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- W2470674295 abstract "Publisher Summary This chapter discusses the determination of 4-deoxy-L-threo-5-hexosulose uronic acid isomerase. The most convenient assay for the isomerization of compound I (4-deoxy-L- threo -5-hexosulose uronic acid) to compound II (3-deoxy-D- glycero -2,5-hexodmlosonic acid) proved to be the spectrophotometric determination of the reduction of the latter by reduced diphosphopyridine nucleotide (DPNH) at 340 mμ in the presence of an excess of 3-deoxy-D- glycero -2,5-hexodiulosonic acid reductase. One unit is defined as that amount of enzyme required to catalyze the isomerization of 1 micromole of compound (I) in 1 minute. Specific activity is defined as units of enzyme per milligram of protein. The isomerase reaction proceeds with maximal velocity in phosphate buffer in the narrow range of pH 7.0–7.5. In phosphate buffer, pH 7.0, the equilibrium ratio of compound (II) to compound (I) was found to be about 1.1:1.0. In borate buffer, pH 8.0, the equilibrium ratio of compound (II) to compound (I) was about 2.7." @default.
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- W2470674295 date "1966-01-01" @default.
- W2470674295 modified "2023-09-27" @default.
- W2470674295 title "[107] 4-Deoxy-l-threo-5-hexosulose uronic acid isomerase" @default.
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- W2470674295 doi "https://doi.org/10.1016/0076-6879(66)09121-3" @default.
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