2004
DOI: 10.1590/s1517-83822004000100026
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Comparison of two methods for purification of plantaricin ST31, a bacteriocin produced by Lactobacillus plantarum ST31

Abstract: Two methods of purification of the plantaricin ST31, a bacteriocin produced by Lactobacillus plantarum ST31 are used in this study -the method of ammonium sulfate precipitation, Sep-pack C 18 cartridge and reverse-phase HPLC chromatography on C 18 Nucleosil column, and the method of direct purification by cation exchange SP Sepharose Fast Flow column Amersham (Pharmacia Biotech). The purity of the products from the two experimental protocols are examined for their molecular weight, aminoacid composition and se… Show more

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Cited by 44 publications
(27 citation statements)
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“…at 100C, 121ᴼ C, -12ᴼ C, after which the bacteriocin activity was tested against methicillin resistance Staphylococcus aureus. The pH sensitivity of bacteriocinswere also determined at different pH by adjusting the pH of the extracted bacteriocins dissolved in buffer to 5,6,7,8,9, and 10. The inhibitory activity was detected by disc diffusion method [2].…”
Section: Heat and Ph Sensitivitymentioning
confidence: 99%
See 1 more Smart Citation
“…at 100C, 121ᴼ C, -12ᴼ C, after which the bacteriocin activity was tested against methicillin resistance Staphylococcus aureus. The pH sensitivity of bacteriocinswere also determined at different pH by adjusting the pH of the extracted bacteriocins dissolved in buffer to 5,6,7,8,9, and 10. The inhibitory activity was detected by disc diffusion method [2].…”
Section: Heat and Ph Sensitivitymentioning
confidence: 99%
“…The production of bacteriocinsdepend largely on the pH, source of nutrients and temperature [7]. Various physicochemical factors seemed to affect bacteriocin production as well as its activity.…”
Section: Introductionmentioning
confidence: 99%
“…Subsequently, several chromatographic steps including size exclusion (gel filtration), adsorbtion (ion-exchange), or hydrophobic interaction (reverse-phase) chromatography have been used to achieve significant purification of bacteriocins (Wu et al, 2004). Todorov et al, (2004) summarized the purification method used by others researchers as follow: (1) ammonium sulphate precipitation, and cation exchange-SP-sepharose, reversed-stationaryphase (octyl-sepharose-CL-4B), stationary-phase C2/C18 chromatography. (2) anion-exchange chromatography (DEAE-Sephadex A-25) and reversephase HPLC cation-exchange chromatography (SPsepharose fast-flow cation exchange column), C2/C18 reverse-phase chromatography and hydrophobic interaction chromatography (phenyl-sepharose CL-4B column) (3) ammonium sulphate precipitation (40%), and cation exchange-SP-sepharose (4) ammonium sulphate precipitation (55%), hydrophobic interaction (C8), cation exchange chromatography Mono S cation exchange column (phamacia, Biotech).…”
Section: Purification Of Lab Bacteriocinsmentioning
confidence: 99%
“…For example,nisin produced by several strains of Lactococcus lactis is the best known, most well characterized and the onlylantibiotic to have realized widespread commercial use. Lactobacillus plantarum produces serial bacteriocins likeplantaricin 35d, bacteriocins ST28MS and ST26MS that are active against the pathogens and spoilage microorganismsin foods (Todorov et al .,2004 and. Another bacteriocin has potential to be used in the food industry is pediocin which is an antilisterialbacteriocin produced by several Pediococcus strains.…”
Section: Potential Application Of Lab and Bacteriocins In The Food Inmentioning
confidence: 99%
“…The peptide remains active after incubation at pH 1 to 10 but is inactivated when treated with proteolytic enzymes including pepsin, papain, α-chymotrypsin, trypsin and Proteinase K. The mode of activity is bactericidal, as determined against Oenococcus oeni [4]. Several methods have been reported for the purification of plantaricins based on various combinations of ammonium sulphate precipitations, ion exchange, hydrophobic interaction and/or reversed-phase chromatography [4][5][6][7][8][9][10][11][12][13]. A rapid, two-step purification procedure using both cation-exchange chromatography and reverse-phase chromatography, enables purification of milligram quantities of pediocin-like bacteriocins and other cationic peptides [14].…”
Section: Introductionmentioning
confidence: 99%