and the indoleglucosinolates is demonstrated by correlation with the vacuolar marker acid phosphatase.The significance for the regulation of the indoleglucosinolate biosynthesis and the role of indole-3-methylglucosinolate as a potential auxin precursor are discussed. 2006 Blackwell Publishing Journal Backfiles 1879-2005 |2006|||||||||| Indole-3-acetic acid biosynthesis Rausch, Thomas verfasserin aut Hilgenberg, Willy verfasserin aut In Physiologia plantarum Oxford [u.a.] : Wiley-Blackwell, 1948 58(1983), 3, Seite 0 Online-Ressource (DE-627)NLEJ243927738 (DE-600)2020837-6 1399-3054 nnns volume:58 year:1983 number:3 pages:0 http://dx.doi.org/10.1111/j.1399-3054.1983.tb04185.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 58 1983 3 0 |
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10.1111/j.1399-3054.1983.tb04185.x doi (DE-627)NLEJ240978722 DE-627 ger DE-627 rakwb Helmlinger, Jürgen verfasserin aut Localization of newly synthesized indoIe-3-methylglucosinolate (= glucobrassicin) in vacuoles from horseradish (Armoracia rusticana) Oxford, UK Blackwell Publishing Ltd 1983 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The presence and concentration of indole-3-methylglucosinolate [= glucobrassicin; 0.49 μmol (g dry weight)-1] and its 1-methoxy derivative [0.38 umol (g dry weight)−1] in Armoracia rusticana P. Gärtner, B. Meyer and Scherb, storage roots were measured. The storage tissue contains L-tryptophan [1.63 μmol (g dry weight)-1], which is the common precursor amino acid of the indoleglucosinolates. Tissue cylinders convert [14C]-l-tryptophan efficiently to the indoleglucosinolates (25%) in vivo. The conversion of [14C]-l-tryptophan to indole-3-methylgluco-sinolate shows biphasic kinetics.A fraction rich in vacuoles was prepared from tissue sections to which [14C]-l-tryp-tophan had been fed and allowed to be metabolized. The predominantly vacuolar location of both L-tryptophan and the indoleglucosinolates is demonstrated by correlation with the vacuolar marker acid phosphatase.The significance for the regulation of the indoleglucosinolate biosynthesis and the role of indole-3-methylglucosinolate as a potential auxin precursor are discussed. 2006 Blackwell Publishing Journal Backfiles 1879-2005 |2006|||||||||| Indole-3-acetic acid biosynthesis Rausch, Thomas verfasserin aut Hilgenberg, Willy verfasserin aut In Physiologia plantarum Oxford [u.a.] : Wiley-Blackwell, 1948 58(1983), 3, Seite 0 Online-Ressource (DE-627)NLEJ243927738 (DE-600)2020837-6 1399-3054 nnns volume:58 year:1983 number:3 pages:0 http://dx.doi.org/10.1111/j.1399-3054.1983.tb04185.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 58 1983 3 0 |
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10.1111/j.1399-3054.1983.tb04185.x doi (DE-627)NLEJ240978722 DE-627 ger DE-627 rakwb Helmlinger, Jürgen verfasserin aut Localization of newly synthesized indoIe-3-methylglucosinolate (= glucobrassicin) in vacuoles from horseradish (Armoracia rusticana) Oxford, UK Blackwell Publishing Ltd 1983 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The presence and concentration of indole-3-methylglucosinolate [= glucobrassicin; 0.49 μmol (g dry weight)-1] and its 1-methoxy derivative [0.38 umol (g dry weight)−1] in Armoracia rusticana P. Gärtner, B. Meyer and Scherb, storage roots were measured. The storage tissue contains L-tryptophan [1.63 μmol (g dry weight)-1], which is the common precursor amino acid of the indoleglucosinolates. Tissue cylinders convert [14C]-l-tryptophan efficiently to the indoleglucosinolates (25%) in vivo. The conversion of [14C]-l-tryptophan to indole-3-methylgluco-sinolate shows biphasic kinetics.A fraction rich in vacuoles was prepared from tissue sections to which [14C]-l-tryp-tophan had been fed and allowed to be metabolized. The predominantly vacuolar location of both L-tryptophan and the indoleglucosinolates is demonstrated by correlation with the vacuolar marker acid phosphatase.The significance for the regulation of the indoleglucosinolate biosynthesis and the role of indole-3-methylglucosinolate as a potential auxin precursor are discussed. 2006 Blackwell Publishing Journal Backfiles 1879-2005 |2006|||||||||| Indole-3-acetic acid biosynthesis Rausch, Thomas verfasserin aut Hilgenberg, Willy verfasserin aut In Physiologia plantarum Oxford [u.a.] : Wiley-Blackwell, 1948 58(1983), 3, Seite 0 Online-Ressource (DE-627)NLEJ243927738 (DE-600)2020837-6 1399-3054 nnns volume:58 year:1983 number:3 pages:0 http://dx.doi.org/10.1111/j.1399-3054.1983.tb04185.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 58 1983 3 0 |
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Localization of newly synthesized indoIe-3-methylglucosinolate (= glucobrassicin) in vacuoles from horseradish (Armoracia rusticana) Indole-3-acetic acid biosynthesis |
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localization of newly synthesized indoie-3-methylglucosinolate (= glucobrassicin) in vacuoles from horseradish (armoracia rusticana) |
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Localization of newly synthesized indoIe-3-methylglucosinolate (= glucobrassicin) in vacuoles from horseradish (Armoracia rusticana) |
| abstract |
The presence and concentration of indole-3-methylglucosinolate [= glucobrassicin; 0.49 μmol (g dry weight)-1] and its 1-methoxy derivative [0.38 umol (g dry weight)−1] in Armoracia rusticana P. Gärtner, B. Meyer and Scherb, storage roots were measured. The storage tissue contains L-tryptophan [1.63 μmol (g dry weight)-1], which is the common precursor amino acid of the indoleglucosinolates. Tissue cylinders convert [14C]-l-tryptophan efficiently to the indoleglucosinolates (25%) in vivo. The conversion of [14C]-l-tryptophan to indole-3-methylgluco-sinolate shows biphasic kinetics.A fraction rich in vacuoles was prepared from tissue sections to which [14C]-l-tryp-tophan had been fed and allowed to be metabolized. The predominantly vacuolar location of both L-tryptophan and the indoleglucosinolates is demonstrated by correlation with the vacuolar marker acid phosphatase.The significance for the regulation of the indoleglucosinolate biosynthesis and the role of indole-3-methylglucosinolate as a potential auxin precursor are discussed. |
| abstractGer |
The presence and concentration of indole-3-methylglucosinolate [= glucobrassicin; 0.49 μmol (g dry weight)-1] and its 1-methoxy derivative [0.38 umol (g dry weight)−1] in Armoracia rusticana P. Gärtner, B. Meyer and Scherb, storage roots were measured. The storage tissue contains L-tryptophan [1.63 μmol (g dry weight)-1], which is the common precursor amino acid of the indoleglucosinolates. Tissue cylinders convert [14C]-l-tryptophan efficiently to the indoleglucosinolates (25%) in vivo. The conversion of [14C]-l-tryptophan to indole-3-methylgluco-sinolate shows biphasic kinetics.A fraction rich in vacuoles was prepared from tissue sections to which [14C]-l-tryp-tophan had been fed and allowed to be metabolized. The predominantly vacuolar location of both L-tryptophan and the indoleglucosinolates is demonstrated by correlation with the vacuolar marker acid phosphatase.The significance for the regulation of the indoleglucosinolate biosynthesis and the role of indole-3-methylglucosinolate as a potential auxin precursor are discussed. |
| abstract_unstemmed |
The presence and concentration of indole-3-methylglucosinolate [= glucobrassicin; 0.49 μmol (g dry weight)-1] and its 1-methoxy derivative [0.38 umol (g dry weight)−1] in Armoracia rusticana P. Gärtner, B. Meyer and Scherb, storage roots were measured. The storage tissue contains L-tryptophan [1.63 μmol (g dry weight)-1], which is the common precursor amino acid of the indoleglucosinolates. Tissue cylinders convert [14C]-l-tryptophan efficiently to the indoleglucosinolates (25%) in vivo. The conversion of [14C]-l-tryptophan to indole-3-methylgluco-sinolate shows biphasic kinetics.A fraction rich in vacuoles was prepared from tissue sections to which [14C]-l-tryp-tophan had been fed and allowed to be metabolized. The predominantly vacuolar location of both L-tryptophan and the indoleglucosinolates is demonstrated by correlation with the vacuolar marker acid phosphatase.The significance for the regulation of the indoleglucosinolate biosynthesis and the role of indole-3-methylglucosinolate as a potential auxin precursor are discussed. |
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| title_short |
Localization of newly synthesized indoIe-3-methylglucosinolate (= glucobrassicin) in vacuoles from horseradish (Armoracia rusticana) |
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http://dx.doi.org/10.1111/j.1399-3054.1983.tb04185.x |
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Rausch, Thomas Hilgenberg, Willy |
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10.1111/j.1399-3054.1983.tb04185.x |
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