Cyanohydrin glycosides of Passiflora: distribution pattern, a saturated cyclopentane derivative from P. guatemalensis, and formation of pseudocyanogenic alpha-hydroxyamides as isolation artefacts

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Cyanohydrin glycosides of Passiflora : distribution pattern, a saturated cyclopentane derivative from P. guatemalensis, and formation of pseudocyanogenic alpha-hydroxyamides as isolation artefacts. / Jaroszewski, Jerzy W; Olafsdottir, Elin S; Wellendorph, Petrine; Christensen, Jette Lynggaard; Franzyk, Henrik; Somanadhan, Brinda; Budnik, Bogdan A; Jørgensen, Lise Bolt; Clausen, Vicki.

In: Phytochemistry, Vol. 59, No. 5, 2002, p. 501-11.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Jaroszewski, JW, Olafsdottir, ES, Wellendorph, P, Christensen, JL, Franzyk, H, Somanadhan, B, Budnik, BA, Jørgensen, LB & Clausen, V 2002, 'Cyanohydrin glycosides of Passiflora: distribution pattern, a saturated cyclopentane derivative from P. guatemalensis, and formation of pseudocyanogenic alpha-hydroxyamides as isolation artefacts', Phytochemistry, vol. 59, no. 5, pp. 501-11.

APA

Jaroszewski, J. W., Olafsdottir, E. S., Wellendorph, P., Christensen, J. L., Franzyk, H., Somanadhan, B., Budnik, B. A., Jørgensen, L. B., & Clausen, V. (2002). Cyanohydrin glycosides of Passiflora: distribution pattern, a saturated cyclopentane derivative from P. guatemalensis, and formation of pseudocyanogenic alpha-hydroxyamides as isolation artefacts. Phytochemistry, 59(5), 501-11.

Vancouver

Jaroszewski JW, Olafsdottir ES, Wellendorph P, Christensen JL, Franzyk H, Somanadhan B et al. Cyanohydrin glycosides of Passiflora: distribution pattern, a saturated cyclopentane derivative from P. guatemalensis, and formation of pseudocyanogenic alpha-hydroxyamides as isolation artefacts. Phytochemistry. 2002;59(5):501-11.

Author

Jaroszewski, Jerzy W ; Olafsdottir, Elin S ; Wellendorph, Petrine ; Christensen, Jette Lynggaard ; Franzyk, Henrik ; Somanadhan, Brinda ; Budnik, Bogdan A ; Jørgensen, Lise Bolt ; Clausen, Vicki. / Cyanohydrin glycosides of Passiflora : distribution pattern, a saturated cyclopentane derivative from P. guatemalensis, and formation of pseudocyanogenic alpha-hydroxyamides as isolation artefacts. In: Phytochemistry. 2002 ; Vol. 59, No. 5. pp. 501-11.

Bibtex

@article{08d1ec99e463475a85b5e4bdce9500c6,
title = "Cyanohydrin glycosides of Passiflora: distribution pattern, a saturated cyclopentane derivative from P. guatemalensis, and formation of pseudocyanogenic alpha-hydroxyamides as isolation artefacts",
abstract = "Nineteen species of Passiflora (Passifloraceae) were examined for the presence of cyanogenic glycosides. Passibiflorin, a bisglycoside containing the 6-deoxy-beta-D-gulopyranosyl residue, was isolated from P. apetala, P. biflora, P. cuneata, P. indecora, P. murucuja and P. perfoliata. In some cases this glycoside co-occurs with simple beta-D-glucopyranosides: tetraphyllin A, deidaclin, tetraphyllin B, volkenin, epivolkenin and taraktophyllin. P. citrina contains passicapsin, a rare glycoside with the 2,6-dideoxy-beta-D-xylo-hexopyranosyl moiety, while P. herbertiana contains tetraphyllin A, deidaclin, epivolkenin and taraktophyllin, P. discophora tetraphyllin B and volkenin, and P. x violacea tetraphyllin B sulfate. The remaining species were noncyanogenic. The glycosides were identified by 1H and 13C NMR spectroscopy following isolation by reversed-phase preparative HPLC. From P. guatemalensis, a new glucoside named passiguatemalin was isolated and identified as a 1-(beta-D-glucopyranosyloxy)-2,3-dihydroxycyclopentane-1-carbonitrile. An isomeric glycoside was prepared by catalytic hydrogenation of gynocardin. alpha-Hydroxyamides corresponding to the cyanogenic glycosides were isolated from several Passiflora species. These alpha-hydroxyamides, presumably formed during processing of the plant material, behave as cyanogenic compounds when treated with commercial Helix pomatia crude enzyme preparation. Thus, the enzyme preparation appears to contain an amide dehydratase, which converts alpha-hydroxyamides to cyanohydrins that liberate cyanide; this finding is of interest in connection with analysis of plant tissues and extracts using Helix pomatia enzymes.",
keywords = "Amides, Chromatography, High Pressure Liquid, Glycosides, Magnetic Resonance Spectroscopy, Nitriles, Passiflora",
author = "Jaroszewski, {Jerzy W} and Olafsdottir, {Elin S} and Petrine Wellendorph and Christensen, {Jette Lynggaard} and Henrik Franzyk and Brinda Somanadhan and Budnik, {Bogdan A} and J{\o}rgensen, {Lise Bolt} and Vicki Clausen",
year = "2002",
language = "English",
volume = "59",
pages = "501--11",
journal = "Phytochemistry",
issn = "0031-9422",
publisher = "Pergamon Press",
number = "5",

}

RIS

TY - JOUR

T1 - Cyanohydrin glycosides of Passiflora

T2 - distribution pattern, a saturated cyclopentane derivative from P. guatemalensis, and formation of pseudocyanogenic alpha-hydroxyamides as isolation artefacts

AU - Jaroszewski, Jerzy W

AU - Olafsdottir, Elin S

AU - Wellendorph, Petrine

AU - Christensen, Jette Lynggaard

AU - Franzyk, Henrik

AU - Somanadhan, Brinda

AU - Budnik, Bogdan A

AU - Jørgensen, Lise Bolt

AU - Clausen, Vicki

PY - 2002

Y1 - 2002

N2 - Nineteen species of Passiflora (Passifloraceae) were examined for the presence of cyanogenic glycosides. Passibiflorin, a bisglycoside containing the 6-deoxy-beta-D-gulopyranosyl residue, was isolated from P. apetala, P. biflora, P. cuneata, P. indecora, P. murucuja and P. perfoliata. In some cases this glycoside co-occurs with simple beta-D-glucopyranosides: tetraphyllin A, deidaclin, tetraphyllin B, volkenin, epivolkenin and taraktophyllin. P. citrina contains passicapsin, a rare glycoside with the 2,6-dideoxy-beta-D-xylo-hexopyranosyl moiety, while P. herbertiana contains tetraphyllin A, deidaclin, epivolkenin and taraktophyllin, P. discophora tetraphyllin B and volkenin, and P. x violacea tetraphyllin B sulfate. The remaining species were noncyanogenic. The glycosides were identified by 1H and 13C NMR spectroscopy following isolation by reversed-phase preparative HPLC. From P. guatemalensis, a new glucoside named passiguatemalin was isolated and identified as a 1-(beta-D-glucopyranosyloxy)-2,3-dihydroxycyclopentane-1-carbonitrile. An isomeric glycoside was prepared by catalytic hydrogenation of gynocardin. alpha-Hydroxyamides corresponding to the cyanogenic glycosides were isolated from several Passiflora species. These alpha-hydroxyamides, presumably formed during processing of the plant material, behave as cyanogenic compounds when treated with commercial Helix pomatia crude enzyme preparation. Thus, the enzyme preparation appears to contain an amide dehydratase, which converts alpha-hydroxyamides to cyanohydrins that liberate cyanide; this finding is of interest in connection with analysis of plant tissues and extracts using Helix pomatia enzymes.

AB - Nineteen species of Passiflora (Passifloraceae) were examined for the presence of cyanogenic glycosides. Passibiflorin, a bisglycoside containing the 6-deoxy-beta-D-gulopyranosyl residue, was isolated from P. apetala, P. biflora, P. cuneata, P. indecora, P. murucuja and P. perfoliata. In some cases this glycoside co-occurs with simple beta-D-glucopyranosides: tetraphyllin A, deidaclin, tetraphyllin B, volkenin, epivolkenin and taraktophyllin. P. citrina contains passicapsin, a rare glycoside with the 2,6-dideoxy-beta-D-xylo-hexopyranosyl moiety, while P. herbertiana contains tetraphyllin A, deidaclin, epivolkenin and taraktophyllin, P. discophora tetraphyllin B and volkenin, and P. x violacea tetraphyllin B sulfate. The remaining species were noncyanogenic. The glycosides were identified by 1H and 13C NMR spectroscopy following isolation by reversed-phase preparative HPLC. From P. guatemalensis, a new glucoside named passiguatemalin was isolated and identified as a 1-(beta-D-glucopyranosyloxy)-2,3-dihydroxycyclopentane-1-carbonitrile. An isomeric glycoside was prepared by catalytic hydrogenation of gynocardin. alpha-Hydroxyamides corresponding to the cyanogenic glycosides were isolated from several Passiflora species. These alpha-hydroxyamides, presumably formed during processing of the plant material, behave as cyanogenic compounds when treated with commercial Helix pomatia crude enzyme preparation. Thus, the enzyme preparation appears to contain an amide dehydratase, which converts alpha-hydroxyamides to cyanohydrins that liberate cyanide; this finding is of interest in connection with analysis of plant tissues and extracts using Helix pomatia enzymes.

KW - Amides

KW - Chromatography, High Pressure Liquid

KW - Glycosides

KW - Magnetic Resonance Spectroscopy

KW - Nitriles

KW - Passiflora

M3 - Journal article

C2 - 11853745

VL - 59

SP - 501

EP - 511

JO - Phytochemistry

JF - Phytochemistry

SN - 0031-9422

IS - 5

ER -

ID: 42406147