Linamarin - The toxic compound of cassava

Detalhes bibliográficos
Autor(a) principal: Cereda, M. P. [UNESP]
Data de Publicação: 1996
Outros Autores: Mattos, M. C Y [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1590/S0104-79301996000100002
http://hdl.handle.net/11449/64711
Resumo: Cassava is a widely grown root crop which accumulates two cyanogenic glucosides, linamarin and lotaustralin. Linamarin accounts for more than 80% of the cassava cyanogenic glucosides. It is a β-glucoside of acetone cyanohydrin and ethyl-methyl-ketone-cyanohydrin. Linamarin β-linkage can only be broken under high pressure, high temperature and use of mineral acids, while its enzymatic break occurs easily. Linamarase, an endogenous cassava enzyme, can break this β-linkage. The enzymatic reaction occurs under optimum conditions at 25°C, at pH 5.5 to 6.0. Linamarin is present in all parts of the cassava plant, being more concentrated on the root and leaves. If the enzyme and substrate are joined, a good detoxification can occur. All the cassava plant species are known to contain cyanide. Toxicity caused by free cyanide (CN-) has already been reported, while toxicity caused by glucoside has not. The lethal dose of CN- is 1 mg/kg of live weight; hence, cassava root classification into toxic and non-toxic depending on the amount of cyanide in the root. Should the cyanide content be high enough to exceed such a dose, the root is regarded as toxic. Values from 15 to 400 ppm (mg CN-/kg of fresh weight) of hydrocyanic acid in cassava roots have been mentioned in the literature. However, more frequent values in the interval 30 to 150 ppm have been observed. Processed cassava food consumed in Brazil is safe in regard to cyanide toxicity.
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spelling Linamarin - The toxic compound of cassavacassavaculinary and industrial usescyanidecyanogenic glucosidelinamarinresidueswaste waterhydrogen cyanidedetoxificationfood safetyhumannonhumanplant rootshort surveyCassava is a widely grown root crop which accumulates two cyanogenic glucosides, linamarin and lotaustralin. Linamarin accounts for more than 80% of the cassava cyanogenic glucosides. It is a β-glucoside of acetone cyanohydrin and ethyl-methyl-ketone-cyanohydrin. Linamarin β-linkage can only be broken under high pressure, high temperature and use of mineral acids, while its enzymatic break occurs easily. Linamarase, an endogenous cassava enzyme, can break this β-linkage. The enzymatic reaction occurs under optimum conditions at 25°C, at pH 5.5 to 6.0. Linamarin is present in all parts of the cassava plant, being more concentrated on the root and leaves. If the enzyme and substrate are joined, a good detoxification can occur. All the cassava plant species are known to contain cyanide. Toxicity caused by free cyanide (CN-) has already been reported, while toxicity caused by glucoside has not. The lethal dose of CN- is 1 mg/kg of live weight; hence, cassava root classification into toxic and non-toxic depending on the amount of cyanide in the root. Should the cyanide content be high enough to exceed such a dose, the root is regarded as toxic. Values from 15 to 400 ppm (mg CN-/kg of fresh weight) of hydrocyanic acid in cassava roots have been mentioned in the literature. However, more frequent values in the interval 30 to 150 ppm have been observed. Processed cassava food consumed in Brazil is safe in regard to cyanide toxicity.CERAT-UNESP Center of Tropical Roots Sao Paulo State University, Caixa Postal 237, CEP 18603-970 Botucatu, Sao PauloCERAT-UNESP Center of Tropical Roots Sao Paulo State University, Caixa Postal 237, CEP 18603-970 Botucatu, Sao PauloUniversidade Estadual Paulista (Unesp)Cereda, M. P. [UNESP]Mattos, M. C Y [UNESP]2014-05-27T11:18:03Z2014-05-27T11:18:03Z1996-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article6-12http://dx.doi.org/10.1590/S0104-79301996000100002Journal of Venomous Animals and Toxins, v. 2, n. 1, p. 6-12, 1996.0104-7930http://hdl.handle.net/11449/6471110.1590/S0104-79301996000100002S0104-793019960001000022-s2.0-0030003530Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Venomous Animals and Toxinsinfo:eu-repo/semantics/openAccess2024-04-12T13:49:52Zoai:repositorio.unesp.br:11449/64711Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T23:38:01.500772Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Linamarin - The toxic compound of cassava
title Linamarin - The toxic compound of cassava
spellingShingle Linamarin - The toxic compound of cassava
Cereda, M. P. [UNESP]
cassava
culinary and industrial uses
cyanide
cyanogenic glucoside
linamarin
residues
waste water
hydrogen cyanide
detoxification
food safety
human
nonhuman
plant root
short survey
title_short Linamarin - The toxic compound of cassava
title_full Linamarin - The toxic compound of cassava
title_fullStr Linamarin - The toxic compound of cassava
title_full_unstemmed Linamarin - The toxic compound of cassava
title_sort Linamarin - The toxic compound of cassava
author Cereda, M. P. [UNESP]
author_facet Cereda, M. P. [UNESP]
Mattos, M. C Y [UNESP]
author_role author
author2 Mattos, M. C Y [UNESP]
author2_role author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Cereda, M. P. [UNESP]
Mattos, M. C Y [UNESP]
dc.subject.por.fl_str_mv cassava
culinary and industrial uses
cyanide
cyanogenic glucoside
linamarin
residues
waste water
hydrogen cyanide
detoxification
food safety
human
nonhuman
plant root
short survey
topic cassava
culinary and industrial uses
cyanide
cyanogenic glucoside
linamarin
residues
waste water
hydrogen cyanide
detoxification
food safety
human
nonhuman
plant root
short survey
description Cassava is a widely grown root crop which accumulates two cyanogenic glucosides, linamarin and lotaustralin. Linamarin accounts for more than 80% of the cassava cyanogenic glucosides. It is a β-glucoside of acetone cyanohydrin and ethyl-methyl-ketone-cyanohydrin. Linamarin β-linkage can only be broken under high pressure, high temperature and use of mineral acids, while its enzymatic break occurs easily. Linamarase, an endogenous cassava enzyme, can break this β-linkage. The enzymatic reaction occurs under optimum conditions at 25°C, at pH 5.5 to 6.0. Linamarin is present in all parts of the cassava plant, being more concentrated on the root and leaves. If the enzyme and substrate are joined, a good detoxification can occur. All the cassava plant species are known to contain cyanide. Toxicity caused by free cyanide (CN-) has already been reported, while toxicity caused by glucoside has not. The lethal dose of CN- is 1 mg/kg of live weight; hence, cassava root classification into toxic and non-toxic depending on the amount of cyanide in the root. Should the cyanide content be high enough to exceed such a dose, the root is regarded as toxic. Values from 15 to 400 ppm (mg CN-/kg of fresh weight) of hydrocyanic acid in cassava roots have been mentioned in the literature. However, more frequent values in the interval 30 to 150 ppm have been observed. Processed cassava food consumed in Brazil is safe in regard to cyanide toxicity.
publishDate 1996
dc.date.none.fl_str_mv 1996-01-01
2014-05-27T11:18:03Z
2014-05-27T11:18:03Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1590/S0104-79301996000100002
Journal of Venomous Animals and Toxins, v. 2, n. 1, p. 6-12, 1996.
0104-7930
http://hdl.handle.net/11449/64711
10.1590/S0104-79301996000100002
S0104-79301996000100002
2-s2.0-0030003530
url http://dx.doi.org/10.1590/S0104-79301996000100002
http://hdl.handle.net/11449/64711
identifier_str_mv Journal of Venomous Animals and Toxins, v. 2, n. 1, p. 6-12, 1996.
0104-7930
10.1590/S0104-79301996000100002
S0104-79301996000100002
2-s2.0-0030003530
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Venomous Animals and Toxins
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 6-12
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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