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4,5-dihydroxy-2-oxo-6-phosphonooxy-hexanoic acid synthesis

2synthesis methods
-

Yield:-

Reaction Conditions:

with Saccharophagus degradans 2-40T 2-keto-3-deoxy-D-gluconate kinase;ATP in aq. buffer at 30; for 1 h;Enzymatic reaction;

Steps:



General procedure: To test enzyme activities of KDG kinase and KDPG aldolase in vitro, 800μg/mL of each purified enzyme were sequentially added to post-reaction mixtures that contained the corresponding substrates for the target enzymes. For the reaction by KDG kinase, 2.5mM of ATP was added in the reaction mixture as a phosphoryl donor. After incubating at 30°C for 1h, each enzymatic reaction mixture was quenched in boiling water for 5min. The production of KDPG by putative KDG kinase was confirmed by TLC and GC/MS, and the production of pyruvate by putative KDPG aldolase was confirmed by gas chromatography/time-of-flight mass spectrometry (GC/TOF MS).

References:

Kim, Do Hyoung;Wang, Damao;Yun, Eun Ju;Kim, Sooah;Kim, Soo Rin;Kim, Kyoung Heon [Process Biochemistry,2016,vol. 51,# 10,p. 1374 - 1379]