2001
DOI: 10.1007/s002530000497
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Studies on the possibility of histidine biosynthesis from histidinol, imidazolepyruvic acid, imidazoleacetic acid, and imidazolelactic acid by mixed ruminal bacteria, protozoa, and their mixture in vitro

Abstract: The possibility of histidine (His) synthesis using a main biosynthetic pathway involving histidinol (HDL) and also the recycling capability of imidazolic compounds such as imidazolepyruvic acid (ImPA), imidazoleacetic acid (ImAA), and imidazolelactic acid (ImLA) to produce His were investigated using mixed ruminal bacteria (B), protozoa (P), and a mixture of both (BP) in an in vitro system. Rumen microorganisms were anaerobically incubated at 39 degrees C for 18 h with or without each substrate (2 mM) mentione… Show more

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Cited by 6 publications
(6 citation statements)
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“…Imidazole lactic acid is one of the metabolites of histidine (Wadud, Onodera, & Or-Rashid, 2001). In mammals, histidine can be metabolized to imidazole lactic acid, imidazole pyruvic acid and imidazole acetic acid, and these metabolites can be excreted through the urine (Block, Westhoff, & Steele, 1967).…”
Section: Discussionmentioning
confidence: 99%
“…Imidazole lactic acid is one of the metabolites of histidine (Wadud, Onodera, & Or-Rashid, 2001). In mammals, histidine can be metabolized to imidazole lactic acid, imidazole pyruvic acid and imidazole acetic acid, and these metabolites can be excreted through the urine (Block, Westhoff, & Steele, 1967).…”
Section: Discussionmentioning
confidence: 99%
“…histidine, histidinol, urocanic acid and imidazolepyruvic acid) in rumen fluid were performed under two different chromatographic conditions on a Lichrospher 100 NH 2 column (Wadud et al, 2000(Wadud et al, , 2001. The mobile-phase for the isocratic elution in the first chromatographic condition was 67 mM potassium phosphate (pH 6.45) and 90% acetonitrile in water (21:79), while an acetonitrile gradient in 63 mM potassium phosphate (pH 3.0), prepared by the addition of 60 mM phosphoric acid, was used for the second system.…”
Section: Application Of Lc To Biological Specimensmentioning
confidence: 99%
“…In order to prove the above hypothesis, enzymatic experiment was conducted in the author's laboratory as reported recently (Wadud et al, 2001b). Namely, histidinol dehydrogenase (HLDase) (EC 1.1.1.23), which catalyzes the reaction from histidinol to histidine at the final step of the histidine de novo synthetic pathway as mentioned above, was chosen to be examined with cattle liver and kidney, since in any case it is necessary to know at first the enzyme activity of the final step of the system as has been tested for proving the ability of histidine synthesis in rumen microorganisms (Wadud et al 2001a). HLDase activity was assayed by determining increase in histidine with crude enzyme solution prepared from liver and kidney collected from Japanese black cattle (delivered cattle) immediately after slaughter.…”
Section: Histidinol Dehydrogenase In Ruminantsmentioning
confidence: 99%
“…(partly cited from Wadud et al 2001a) in younger animals, while production of histidine may increase in proportion to growing stages, if the HLDase activity per unit weight of tissue does not vary largely with growth. Therefore, it is considered that the relationship between production and requirement (supply and demand) of histidine vary with growing stages.…”
Section: Histidinol Dehydrogenase In Ruminantsmentioning
confidence: 99%
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