Research output: Contribution to journal › Article › peer-review
Determination of native amino acids and lactic acid in Lactobacillus helveticus culture media by capillary electrophoresis using Cu2+ and β-cyclodextrins as additives. / Makeeva, Daria ; Polikarpova, Daria ; Demyanova, Elena ; Roshchina, Evgeniia ; Vakhitov, Timur ; Kartsova, Liudmila .
In: Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences, Vol. 1156, 122304, 11.2020.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Determination of native amino acids and lactic acid in Lactobacillus helveticus culture media by capillary electrophoresis using Cu2+ and β-cyclodextrins as additives
AU - Makeeva, Daria
AU - Polikarpova, Daria
AU - Demyanova, Elena
AU - Roshchina, Evgeniia
AU - Vakhitov, Timur
AU - Kartsova, Liudmila
N1 - Publisher Copyright: © 2020 Elsevier B.V.
PY - 2020/11
Y1 - 2020/11
N2 - A capillary electrophoresis method for selective simultaneous determination and quantitation of native amino acids and lactic acid during cultivation of Lactobacillus helveticus D75 and D76 strains on the MRS-1 and milk nutrient media was presented. The method provided sensitive UV-detection of native analytes with minimum sample preparation and appeared to be extremely useful for the analysis of culture media. Native amino acids and lactic acid were separated and detected as complexes with Cu2+ ions, while proposed application of β-cyclodextrin (β-CD) and its charged and uncharged derivates (sulfated β-CD and 2-hydroxypropyl-β-CD) as pseudo stationary phases provided better separation selectivity. The effect of CDs, Cu2+, sodium acetate, β-CDs concentrations and pH of background electrolyte (BGE) on the electrophoretic mobilities of AAs was thoroughly investigated. The composition of the BGE was found to be as follows: 20 mM acetate buffer solution, 50 mM CuSO4, 10 mM 2-hydroxypropyl-β-CD, pH 4.3. The developed method possessed high analysis-to-analysis and day-to-day repeatability of migration times (RSD ≤ 1.0% and ≤ 2.5%, respectively). The differences in production of amino acids by D75 and D76 strains grown together and separately were found and concluded to be a consequence and/or one of the causes of synergism and syntropy of the strains. The developed method proved to be applicable for the analysis of culture media.
AB - A capillary electrophoresis method for selective simultaneous determination and quantitation of native amino acids and lactic acid during cultivation of Lactobacillus helveticus D75 and D76 strains on the MRS-1 and milk nutrient media was presented. The method provided sensitive UV-detection of native analytes with minimum sample preparation and appeared to be extremely useful for the analysis of culture media. Native amino acids and lactic acid were separated and detected as complexes with Cu2+ ions, while proposed application of β-cyclodextrin (β-CD) and its charged and uncharged derivates (sulfated β-CD and 2-hydroxypropyl-β-CD) as pseudo stationary phases provided better separation selectivity. The effect of CDs, Cu2+, sodium acetate, β-CDs concentrations and pH of background electrolyte (BGE) on the electrophoretic mobilities of AAs was thoroughly investigated. The composition of the BGE was found to be as follows: 20 mM acetate buffer solution, 50 mM CuSO4, 10 mM 2-hydroxypropyl-β-CD, pH 4.3. The developed method possessed high analysis-to-analysis and day-to-day repeatability of migration times (RSD ≤ 1.0% and ≤ 2.5%, respectively). The differences in production of amino acids by D75 and D76 strains grown together and separately were found and concluded to be a consequence and/or one of the causes of synergism and syntropy of the strains. The developed method proved to be applicable for the analysis of culture media.
KW - amino acids
KW - Lactic acid
KW - Capillary electrophoresis
KW - Culture medium
KW - Lactobacillus helveticus
KW - β-cyclodextrin
KW - Amino acids
UR - https://www.sciencedirect.com/science/article/pii/S1570023220308308#!
UR - http://www.scopus.com/inward/record.url?scp=85089541390&partnerID=8YFLogxK
U2 - 10.1016/j.jchromb.2020.122304
DO - 10.1016/j.jchromb.2020.122304
M3 - Article
VL - 1156
JO - Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences
JF - Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences
SN - 1570-0232
M1 - 122304
ER -
ID: 62023557