1932
DOI: 10.1038/129795b0
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Feeding Experiments with Methionine

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Cited by 17 publications
(6 citation statements)
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“…Cysteine is a component of keratin and other fibrous proteins, and typically has a lower digestibility (Kerr et al, 2014). One must consider the low digestibility of cysteine (range from 50.22% to 68.37% in present study) and low methionine DIAAS-like value for chicken meal (78.10) when formulating diets, especially when using meals that have undergone rendering and drying processes due to the fact that cysteine is supported by the metabolism of methionine (Weichselbaum et al, 1932). If an ingredient has a low cysteine digestibility plus a methionine DIAAS-like value that does not meet 100%, supplementation of methionine or cysteine may be required to prevent deficiency.…”
Section: Discussionmentioning
confidence: 90%
“…Cysteine is a component of keratin and other fibrous proteins, and typically has a lower digestibility (Kerr et al, 2014). One must consider the low digestibility of cysteine (range from 50.22% to 68.37% in present study) and low methionine DIAAS-like value for chicken meal (78.10) when formulating diets, especially when using meals that have undergone rendering and drying processes due to the fact that cysteine is supported by the metabolism of methionine (Weichselbaum et al, 1932). If an ingredient has a low cysteine digestibility plus a methionine DIAAS-like value that does not meet 100%, supplementation of methionine or cysteine may be required to prevent deficiency.…”
Section: Discussionmentioning
confidence: 90%
“…The effect of injecting methionine on wool growth was studied because, from observations of Jackson and Block (6) and Weichselbaum, Weichselbaum and Stewart (33), it might be inferred that cystine and methionine are interconvertible in metabolism. They found that the growth of rats upon the Sherman-Merrill diet was increased on the addition of methionine to their ration.…”
Section: Discussionmentioning
confidence: 99%
“…Zum Antigen-Nachweis mit Hilfe der Immunfluoreszenz sind Tupfpräparate und Ausstriche von den Organen infizierter Tiere auf Objektträgern angefertigt worden. Diese Präparate wurden nach kurzer Lufttrocknung 10 Minuten lang in Aceton fixiert und, sofern sie nicht sofort weiter bearbeitet wurden, bei -20° C aufbewahrt. Für Giemsa-Färbungen verwendeten wir luftgetrocknete und Methanol-fixierte Präparate, Untersuchungen von Blut infizierter Tiere erfolgten anfänglich auf dün-nen Objektträger-Ausstrichen, später in dicken Tropfen", die nach Hämolyse und Lufttrocknung mit Aceton fixiert wurden.…”
Section: Materials Und Methodenunclassified