Obtaining and determination of the concentration in the culture fluid of phaecin – peptide bacteriocin Enterococcus faecium

Bacteriology ◽  
2020 ◽  
Vol 5 (4) ◽  
pp. 20-24
Author(s):  
V.M. Borzenkov ◽  
◽  
V.P. Levchuk ◽  
V.I. Surovtsev ◽  
◽  
...  

Phaecin, a peptide bacteriocin with a molecular mass of ~5 kDa, was obtained and purified to an electrophoretically pure state with a yield of ~70% of the total activity in the culture fluid. The method of time-of-flight mass spectrometry (MALDI) showed that bacteriocin consists of two components A and B with similar molecular mass. In previously published works, the yield of purified bacteriocins, usually did not exceed 4–5% of the total activity in the culture fluid. The authors believe that the increase in yield is due to the fact that not only the similarity of bacteriocins with high molecular mass proteins was taken into account, but also differences associated with low molecular mass, the ability to hydrophobic interaction at slightly alkaline pH values and resistance to denaturation. Using the Scopes method, it was possible to determine the concentration of phaecin in the final stage of purification and in the culture fluid in absolute units (mg/l). The methods of the purification with high yield described in this work are probably applicable to other bacteriocins due to the proximity of their physicochemical properties. Key words: Enterococcus faecium, Listeria monocytogenes, bacteriocin, phaecin, culture liquid, adsorption chromatography, Scopes equation

2018 ◽  
pp. 138-146 ◽  
Author(s):  
Karin Abraham ◽  
Eckhard Flöter

The presence of polysaccharides in cane and beet raw juices causes several negative effects during the sugar manufacture. These are usually mitigated by enzymatic decomposition of dextrans. Such effects not only depend on the content, but also on the molecular mass distribution. This means that the different dextran fractions specifically affect the process. An accurate process control hence requires the most precise knowledge about the existing content and the molecular mass distribution present. A detailed understanding of the specific processing problems and also a targeted enzyme application hence requires the determination of a total dextran content and also its characterization including the differentiation between the different dextran fractions. An accurate analytical tool which equally satisfies industrial applicability is still lacking. To improve on this situation, two new approaches for the determination of dextran were developed and benchmarked against the commonly used and established Haze Method, which is rather inaccurate and also sensitive to molecular mass variation. The two new approaches are both based on polarimetry. These two methods indicate to be superior over the Haze Method with respect two molecular mass variation and hence enable the determination of a broader molecular size range including also low molecular mass dextrans.


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