Taxonomic group: fungi / Ascomycota
(Phylum: Ascomycota)
Host organism: Andrographis paniculata
The structure was elucidated in this paperNCBI PubMed ID: 26592702Publication DOI: 10.1016/j.ijbiomac.2015.11.035Journal NLM ID: 7909578Publisher: Butterworth-Heinemann
Correspondence: debu33

yahoo.com; db

mail.vidyasagar.ac.in; debu33

gmail.com
Institutions: Microbiology Laboratory, Department of Botany and Forestry, Vidyasagar University, Midnapore, West Bengal, India
There is a little information on exopolysaccharide production by endophytic fungi. In this investigation endophytic Pestalotiopsis sp. BC55 was used for optimization of exopolysaccharide production. One variable at a time method and response surface methodology were adopted to find out the best culture conditions and medium compositions for maximum exopolysaccharide production. The organism produced maximum exopolysaccharide (4.320 ± 0.022 g/l EPS) in 250 ml Erlenmeyer flask containing 75 ml potato dextrose broth supplemented with (g%/l) glucose, 7.66; urea, 0.29; CaCl2, 0.05 with medium pH 6.93; after 3.76 days of incubation at 24°C. Exopolysaccharide [EPS (EP-I)] produced by this organism have Mw ∼2×10(5)Da with a melting point range of 122-124°C. Structural elucidation of the EPS (PS-I) was carried out after a series of experiments. Result indicated the presence of only (1→3)-linked β-D-glucopyranosyl moiety. The structure of the repeating unit was established as →3)-β-D-Glcp-(1→.
characterization, exopolysaccharide, purification, optimization, endophytic Pestalotiopsis sp. BC55
Structure type: homopolymer ; 200000
Location inside paper: EPS, EP-1, p. 190 (right column), fig. 4
Compound class: EPS, glucan
Contained glycoepitopes: IEDB_1397514,IEDB_142488,IEDB_146664,IEDB_153543,IEDB_158555,IEDB_161166,IEDB_2278476,IEDB_2278477,IEDB_558869,IEDB_857743,IEDB_983931,SB_192
Methods: 13C NMR, 1H NMR, GLC-MS, gel filtration, DNA techniques, GLC, paper chromatography, FTIR, electron microscopy, optical rotation measurement, acetylation, methylation analysis, melting point determination, TFA hydrolysis
Biosynthesis and genetic data: genetic data
NCBI Taxonomy refs (TaxIDs): 1325273Reference(s) to other database(s): GTC:G51056AN
Show glycosyltransferases
NMR conditions: in DMSO-d6 at 300 K
[as TSV]
13C NMR data:
Linkage Residue C1 C2 C3 C4 C5 C6
bDGlcp 103.1 73.1 84.9 69.2 75.5 61.2
1H NMR data:
Linkage Residue H1 H2 H3 H4 H5 H6
bDGlcp 4.5 3.04 3.63 3.10 3.52 3.80-3.88
1H/13C HSQC data:
Linkage Residue C1/H1 C2/H2 C3/H3 C4/H4 C5/H5 C6/H6
bDGlcp 103.1/4.5 73.1/3.04 84.9/3.63 69.2/3.10 75.5/3.52 61.2/3.80-3.88
1H NMR data:
| Linkage | Residue | H1 | H2 | H3 | H4 | H5 | H6 |
| | bDGlcp | 4.5 | 3.04 | 3.63 | 3.10 | 3.52 | 3.80 3.88 |
|
13C NMR data:
| Linkage | Residue | C1 | C2 | C3 | C4 | C5 | C6 |
| | bDGlcp | 103.1 | 73.1 | 84.9 | 69.2 | 75.5 | 61.2 |
|
There is only one chemically distinct structure: