Taxonomic group: bacteria / Firmicutes
(Phylum: Firmicutes)
NCBI PubMed ID: 39547628Publication DOI: 10.1016/j.ijbiomac.2024.137623Journal NLM ID: 7909578Publisher: Butterworth-Heinemann
Correspondence: grinev

ibppm.ru
Institutions: Institute of Biochemistry and Physiology of Plants and Microorganisms, Saratov Scientific Centre of the Russian Academy of Sciences (IBPPM RAS), Saratov, Russia, Chernyshevsky Saratov State University, Saratov, Russia, VIC Animal Health, VIC GROUP, Belgorod, Russia, Perm State University, Perm, Russia
Levan-type polysaccharides, produced by various organisms, are nontoxic, biocompatible, and biodegradable polymers with a wide range of biological activities. They have high potential for use in medicine, cosmetology, and industry. A large amount of levan (41.1 g L-1) was recovered by ethanol precipitation from a liquid nutrient medium of Paenibacillus polymyxa 88A that contained 15 % w/v sucrose as a carbon source. The levan was fractionated by gel-permeation and anion-exchange chromatography and was analyzed by DRIFT and NMR spectroscopy. It was found that levan was represented by slightly branched chains composed of β-(2→6)-Fruf residues. The average molecular mass of the levan was about 1.9 MDa. When shear stress was applied at different temperatures, aqueous levan solutions showed pseudoplastic behavior. As found by SEM, a freeze-dried powdered levan sample had a microporous structure. The levan had excellent emulsifying activity toward sunflower oil, forming an emulsion with long-term stability. Analysis of the antioxidant activity of the levan showed a higher, dose-dependent activity toward ABTS, as compared with that toward DPPH. Finally, the bioactivity of the levan was examined by MTT assay by using human cervical carcinoma (HeLa) cells
Rheology, levan, antitumor activity, thermal stability, Paenibacillus polymyxa, emulsifying activity
Structure type: homopolymer
Location inside paper: pg. 6, Table 1
Trivial name: levan, levan-type polysaccharide
Compound class: EPS, polysaccharide, fructan
Contained glycoepitopes: IEDB_923066
Methods: acid hydrolysis, anion-exchange chromatography, biological assays, MS, HPAEC-PAD, extraction, HPGPC, precipitation, spectrophotometry, SEM, centrifugation, AFM, TGA, DSC, FT-IR, cell viability, rheological studies, antioxidant activity test
NCBI Taxonomy refs (TaxIDs): 1406Reference(s) to other database(s): GTC:G29465PK, GlycomeDB:
9593
Show glycosyltransferases
NMR conditions: in D2O / TSP at 303 K
[as TSV]
13C NMR data:
Linkage Residue C1 C2 C3 C4 C5 C6
bDFruf 61.7 105.3 77.5 76.5 81.6 64.7
1H NMR data:
Linkage Residue H1 H2 H3 H4 H5 H6
bDFruf 3.65-3.76 - 4.18 4.08 3.94 3.54-3.89
1H/13C HSQC data:
Linkage Residue C1/H1 C2/H2 C3/H3 C4/H4 C5/H5 C6/H6
bDFruf 61.7/3.65-3.76 77.5/4.18 76.5/4.08 81.6/3.94 64.7/3.54-3.89
1H NMR data:
Linkage | Residue | H1 | H2 | H3 | H4 | H5 | H6 |
| bDFruf | 3.65 3.76 |
| 4.18 | 4.08 | 3.94 | 3.54 3.89 |
|
13C NMR data:
Linkage | Residue | C1 | C2 | C3 | C4 | C5 | C6 |
| bDFruf | 61.7 | 105.3 | 77.5 | 76.5 | 81.6 | 64.7 |
|
There is only one chemically distinct structure: