Liang Tzu-Wen, Tseng Shih-Chun, Wang San-Lang
Life Science Development Center, Tamkang University, No. 151, Yingchuan Rd., Tamsui, New Taipei City 25137, Taiwan.
Department of Chemistry, Tamkang University, New Taipei City 25137, Taiwan.
Mar Drugs. 2016 Feb 19;14(2):40. doi: 10.3390/md14020040.
Natural polysaccharides have received much attention due to their wide range of applications. Although most microbial exopolysaccharides (EPSs) use sugars as the major carbon source, such as glucose or sucrose, in this study, EPSs were induced from a squid pen powder (SPP)-containing medium by Paenibacillus mucilaginosus TKU032, a bacterial strain isolated from Taiwanese soil. Under the optimal culture conditions, the maximum EPS yield (14.8 g/L) was obtained. MALDI-TOF MS analysis of an EPS fraction purified by gel filtration revealed two mass peaks with molecular weights of ∼1.05 × 10⁴ and ∼1.35 × 10⁴ Da, respectively. The analysis of the hydrolysates of TKU032 EPS with cellulase, pectinase or α-amylase indicated that the glycosidic bond of TKU032 EPS is most likely an α-1,4 glycosidic bond and the hydrolysates are similar to those of starch. In addition, the purified EPS demonstrated strong antioxidant abilities.
天然多糖因其广泛的应用而备受关注。尽管大多数微生物胞外多糖(EPSs)以糖类作为主要碳源,如葡萄糖或蔗糖,但在本研究中,台湾土壤分离的芽孢杆菌Paenibacillus mucilaginosus TKU032从含鱿鱼笔粉(SPP)的培养基中诱导产生了EPSs。在最佳培养条件下,获得了最大EPS产量(14.8 g/L)。对通过凝胶过滤纯化的EPS组分进行的基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)分析显示,有两个质量峰,分子量分别约为1.05×10⁴和1.35×10⁴ Da。用纤维素酶、果胶酶或α-淀粉酶对TKU032 EPS的水解产物进行分析表明,TKU032 EPS的糖苷键很可能是α-1,4糖苷键,且水解产物与淀粉的水解产物相似。此外,纯化后的EPS表现出较强的抗氧化能力。