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氨基酸与甘氨酰-L-亮氨酸在猴小肠中的水解及转运的相互作用

Interaction of amino acids with glycl-L-leucine hydrolysis and transport in monkey small intestine.

作者信息

Ganapathy V, Radhakrishnan A N

出版信息

Clin Sci (Lond). 1979 Dec;57(6):521-7. doi: 10.1042/cs0570521.

Abstract
  1. There are two saturable transport processes in the monkey small intestine for glycyl-L-leucine, one with Vmax. 1 mumol min-1 g-1 wet weight of tissue and an affinity constant (kt) of 5 mmol/l, and the other with Vmax 3.9 mumol min-1 g-1 wet weight of tissue and kt 33 mmol/l. 2. Glycyl-L-leucine uptake is inhibited by a wide variety of amino acids, although to a variable extent. The inhibition was shown to be competitive with leucine used as the representative amino acid. Phenylalanine, methionine, alanine and leucine are the most potent in their inhibitory action. 3. The effect of various amino acids on the hydrolysis of glycyl-L-leucine by particulate and cytosol fractions of monkey small intestine was studied. All the amino acids, except glycine, proline, alanine and glutamic acid, inhibit both the particulate and cytosol glycyl-L-leucine hydrolase activities. In general, the cytosol enzyme is more susceptible to amino acid inhibition than the particulate enzyme. 4. There is no correlation between the effects of amino acids on glycyl-L-leucine uptake and hydrolysis of glycyl-L-leucine by either particulate or cytosol fraction.
摘要
  1. 猴小肠中存在两种甘氨酰-L-亮氨酸的可饱和转运过程,一种的最大转运速率(Vmax)为1 μmol·min⁻¹·g⁻¹组织湿重,亲和常数(kt)为5 mmol/L,另一种的Vmax为3.9 μmol·min⁻¹·g⁻¹组织湿重,kt为33 mmol/L。2. 甘氨酰-L-亮氨酸的摄取受到多种氨基酸的抑制,尽管抑制程度各不相同。已证明这种抑制与用作代表性氨基酸的亮氨酸存在竞争性。苯丙氨酸、蛋氨酸、丙氨酸和亮氨酸的抑制作用最强。3. 研究了各种氨基酸对猴小肠微粒体和胞质溶胶部分水解甘氨酰-L-亮氨酸的影响。除甘氨酸、脯氨酸、丙氨酸和谷氨酸外,所有氨基酸均抑制微粒体和胞质溶胶的甘氨酰-L-亮氨酸水解酶活性。一般来说,胞质溶胶酶比微粒体酶更容易受到氨基酸抑制。4. 氨基酸对甘氨酰-L-亮氨酸摄取的影响与微粒体或胞质溶胶部分对甘氨酰-L-亮氨酸的水解作用之间没有相关性。

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