Taxonomic group: bacteria / Proteobacteria
(Phylum: Proteobacteria)
Associated disease: infection due to Enterobacter cloacae [ICD11:
XN3YM 
]
The structure was elucidated in this paperNCBI PubMed ID: 29804997Publication DOI: 10.1016/j.carbpol.2018.04.114Journal NLM ID: 8307156Publisher: Elsevier
Correspondence: lj2388240

gdmu.edu.cn; Jun Liu <liujungdmedical

gmail.com>
Institutions: Laboratory of Pathogenic Biology, Guangdong Medical University, Zhanjiang, Guangdong 524023, China
In this study, a polysaccharide (ECP) was isolated from the mycelium of Enterobacter cloacae and was found to exhibit strong antibacterial activities against E. cloacae producing SHV-12 ESBL with the increase of the inhibition zone diameter. Its minimum inhibitory concentration (MIC) and minimal bactericidal concentration (MBC) were 12.5 mg/L and 25 mg/L, respectively. ECP at these concentrations immediately inhibited planktonic growth of the bacteria especially at the time from 2 to 10 h. Flow cytometry analysis further revealed that almost all the bacterial cells were damaged following ECP treatment. The permeability of the cytoplasmic membrane of E. cloacae was increased when ECP concentrations increasing, as evidenced by an influx of Na and an efflux of K, P or S, the leakage of intracellular ATP and the UV-absorbing substances, as well as the depolarization of the cytoplasmic membrane, indicating that bactericidal activity of ECP was achieved by inducing cell membrane damage.
structural analysis, Enterobacter cloacae, Antibacterial mechanism, Antibacterial polysaccharide, SHV-12 extended-spectrum beta-lactamase
Structure type: polymer chemical repeating unit ; 105000
Location inside paper: p.447, table 2
Trivial name: ECP
Contained glycoepitopes: IEDB_141806,IEDB_142488,IEDB_146664,IEDB_241101,IEDB_983931,SB_192
Methods: 13C NMR, 1H NMR, methylation, PCR, GC-MS, anion-exchange chromatography, GC, FTIR, composition analysis, UV, statistical analysis, antibacterial assay, flow cytometry
Biological activity: ECP against E. cloacae (12.5 mg/L (MIC) and 25 mg/L (MBC)), immediately inhibited planktonic growth of the bacteria. A most strong bacterial killing effect happened at about 4-6 h.
NCBI Taxonomy refs (TaxIDs): 550Reference(s) to other database(s): GTC:G22616AK
Show glycosyltransferases
NMR conditions: in D2O at 323 K
[as TSV]
13C NMR data:
Linkage Residue C1 C2 C3 C4 C5 C6
4 bDGlcp 103.42 73.86 75.98 70.02 74.85 68.54
bDGlcp 104.12 73.54 75.19 79.82 75.91 62.27
1H NMR data:
Linkage Residue H1 H2 H3 H4 H5 H6
4 bDGlcp 4.45 3.35 3.51 3.48 3.56 3.85-4.11
bDGlcp 4.56 3.45 3.70 3.69 3.58 3.70-3.81
1H/13C HSQC data:
Linkage Residue C1/H1 C2/H2 C3/H3 C4/H4 C5/H5 C6/H6
4 bDGlcp 103.42/4.45 73.86/3.35 75.98/3.51 70.02/3.48 74.85/3.56 68.54/3.85-4.11
bDGlcp 104.12/4.56 73.54/3.45 75.19/3.70 79.82/3.69 75.91/3.58 62.27/3.70-3.81
1H NMR data:
| Linkage | Residue | H1 | H2 | H3 | H4 | H5 | H6 |
| 4 | bDGlcp | 4.45 | 3.35 | 3.51 | 3.48 | 3.56 | 3.85 4.11 |
| | bDGlcp | 4.56 | 3.45 | 3.70 | 3.69 | 3.58 | 3.70 3.81 |
|
13C NMR data:
| Linkage | Residue | C1 | C2 | C3 | C4 | C5 | C6 |
| 4 | bDGlcp | 103.42 | 73.86 | 75.98 | 70.02 | 74.85 | 68.54 |
| | bDGlcp | 104.12 | 73.54 | 75.19 | 79.82 | 75.91 | 62.27 |
|
There is only one chemically distinct structure: