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不动杆菌 BD4 和 BD413 的胞外多糖分布和生物乳化剂生产。

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

机构信息

Department of Microbiology, George S. Wise Faculty of Life Sciences, Tel Aviv University, Ramat Aviv, Israel.

出版信息

Appl Environ Microbiol. 1982 Dec;44(6):1335-41. doi: 10.1128/aem.44.6.1335-1341.1982.

Abstract

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.

摘要

高度包裹的鲍氏不动杆菌 BD4 和“微型包裹”一步突变体 A. calcoaceticus BD413 除了产生荚膜物质外,还产生了细胞外多糖。BD413 胞外多糖部分的鼠李糖与葡萄糖摩尔比(3:1)与荚膜物质的组成相似。在这两种菌株中,荚膜多糖的增加与细胞生长平行,并在静止期保持不变。胞外多糖从对数中期开始检测到,并在静止期开始后 5 到 8 小时继续在生长培养基中积累。BD413 菌株每细胞产生的总鼠李糖胞外多糖是 BD4 菌株的四分之一。根据生长培养基的不同,BD413 菌株产生的 32%至 63%的鼠李糖多糖是胞外的,而在 BD4 菌株中只有 7%至 14%是胞外的。在所有情况下,BD413 菌株产生的胞外鼠李糖多糖都多于 BD4 菌株。在葡萄糖培养基中,BD413 菌株产生的胞外乳化活性也比 BD4 菌株大约高出 10 倍。BD4 细胞剪切后获得的分离荚膜多糖没有乳化活性。因此,BD413 菌株要么产生了一种改良的胞外多糖,要么分泌了一种额外的物质,这种物质是其产生乳化活性的原因。由硫酸铵沉淀的 BD413 胞外乳化剂诱导的乳液需要镁离子和脂肪族和芳香族烃混合物的存在。

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