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Selection of effective methods for extracting extracellular polymeric substances (EPSs) from Bacillus megaterium TF10

机译:从巨大芽孢杆菌TF10提取细胞外聚合物的有效方法的选择

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Bacterial extracellular polymeric substances (EPSs) play an important role in the formation and stabilization of bioaggregates, such as biofilm, microbial flocs and granules. Thus, the selection of appropriate extraction method is of critical importance, which may affect the yield, compositions and properties of EPS. In this work, six different methods used for EPS extraction, including ultrasonication, heating, formaldehyde + NaOH, H2SO4, glutaraldehyde, and EDTA methods, from Bacillus megaterium TF10, a bacterium with a high EPS-producing capacity isolated from a soil sample, are investigated. These EPS extraction methods are compared in terms of EPS yields and compositions, cell lysis, and flocculation activities and spectrum characteristics of extracted EPS. The results show that both EPS yield and cell lysis generally increase with the extraction time. The heating, formaldehyde + NaOH and H2SO4 methods lead to a high EPS yield compared to the ultrasonication or EDTA methods, while the ultrasonication and H2SO4 methods cause much more cell lysis than the formaldehyde + NaOH treatment. The flocculation activities of EPS, which can quantitatively reflect the EPS disruption during extraction, are also evaluated. The flocculation efficiencies of the extracted EPS are found in the order of: formaldehyde + NaOH (30-min formaldehyde treatment and then 60-min NaOH treatment), 92.4% > EDTA (10 h), 92.2% > heating (120 min), 91.6% > glutaraldehyde (15 min), 90.9% > ultrasonication (30 min), 81.0% > H2SO4 (45 min), 73.2% > control, 59.9%. The IR and EEM spectra suggest that the EPS compositions and structures also vary significantly with the extraction method. Among the six methods, the EDTA method with an extraction time of 10 h was identified to be most effective method to extract EPS from B. megaterium TF10.
机译:细菌细胞外聚合物质(EPS)在生物聚集体(例如生物膜,微生物絮凝物和颗粒)的形成和稳定中起着重要作用。因此,选择合适的提取方法至关重要,这可能会影响EPS的收率,组成和性能。在这项工作中,从巨大芽孢杆菌TF10(一种从土壤样品中分离出来的具有高EPS产生能力的细菌)中提取了六种不同的EPS提取方法,包括超声处理,加热,甲醛+ NaOH,H2SO4,戊二醛和EDTA方法。调查。比较了这些EPS提取方法的EPS产量和组成,细胞裂解以及所提取EPS的絮凝活性和光谱特征。结果表明,EPS的产量和细胞裂解通常随提取时间的增加而增加。与超声或EDTA方法相比,加热,甲醛+ NaOH和H2SO4方法可提高EPS产量,而超声和H2SO4方法比甲醛+ NaOH处理可导致更多的细胞裂解。还评估了EPS的絮凝活性,该活性可以定量反映萃取过程中EPS的破坏。提取到的EPS的絮凝效率依次为:甲醛+ NaOH(30分钟甲醛处理,然后60分钟NaOH处理),92.4%> EDTA(10小时),92.2%>加热(120分钟), 91.6%>戊二醛(15分钟),90.9%>超声处理(30分钟),81.0%> H2SO4(45分钟),73.2%>对照,59.9%。 IR和EEM光谱表明,EPS的组成和结构也随着萃取方法的不同而显着变化。在这六种方法中,提取时间为10 h的EDTA方法被认为是从巨大芽孢杆菌TF10中提取EPS的最有效方法。

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