Rates of beta-oxidation of fatty acids of various chain lengths and degrees of unsaturation in highly purified peroxisomes isolated from rat liver

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

Abstract

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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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
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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