从大鼠肝脏分离的高纯度过氧化物酶体中不同链长脂肪酸的β -氧化速率和不饱和程度

David S. Chance, Michael K. McIntosh
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引用次数: 6

摘要

从未经处理的大鼠肝脏中获得高度纯化的过氧化物酶体,并使用不同链长和不饱和程度的脂肪酰基辅酶a测量过氧化物酶体β -氧化率。通过标记酶过氧化氢酶和尿酸氧化酶的特异活性,从粗肝脏匀浆中采用差速离心技术和30% Nycodenz梯度分离获得了20 - 24倍的过氧化物酶体纯化。在纯化的最后一步中使用30%的Nycodenz梯度在去除溶酶体污染方面非常有效(例如减少5.5倍)。以月桂酰辅酶a (C12:0)为底物的过氧化物酶体β -氧化率是所有测试的脂肪酰基辅酶a中最高的。纯化过氧化物酶体不能氧化丁基辅酶a (C4:0)。一般来说,当脂肪酰基辅酶a的链长超过12个碳时,β -氧化速率降低。
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Rates of beta-oxidation of fatty acids of various chain lengths and degrees of unsaturation in highly purified peroxisomes isolated from rat liver

Highly purified peroxisomes were obtained from the liver of untreated rats, and rates of peroxisomal beta-oxidation were measured using fatty acyl-CoAs differing in chain length and degree of unsaturation. A 20–24-fold purification of peroxisomes, indicated by the specific activities of the marker enzymes catalase and urate oxidase, respectively, was obtained from crude liver homogenate using differential centrifugation techniques followed by a 30% Nycodenz gradient separation. The use of a 30% Nycodenz gradient in the final step of purification was extremely effective (e.g. 5.5-fold reduction) in removing lysosomal contamination. The rate of peroxisomal beta-oxidation with lauroyl-CoA (C12:0) as substrate was the highest of all fatty acyl-CoAs tested. Butyryl-CoA (C4:0) was not oxidized by purified peroxisomes. In general, as chain length of the fatty acyl-CoAs increased above 12 carbons, the rates of beta-oxidation decreased.

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