1987
DOI: 10.1016/0008-6215(87)80124-6
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Structural Studies of an extracellular polysaccharide, S-657, elaborated by Xanthomonas ATCC 53159

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Cited by 39 publications
(15 citation statements)
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“…Although the primary structure of S-198 gum [60] is similar to that of gellan [43] [44], welan [55], rhamsan [56], S-657 [57] and S-88 [59] gum, its rheological characteristics differ from gellan (deacylated) [5], native gellan [6] and deacetylated rhamsan [12], but are essentially in agreement with those of welan [51], native rhamsan [52] [53], S-657 [54] and S-88 [58] gums. Thus, S-198 gum molecules may involve intramolecular associations, as do welan, rhamsan, S-657 and S-88 gum molecules.…”
Section: Discussionmentioning
confidence: 89%
See 1 more Smart Citation
“…Although the primary structure of S-198 gum [60] is similar to that of gellan [43] [44], welan [55], rhamsan [56], S-657 [57] and S-88 [59] gum, its rheological characteristics differ from gellan (deacylated) [5], native gellan [6] and deacetylated rhamsan [12], but are essentially in agreement with those of welan [51], native rhamsan [52] [53], S-657 [54] and S-88 [58] gums. Thus, S-198 gum molecules may involve intramolecular associations, as do welan, rhamsan, S-657 and S-88 gum molecules.…”
Section: Discussionmentioning
confidence: 89%
“…Intramolecular associations of rhamsan gum in aqueous solution. [56], and substitution at O-3 of every D-glucosyl residue next to the D-glucuronosyl residue by α-L-rhamnosyl disaccharide side-chains for S-657 gum [57]. The methyl groups of L-rhamnosyl residues played a dominant role in the thermal stability due to the formation of intramolecular van der Waals forces of attraction.…”
Section: Introductionmentioning
confidence: 99%
“…We have also proposed a model of intramolecular associations of welan 25 and S-657 26 gum, the structure of which is similar to that of gellan, but substituted at O-3 of every D-glucosyl residue next to the L-rhamnosyl residue by either -L-rhamnosyl or -L-mannosyl side chain in the ratio of 2:1 for the former, 27 and substituted at O-3 of every D-glucosyl residue next to the L-rhamnosyl residue by -L-rhamnosyl disaccharide side chains for the latter 28 in aqueous solution, as illustrated in Scheme 2 and Scheme 3. The intramolecular associations take place between the OH-4 of the D-glucosyl residue and the adjacent hemiacetal oxygen atom of the L-rhamnosyl residue with hydrogen bonding as in gellan gum and between the methyl group of the L-rhamnosyl residue and the adjacent hemiacetal oxygen atom of the D-glucosyl residue with van der Waals interaction.…”
Section: Yymentioning
confidence: 94%
“…This exopolysaccharide has been known to be produced by S. paucimobilis strain P4 (DSM 6418) (Lobas et al, 1994), a strain that was isolated by a selective culturing method (Lobas et al, 1992) from a culture of [P.] paucimobilis NCIB 11942 (Anson et al, 1987). Also of particular interest is the fact that PS-EDIV does not contain -mannose, which has been found as a constituent of sphingans S-130, S-88, S-198 and NW-11 (Jansson et al, 1985(Jansson et al, , 1986Chowdhury et al, 1987a ;Robison & Stipanovic, 1989). In addition, there is some similarity between exopolysaccharides produced by [P.] paucimobilis RMPD strains 17a and 17b (Hebbar et al, 1992).…”
Section: Discussionmentioning
confidence: 99%
“…Fredrickson et al, 1991Fredrickson et al, , 1995Harms et al, 1995 ;Karlson et al, 1995 ;Mueller et al, 1990 ;Nohynek et al, 1996a, b ;Wittich E. B. M. Denner and others et al, 1992 ;Zipper et al, 1996), as bacterial antagonists of phytopathogenic fungi (Berg & Balin, 1994) and for the production of industrially useful exopolysaccharides (Moorehouse, 1987 ;Chandrasekaran & Radha, 1995). Certain structurally related exopolysaccharides referred to as ' sphingans ' (Pollock, 1993) are synthesized by several Sphingomonas strains, and include the following : heteropolysaccharide S-7 (Kang & McNeely, 1976), gellan (S-60), S-88, welan (S-130) (Kang & Veeder, 1982a, b, 1985Kang et al, 1982 ;O'Neill et al, 1983), rhamsan (S-194) (Peik et al, 1983), S-198 (Peik et al, 1985), S-657 (Chowdhury et al, 1987b), NW11 (Robison & Stipanovic, 1989), PS-P4 (Lobas et al, 1994), GS-1 (Ashtaputre & Shah, 1995), I-886 (Falk et al, 1996) and HWR1 (Hashimoto & Murato, 1998). Sphingans share the same carbohydrate-backbone structure (-X-glucose-glucuronic acid-glucose-X-, where X is either -rhamnose or -mannose), to which distinct side-groups are attached, influencing their rheological properties.…”
Section: Abbreviationsmentioning
confidence: 99%