Vaningelgem Frederik, Zamfir Medana, Mozzi Fernanda, Adriany Tom, Vancanneyt Marc, Swings Jean, De Vuyst Luc
Research Group of Industrial Microbiology, Fermentation Technology and Downstream Processing (IMDO), Department of Applied Biological Sciences, Vrije Universiteit Brussel (VUB), B-1050 Brussels, Belgium.
Appl Environ Microbiol. 2004 Feb;70(2):900-12. doi: 10.1128/AEM.70.2.900-912.2004.
Twenty-six lactic acid bacterium strains isolated from European dairy products were identified as Streptococcus thermophilus and characterized by bacterial growth and exopolysaccharide (EPS)-producing capacity in milk and enriched milk medium. In addition, the acidification rates of the different strains were compared with their milk clotting behaviors. The majority of the strains grew better when yeast extract and peptone were added to the milk medium, although the presence of interfering glucomannans was shown, making this medium unsuitable for EPS screening. EPS production was found to be strain dependent, with the majority of the strains producing between 20 and 100 mg of polymer dry mass per liter of fermented milk medium. Furthermore, no straightforward relationship between the apparent viscosity and EPS production could be detected in fermented milk medium. An analysis of the molecular masses of the isolated EPS by gel permeation chromatography revealed a large variety, ranging from 10 to >2,000 kDa. A distinction could be made between high-molecular-mass EPS (>1,000 kDa) and low-molecular-mass EPS (<1,000 kDa). Based on the molecular size of the EPS, three groups of EPS-producing strains were distinguished. Monomer analysis of the EPS by high-performance anion-exchange chromatography with amperometric detection was demonstrated to be a fast and simple method. All of the EPS from the S. thermophilus strains tested were classified into six groups according to their monomer compositions. Apart from galactose and glucose, other monomers, such as (N-acetyl)galactosamine, (N-acetyl)glucosamine, and rhamnose, were also found as repeating unit constituents. Three strains were found to produce EPS containing (N-acetyl)glucosamine, which to our knowledge was never found before in an EPS from S. thermophilus. Furthermore, within each group, differences in monomer ratios were observed, indicating possible novel EPS structures. Finally, large differences between the consistencies of EPS solutions from five different strains were assigned to differences in their molecular masses and structures.
从欧洲乳制品中分离出的26株乳酸菌被鉴定为嗜热链球菌,并通过在牛奶和强化牛奶培养基中的细菌生长及胞外多糖(EPS)产生能力进行了表征。此外,还比较了不同菌株的酸化速率与其凝乳行为。尽管添加酵母提取物和蛋白胨后多数菌株在牛奶培养基中生长得更好,但发现存在干扰性葡甘露聚糖,这使得该培养基不适用于EPS筛选。发现EPS产生具有菌株依赖性,多数菌株每升发酵牛奶培养基产生20至100毫克聚合物干质量的EPS。此外,在发酵牛奶培养基中未检测到表观粘度与EPS产生之间的直接关系。通过凝胶渗透色谱法对分离出的EPS的分子量进行分析,结果显示种类繁多,范围从10至>2000 kDa。可以区分高分子量EPS(>1000 kDa)和低分子量EPS(<1000 kDa)。基于EPS的分子大小,区分出三组EPS产生菌株。通过高效阴离子交换色谱-安培检测法对EPS进行单体分析被证明是一种快速简便的方法。根据其单体组成,测试的嗜热链球菌菌株的所有EPS都被分为六组。除了半乳糖和葡萄糖外,还发现其他单体,如(N-乙酰)半乳糖胺、(N-乙酰)葡萄糖胺和鼠李糖作为重复单元成分。发现三株菌株产生含有(N-乙酰)葡萄糖胺的EPS,据我们所知,此前从未在嗜热链球菌的EPS中发现过。此外,在每组中,观察到单体比例的差异,表明可能存在新型EPS结构。最后,来自五个不同菌株的EPS溶液的稠度差异很大,这归因于它们的分子量和结构差异。