Alkali modification of carrageenans. Part V. the iota-nu hybrid carrageenan from Eucheuma denticulatum and its cyclization to iota-carrageenan
A homogeneous iota/nu-hybrid cairageenan (71% iota- and 21% nu-) isolated from Eucheuma denticulatum was used as a model compound to study the cyclization reaction of α-D-galactose 2,6-disulfate units to 3,6-anhydro-α-D- galactose 2-sulfate. The rate of cyclization, at 70°C, of this carrageenan is a...
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Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01448617_v58_n4_p455_Viana http://hdl.handle.net/20.500.12110/paper_01448617_v58_n4_p455_Viana |
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paper:paper_01448617_v58_n4_p455_Viana2023-06-08T15:12:09Z Alkali modification of carrageenans. Part V. the iota-nu hybrid carrageenan from Eucheuma denticulatum and its cyclization to iota-carrageenan Noseda, Miguel D. Cerezo, Alberto Saúl Alkaline treatment Cyclization rate Eucheuma denticulatum Iota-carrageenan Alkaline earth metals Degradation Enzyme kinetics Ethanol Seaweed Sol-gels Alkaline treatment Cyclization rate Eucheuma denticulatum Iota-carrageenan Alkali metals Eucheuma A homogeneous iota/nu-hybrid cairageenan (71% iota- and 21% nu-) isolated from Eucheuma denticulatum was used as a model compound to study the cyclization reaction of α-D-galactose 2,6-disulfate units to 3,6-anhydro-α-D- galactose 2-sulfate. The rate of cyclization, at 70°C, of this carrageenan is about 50 times faster than that of a porphyran (non-sulfated β-D-galactose linked to α-L-galactose 6-sulfate) and 210 times faster when compared with a lambda-carrageenan (2-sulfated β-D-units linked to α-D-galactose 2,6-disulfate). The use of this model compound confirms the previous hypothesis of the accelerating effect of the β-o-4-sulfate group as well as suggests the influence of the 2-sulfate of the α-D-galactose units on the 4C1 → 1C4 chair forms interchange. The easy of cyclization indicates that to produce commercial iota-carrageenans milder alkaline treatments could be used, avoiding degradation and increasing the gel strength. © 2004 Elsevier Ltd. All rights reserved. Fil:Noseda, M.D. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Cerezo, A.S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2004 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01448617_v58_n4_p455_Viana http://hdl.handle.net/20.500.12110/paper_01448617_v58_n4_p455_Viana |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
topic |
Alkaline treatment Cyclization rate Eucheuma denticulatum Iota-carrageenan Alkaline earth metals Degradation Enzyme kinetics Ethanol Seaweed Sol-gels Alkaline treatment Cyclization rate Eucheuma denticulatum Iota-carrageenan Alkali metals Eucheuma |
spellingShingle |
Alkaline treatment Cyclization rate Eucheuma denticulatum Iota-carrageenan Alkaline earth metals Degradation Enzyme kinetics Ethanol Seaweed Sol-gels Alkaline treatment Cyclization rate Eucheuma denticulatum Iota-carrageenan Alkali metals Eucheuma Noseda, Miguel D. Cerezo, Alberto Saúl Alkali modification of carrageenans. Part V. the iota-nu hybrid carrageenan from Eucheuma denticulatum and its cyclization to iota-carrageenan |
topic_facet |
Alkaline treatment Cyclization rate Eucheuma denticulatum Iota-carrageenan Alkaline earth metals Degradation Enzyme kinetics Ethanol Seaweed Sol-gels Alkaline treatment Cyclization rate Eucheuma denticulatum Iota-carrageenan Alkali metals Eucheuma |
description |
A homogeneous iota/nu-hybrid cairageenan (71% iota- and 21% nu-) isolated from Eucheuma denticulatum was used as a model compound to study the cyclization reaction of α-D-galactose 2,6-disulfate units to 3,6-anhydro-α-D- galactose 2-sulfate. The rate of cyclization, at 70°C, of this carrageenan is about 50 times faster than that of a porphyran (non-sulfated β-D-galactose linked to α-L-galactose 6-sulfate) and 210 times faster when compared with a lambda-carrageenan (2-sulfated β-D-units linked to α-D-galactose 2,6-disulfate). The use of this model compound confirms the previous hypothesis of the accelerating effect of the β-o-4-sulfate group as well as suggests the influence of the 2-sulfate of the α-D-galactose units on the 4C1 → 1C4 chair forms interchange. The easy of cyclization indicates that to produce commercial iota-carrageenans milder alkaline treatments could be used, avoiding degradation and increasing the gel strength. © 2004 Elsevier Ltd. All rights reserved. |
author |
Noseda, Miguel D. Cerezo, Alberto Saúl |
author_facet |
Noseda, Miguel D. Cerezo, Alberto Saúl |
author_sort |
Noseda, Miguel D. |
title |
Alkali modification of carrageenans. Part V. the iota-nu hybrid carrageenan from Eucheuma denticulatum and its cyclization to iota-carrageenan |
title_short |
Alkali modification of carrageenans. Part V. the iota-nu hybrid carrageenan from Eucheuma denticulatum and its cyclization to iota-carrageenan |
title_full |
Alkali modification of carrageenans. Part V. the iota-nu hybrid carrageenan from Eucheuma denticulatum and its cyclization to iota-carrageenan |
title_fullStr |
Alkali modification of carrageenans. Part V. the iota-nu hybrid carrageenan from Eucheuma denticulatum and its cyclization to iota-carrageenan |
title_full_unstemmed |
Alkali modification of carrageenans. Part V. the iota-nu hybrid carrageenan from Eucheuma denticulatum and its cyclization to iota-carrageenan |
title_sort |
alkali modification of carrageenans. part v. the iota-nu hybrid carrageenan from eucheuma denticulatum and its cyclization to iota-carrageenan |
publishDate |
2004 |
url |
https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01448617_v58_n4_p455_Viana http://hdl.handle.net/20.500.12110/paper_01448617_v58_n4_p455_Viana |
work_keys_str_mv |
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