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- W1457515607 abstract "Cellulose-synthesizing cells of A. xylinum previously grown on succinate are cultivated in the following medium prepared with glass-distilled water: succinic acid, 2%; yeast extract (Difco) 0.5%; Bacto peptone (Difco), 0.5%; and monopotassium phosphate, 0.3%. The final pH is adjusted to 4.0 with NaOH. The contents of the flask are shaken vigorously to enhance the release of the cells embedded in the surface pellicle in the medium. Activity of the enzyme both in its particulate and soluble forms is significantly stimulated by monovalent anions in the following order: NO-> Br- > C1- > CN- > CH-COO-. Oxidation of malate is 60% inhibited by citrate or malonate at concentration equal to that of the substrate, whereas m-tartrate, DL-tartrate, and isocitrate are inhibitory only when present at a higher concentration. Other microorganisms are reported to contain nicotinamide nucleotide-independent enzyme systems capable of oxidizing L-malate to oxaloacetate. In addition to A. xylinum, these systems are demonstrated in Micrococcus lysodeikticus, Mycobacterium avium, Mycobacterium phlei, Pseudomonas ovalis Chester, and Azotobacter vinelandii." @default.
- W1457515607 created "2016-06-24" @default.
- W1457515607 creator A5014071370 @default.
- W1457515607 date "1969-01-01" @default.
- W1457515607 modified "2023-10-13" @default.
- W1457515607 title "[22] Malate dehydrogenase (FAD-linked) from Acetobacter xylinum" @default.
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- W1457515607 doi "https://doi.org/10.1016/0076-6879(69)13026-8" @default.
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