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Exopolysaccharide Distribution of and Bioemulsifier Production by Acinetobacter calcoaceticus BD4 and BD413

机译:钙不动杆菌BD4和BD413的胞外多糖分布和生物乳化剂的生产

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摘要

The heavily encapsulated Acinetobacter calcoaceticus BD4 and the “miniencapsulated” single-step mutant A. calcoaceticus BD413 produced extracellular polysaccharides in addition to the capsular material. The molar ratio of rhamnose to glucose (3:1) in the extracellular BD413 polysaccharide fraction was similar to the composition of the capsular material. In both strains, the increase in capsular polysaccharide was parallel to cell growth and remained constant in stationary phase. The extracellular polysaccharides were detected starting from mid-logarithmic phase and continued to accumulate in the growth medium for 5 to 8 h after the onset of stationary phase. Strain BD413 produced one-fourth the total rhamnose exopolysaccharide per cell that strain BD4 did. Depending on the growth medium, 32 to 63% of the rhamnose polysaccharide produced by strain BD413 was extracellular, whereas in strain BD4 only 7 to 14% was extracellular. In all cases, strain BD413 produced more extracellular rhamnose polysaccharide than strain BD4 did. In glucose medium, strain BD413 also produced approximately 10 times more extracellular emulsifying activity than strain BD4 did. The isolated capsular polysaccharide obtained after shearing of BD4 cells showed no emulsifying activity. Thus, strain BD413 either produces a modified extracellular polysaccharide or excretes an additional substance(s) that is responsible for the emulsifying activity. Emulsions induced by the ammonium sulfate-precipitated BD413 extracellular emulsifier require the presence of magnesium ion and a mixture of an aliphatic and an aromatic hydrocarbon.
机译:重包膜的钙不动杆菌不动杆菌BD4和“微囊化”的单步突变体A. calcoaceticus BD413除包膜材料外还产生细胞外多糖。胞外BD413多糖级分中鼠李糖与葡萄糖的摩尔比(3:1)与荚膜材料的组成相似。在两种菌株中,荚膜多糖的增加与细胞生长平行,在固定相中保持恒定。从对数中期开始检测到细胞外多糖,并在固定相开始后5到8 h继续在生长培养基中积累。 BD413菌株每个细胞产生的鼠李糖胞外多糖总量是BD4菌株的四分之一。取决于生长培养基,由菌株BD413产生的鼠李糖多糖的32%至63%在细胞外,而在菌株BD4中只有7%至14%在细胞外。在所有情况下,BD413菌株比BD4菌株产生更多的胞外鼠李糖多糖。在葡萄糖培养基中,菌株BD413产生的细胞外乳化活性也比菌株BD4高约10倍。剪切BD4细胞后获得的分离的荚膜多糖没有乳化活性。因此,菌株BD413要么产生修饰的细胞外多糖,要么排出负责乳化活性的另外的物质。由硫酸铵沉淀的BD413细胞外乳化剂诱导的乳液需要存在镁离子以及脂族和芳族烃的混合物。

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