Aureobasidium pullulans as a source of liamocins (heavy oils) with anticancer activity

被引:43
|
作者
Manitchotpisit, Pennapa [1 ]
Watanapoksin, Ramida [2 ]
Price, Neil P. J. [3 ]
Bischoff, Kenneth M. [3 ]
Tayeh, Malatee [2 ]
Teeraworawit, Sudarat [1 ]
Kriwong, Saranya [1 ]
Leathers, Timothy D. [3 ]
机构
[1] Rangsit Univ, Fac Sci, Dept Med Sci, Lakhok 12000, Pathumthani, Thailand
[2] Srinakharinwirot Univ, Dept Biochem, Fac Med, Bangkok 10110, Thailand
[3] ARS, Renewable Prod Technol Res Unit, Natl Ctr Agr Utilizat Res, USDA, Peoria, IL 61604 USA
来源
关键词
Anticancer agents; Aureobasidium pullulans; Liamocins; Phylogeny; Pullulan; 5-HYDROXY-2-DECENOYL ESTERS; POLYOL LIPIDS; MANNITOL; 3,5-DIHYDROXYDECANOYL; ARABITOL;
D O I
10.1007/s11274-014-1639-7
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Liamocins are structurally unique, heavier-than-water "oils" produced by certain strains of Aureobasidium pullulans. The aim of the current study is to identify new sources of liamocins and evaluate their potential as anticancer agents. Nine strains of A. pullulans from phylogenetic clades 8, 9, and 11 were examined for the first time for production of liamocins. Strains in these clades have only been isolated from tropical environments, and all strains tested here were from various locations in Thailand. Strains RSU 9, RSU 21, and RSU 29, all from clade 11, produced from 7.0 to 8.6 g liamocins/l from medium containing 5 % sucrose. These are the highest yields of liamocins that we have found thus far. These strains also produced from 9.4 to 17 g pullulan/l. The structural identity of liamocins was confirmed by matrix-assisted laser desorption/ionization mass spectrometry; differential spectra were obtained in which the dominant ion was either at about m/z 805.5 or m/z 949.6, consistent with the structure of liamocins. Liamocins from A. pullulans strains RSU 9 and RSU 21 inhibited two human breast cancer cell lines and a human cervical cancer cell line (IC50 values of 32.2 +/- A 1.4 to 63.1 +/- A 2.4 mu g liamocins/ml) but were not toxic to a normal cell line. Liamocins weakly inhibited a strain of Enterococcus faecalis, but did not inhibit strains of Lactobacillus fermentum, Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa. Thus, A. pullulans phylogenetic clade 11 is a promising source of liamocins, and these compounds merit further examination as potential anticancer agents.
引用
收藏
页码:2199 / 2204
页数:6
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