Cytotoxicity activities and chemical characteristics of exopolysaccharides and intracellular polysaccharides of Physarum polycephalum microplasmodia.
Cytotoxicity
HeLa
MCF-7
Microplasmodia
Physarum polycephalum
Polysaccharides
Journal
BMC biotechnology
ISSN: 1472-6750
Titre abrégé: BMC Biotechnol
Pays: England
ID NLM: 101088663
Informations de publication
Date de publication:
27 03 2021
27 03 2021
Historique:
received:
20
10
2020
accepted:
15
03
2021
entrez:
28
3
2021
pubmed:
29
3
2021
medline:
29
12
2021
Statut:
epublish
Résumé
Microbial polysaccharides have been reported to possess remarkable bioactivities. Physarum polycephalum is a species of slime mold for which the microplasmodia are capable of rapid growth and can produce a significant amount of cell wall-less biomass. There has been a limited understanding of the polysaccharides produced by microplasmodia of slime molds, including P. polycephalum. Thus, the primary objectives of this research were first to chemically characterize the exopolysaccharides (EPS) and intracellular polysaccharides (IPS) of P. polycephalum microplasmodia and then to evaluate their cytotoxicity against several cancer cell lines. The yields of the crude EPS (4.43 ± 0.44 g/l) and partially purified (deproteinated) EPS (2.95 ± 0.85 g/l) were comparable (p > 0.05) with the respective crude IPS (3.46 ± 0.36 g/l) and partially purified IPS (2.45 ± 0.36 g/l). The average molecular weight of the EPS and IPS were 14,762 kDa and 1788 kDa. The major monomer of the EPS was galactose (80.22%), while that of the IPS was glucose (84.46%). Both crude and purified IPS samples showed significantly higher cytotoxicity toward Hela cells, especially the purified sample and none of the IPSs inhibited normal cells. Only 38.42 ± 2.84% Hela cells remained viable when treated with the partially purified IPS (1 mg/ml). However, although only 34.76 ± 6.58% MCF-7 cells were viable when exposed to the crude IPS, but the partially purified IPS displayed non-toxicity to MCF-7 cells. This suggested that the cytotoxicity toward MCF-7 would come from some component associated with the crude IPS sample (e.g. proteins, peptides or ion metals) and the purification process would have either completely removed or reduced amount of that component. Cell cycle analysis by flow cytometry suggested that the mechanism of the toxicity of the crude IPS toward MCF-7 and the partially purified IPS toward Hela cells was due to apoptosis. The EPS and IPS of P. polycephalum microplasmodia had different chemical properties including carbohydrate, protein and total sulfate group contents, monosaccharide composition and molecular weights, which led to different cytotoxicity activities. The crude and partially purified IPSs would be potential materials for further study relating to cancer treatment.
Sections du résumé
BACKGROUND
Microbial polysaccharides have been reported to possess remarkable bioactivities. Physarum polycephalum is a species of slime mold for which the microplasmodia are capable of rapid growth and can produce a significant amount of cell wall-less biomass. There has been a limited understanding of the polysaccharides produced by microplasmodia of slime molds, including P. polycephalum. Thus, the primary objectives of this research were first to chemically characterize the exopolysaccharides (EPS) and intracellular polysaccharides (IPS) of P. polycephalum microplasmodia and then to evaluate their cytotoxicity against several cancer cell lines.
RESULTS
The yields of the crude EPS (4.43 ± 0.44 g/l) and partially purified (deproteinated) EPS (2.95 ± 0.85 g/l) were comparable (p > 0.05) with the respective crude IPS (3.46 ± 0.36 g/l) and partially purified IPS (2.45 ± 0.36 g/l). The average molecular weight of the EPS and IPS were 14,762 kDa and 1788 kDa. The major monomer of the EPS was galactose (80.22%), while that of the IPS was glucose (84.46%). Both crude and purified IPS samples showed significantly higher cytotoxicity toward Hela cells, especially the purified sample and none of the IPSs inhibited normal cells. Only 38.42 ± 2.84% Hela cells remained viable when treated with the partially purified IPS (1 mg/ml). However, although only 34.76 ± 6.58% MCF-7 cells were viable when exposed to the crude IPS, but the partially purified IPS displayed non-toxicity to MCF-7 cells. This suggested that the cytotoxicity toward MCF-7 would come from some component associated with the crude IPS sample (e.g. proteins, peptides or ion metals) and the purification process would have either completely removed or reduced amount of that component. Cell cycle analysis by flow cytometry suggested that the mechanism of the toxicity of the crude IPS toward MCF-7 and the partially purified IPS toward Hela cells was due to apoptosis.
CONCLUSIONS
The EPS and IPS of P. polycephalum microplasmodia had different chemical properties including carbohydrate, protein and total sulfate group contents, monosaccharide composition and molecular weights, which led to different cytotoxicity activities. The crude and partially purified IPSs would be potential materials for further study relating to cancer treatment.
Identifiants
pubmed: 33773573
doi: 10.1186/s12896-021-00688-5
pii: 10.1186/s12896-021-00688-5
pmc: PMC8005236
doi:
Substances chimiques
Antineoplastic Agents
0
Polysaccharides
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
28Références
Int J Biol Macromol. 2013 Nov;62:13-7
pubmed: 23973493
Carbohydr Res. 2003 Jul 4;338(14):1517-21
pubmed: 12829397
Adv Biomed Res. 2018 Oct 24;7:132
pubmed: 30464932
Carbohydr Res. 2009 Nov 2;344(16):2209-16
pubmed: 19733344
Carbohydr Polym. 2014 Oct 13;111:245-55
pubmed: 25037349
Mutat Res. 2011 Apr 3;721(2):157-62
pubmed: 21262385
Carbohydr Polym. 2013 Aug 14;97(1):177-87
pubmed: 23769535
Materials (Basel). 2019 May 07;12(9):
pubmed: 31067636
N Engl J Med. 1998 Sep 24;339(13):900-5
pubmed: 9744975
J Bacteriol. 1970 Dec;104(3):1110-8
pubmed: 16559083
Carbohydr Res. 2007 Dec 10;342(17):2611-8
pubmed: 17868661
Carbohydr Res. 2003 Nov 21;338(24):2835-40
pubmed: 14667704
Cytobios. 1977;20(79-80):163-77
pubmed: 104827
Carbohydr Polym. 2012 Nov 6;90(4):1395-410
pubmed: 22944395
Biotechnol Prog. 2019 Nov;35(6):e2873
pubmed: 31215765
Anal Biochem. 1976 May 7;72:248-54
pubmed: 942051
Int J Biol Macromol. 2016 Dec;93(Pt A):226-234
pubmed: 27543344
Carbohydr Polym. 2015 Apr 20;120:102-14
pubmed: 25662693
Carbohydr Res. 2016 Apr 7;424:30-41
pubmed: 26974354
Food Chem Toxicol. 2009 Jan;47(1):1-8
pubmed: 18672018
BMC Complement Altern Med. 2016 Jul 16;16:220
pubmed: 27421261
BMC Biotechnol. 2017 Nov 09;17(1):76
pubmed: 29121887
Microb Cell Fact. 2018 Feb 21;17(1):29
pubmed: 29466981
Bioresour Technol. 2008 Jan;99(1):76-82
pubmed: 17306976
Carbohydr Polym. 2014 Jan;99:226-34
pubmed: 24274500
Bioresour Technol. 2007 Jan;98(2):395-401
pubmed: 16459075
Biol Pharm Bull. 2002 Jul;25(7):931-9
pubmed: 12132673
Nat Protoc. 2006;1(3):1458-61
pubmed: 17406435
Int J Biol Macromol. 2015 Mar;74:119-26
pubmed: 25532782
Carbohydr Polym. 2017 Sep 1;171:307-315
pubmed: 28578968
Bioresour Technol. 2006 Oct;97(15):1822-7
pubmed: 16256343
Anal Biochem. 1969 Nov;32(2):314-21
pubmed: 5396941
J Gen Microbiol. 1961 May;25:47-59
pubmed: 13719600
FEBS Lett. 1970 Mar 16;7(1):80-82
pubmed: 11947436