Biopolymers Online 2002
DOI: 10.1002/3527600035.bpol5010
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Sphingan Group of Exopolysaccharides (EPS)

Abstract: Introduction Historical Outline Chemical Structures Structural Variations Analytical Methods Occurrence Physiology Properties Biosynthesis Synthesis of Sugar‐nucleotide Substrates … Show more

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Cited by 9 publications
(8 citation statements)
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“…Apparently, they are not effective on Sphingomonas sp. and their EPSs as might be expected from the physicochemical properties of the components involved (Balkwill w a t e r r e s e a r c h 4 5 ( 2 0 1 1 ) 4 0 5 e4 1 6 et al, Denner et al, 2001;Pollock, 2002). The study of the unique EPSs and glycosphingolipids of sphingomonads species might result in the development of more effective and directed cleaning methods to control biofouling.…”
Section: Chemical Treatment Is Not Cleaningmentioning
confidence: 99%
“…Apparently, they are not effective on Sphingomonas sp. and their EPSs as might be expected from the physicochemical properties of the components involved (Balkwill w a t e r r e s e a r c h 4 5 ( 2 0 1 1 ) 4 0 5 e4 1 6 et al, Denner et al, 2001;Pollock, 2002). The study of the unique EPSs and glycosphingolipids of sphingomonads species might result in the development of more effective and directed cleaning methods to control biofouling.…”
Section: Chemical Treatment Is Not Cleaningmentioning
confidence: 99%
“…However, a polysaccharide with both acidic residues has never been described before. The substitution of glucuronic acid and deoxyglucuronic acid in the third position might occur through the same mechanism as that for the change of rhamnose and mannose in the first position in S-88 or S-198, where the substituents are distributed statistically at a ratio of 1:1 (Pollock, 2002), or in welan, where a similar substitution in the side chain is observed. Possibly, the substitution of the hydroxyl group in position 2 from GlcA to 2dGlcA might be analogous to the separation mechanism of the hydroxyl group in position 6 from mannose to rhamnose.…”
Section: Matrix-assisted Laser Desorption/ionization-time-of-flight Mmentioning
confidence: 98%
“…They usually consist of a linear repeating tetrasaccharide containing rhamnose, glucose, mannose and glucuronic acid in differing proportions and frequency, and with distinct side chains, e.g., glycosidic bound glucose or rhamnose (Pollock 2002).…”
Section: Introductionmentioning
confidence: 99%
“…Moreover, they are used in pharmaceutical/biomedical [19,20], cosmetic [21], chemical [22,23] and food industries [24,25]. …”
Section: Introductionmentioning
confidence: 99%