2012
DOI: 10.1016/j.carbpol.2011.12.041
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Characterization of ulvan extracts to assess the effect of different steps in the extraction procedure

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Cited by 89 publications
(47 citation statements)
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“…Characterization of the extracted polysaccharide revealed different physicochemical properties which are summarized in Table (adapted from Costa et al ., ).…”
Section: Methodsmentioning
confidence: 97%
“…Characterization of the extracted polysaccharide revealed different physicochemical properties which are summarized in Table (adapted from Costa et al ., ).…”
Section: Methodsmentioning
confidence: 97%
“…First, accurately determining the sugar composition of ulvans is difficult because the aldobiouronic linkage is refractory to acid hydrolysis and IdA is partially destroyed during acid hydrolysis. To minimize these effects, innovative methods combining mild acid hydrolysis with enzymatic degradation have been developed, and these techniques allow more accurate insights into the sugar composition of ulvans and authentication of the presence of IdA within the SP backbone [113,120,121]. Differences in species also contribute to the compositional variability of ulvans.…”
Section: Structural Diversity Of Green Algal Spsmentioning
confidence: 99%
“…These interesting features make ulvan an excellent candidate as a renewable and cheap compound for industrial purposes. Unfortunately its structure is difficult to define [7,40,41]. An enzymatic or chemical reduction of its molecular weight could lead to a more definable structure and improve the range of its activities, the efficiency and reduce the polydispersity of its molecular weight.…”
Section: Introductionmentioning
confidence: 99%
“…The genus Persicivirga has recently been merged in the genus Nonlabens [51] and the newly named Nonlabens ulvanivorans has been described to produce a β-glucuronyl hydrolase implicated in the degradation of ulvan [52]. Other authors have described the degradation of ulvan by enzymatic means but with alginate-degrading commercial enzymes or without further characterization of the bacteria used to obtain the enzyme [7,19,53]. The main challenge of enzymatic degradation is to maintain the basic structure of repetitive subunits with the sulfate functional groups while controlling the kinetics of degradation to obtain oligomers with a constant yield and molecular size.…”
Section: Introductionmentioning
confidence: 99%
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