Kumar S
J Biol Chem. 1975 Jul 10;250(13):5150-8.
Fatty acid synthetase complex (Mr = 500,000) purified from pigeon liver homogenates is inactivated by phenylmethylsulfonyl fluoride. A well characterized inhibitor of serine esterases. Pseudounimolecular kinetics are followed at all inhibitor concentrations studied (0.05 to 1.0 mM). The second order rate constant obtained at pH 7.0, 30 degrees in 0.05 M potassium phosphate, 1 mM EDTA is 250 plus or minus 10 M-1 min-1 and appears to be independent of pH between 6 and 7.9. The inactivation of the enzyme complex appears to be selective since only one of the several component enzymes of fatty acid synthesis, palmityl-CoA deacylase, is inhibited. Acetyl- and malonyl-CoA-pantetheine transacylase activities as well as the kinetics of the reduction and dehydration steps are nearly identical for the native and the modified enzymes. The rate of approach of the condensation-CO2 exchange reaction (substrates: hexanoyl-CoA, malonyl-CoA, CoA, and H14CO3-) is slightly slower in the modified enzyme, though this change is not large enough to account for total loss of activity for fatty acid synthesis. The rate of loss of palmityl-CoA deacylase activity at a constant inhibitor concentration follows biphasic kinetics. Complete inactivation is achieved only after 2 mol of the inhibitor are bound per mol of the enzyme complex. Acetyl-, butyryl-, and hexanoyl-CoA thioesters (at 1.0 mM concentrations) protect the enzyme complex against inactivation by phenylmethylsulfonyl fluoride whereas CoA has no effect. Malonyl-CoA on the other hand, promotes inhibitor-mediated inactivation. Of the N-acetyl cysteamine derivatives tested, S-acetyl-N-acetyl cysteamine (at 10 mM) gives almost complete protection against inactivation whereas S-acetoacetyl-, S-beta-hydroxybutyryl-, and S-crotonyl-N-acetyl cysteamine thioesters exhibit either slight or no protection. These data demonstrate that phenylmethylsulfonyl fluoride is a selective reagent for the inactivation of functional fatty acyl deacylase component(s) of the pigeon liver fatty acid synthetase complex, and that it has no effect on malonyl or acetyl transacylases. The data are also in accord with the postulation that the inhibitor interacts at two catalytic centers of the enzyme complex. Furthermore, the patterns of protective effects shown by saturated acyl-CoA asters and malonyl-CoA point to different mechanisms of deacylation for these esters.
从鸽肝匀浆中纯化得到的脂肪酸合成酶复合物(分子量 = 500,000)可被苯甲基磺酰氟失活,苯甲基磺酰氟是一种特性明确的丝氨酸酯酶抑制剂。在所有研究的抑制剂浓度(0.05至1.0 mM)下均呈现假一级动力学。在pH 7.0、30℃、0.05 M磷酸钾、1 mM乙二胺四乙酸(EDTA)条件下获得的二级速率常数为250 ± 10 M⁻¹ min⁻¹,并且在pH 6至7.9之间似乎与pH无关。该酶复合物的失活似乎具有选择性,因为脂肪酸合成的几种组成酶中只有一种,即棕榈酰辅酶A脱酰酶受到抑制。天然酶和修饰酶的乙酰辅酶A和丙二酰辅酶A - 泛酰巯基乙胺转酰基酶活性以及还原和脱水步骤的动力学几乎相同。修饰酶中缩合 - CO₂交换反应(底物:己酰辅酶A、丙二酰辅酶A、辅酶A和H¹⁴CO₃⁻)的反应速率略慢,尽管这种变化不足以解释脂肪酸合成活性的完全丧失。在恒定抑制剂浓度下,棕榈酰辅酶A脱酰酶活性的丧失速率遵循双相动力学。只有在每摩尔酶复合物结合2摩尔抑制剂后才能实现完全失活。乙酰辅酶A、丁酰辅酶A和己酰辅酶A硫酯(浓度为1.0 mM)可保护酶复合物免受苯甲基磺酰氟的失活作用,而辅酶A则无此作用。另一方面,丙二酰辅酶A会促进抑制剂介导的失活。在所测试的N - 乙酰半胱胺衍生物中,S - 乙酰 - N - 乙酰半胱胺(浓度为10 mM)几乎能完全保护酶复合物免失活,而S - 乙酰乙酰 - 、S - β - 羟基丁酰 - 和S - 巴豆酰 - N - 乙酰半胱胺硫酯要么只有轻微保护作用,要么没有保护作用。这些数据表明,苯甲基磺酰氟是使鸽肝脂肪酸合成酶复合物的功能性脂肪酰脱酰酶成分失活的选择性试剂,并且它对丙二酰或乙酰转酰基酶没有影响。这些数据也符合抑制剂在酶复合物的两个催化中心相互作用的推测。此外,饱和酰基辅酶A酯和丙二酰辅酶A所显示的保护作用模式表明这些酯的脱酰基机制不同。