Simonian A L, Rainina E I, Lozinsky V I, Badalian I E, Khachatrian G E, Tatikian S Sh, Makhlis T A, Varfolomeyev S D
Yerevan Physics Institute, Armenia.
Appl Biochem Biotechnol. 1992 Sep;36(3):199-210. doi: 10.1007/BF02921779.
A biosensor to quantify L-proline within 10(-5)-10(-3) mole/L concentration is described. Immobilized Pseudomonas sp. cells grown in a medium containing L-proline as the only source of carbon and nitrogen were used to create the biosensor. The cells oxidized L-proline specifically consuming O2 and did not react with other amino acids and sugars. The change in oxygen concentration was detected with a Clark oxygen membrane electrode. The cells were immobilized by entrapment in polyvinyl alcohol (PVA) cryogel. The resultant biocatalyst had a high mechanical strength and retained its L-proline-oxidizing ability for at least two months.
本文描述了一种用于定量检测浓度在10⁻⁵ - 10⁻³摩尔/升范围内L-脯氨酸的生物传感器。将在含有L-脯氨酸作为唯一碳源和氮源的培养基中生长的固定化假单胞菌属细胞用于构建该生物传感器。这些细胞特异性地氧化L-脯氨酸并消耗氧气,且不与其他氨基酸和糖类发生反应。通过克拉克氧膜电极检测氧气浓度的变化。细胞通过包埋在聚乙烯醇(PVA)冷冻凝胶中进行固定。所得的生物催化剂具有较高的机械强度,并且其L-脯氨酸氧化能力至少可保持两个月。