LaBadie J, Dunn W A, Aronson N N
Biochem J. 1976 Oct 15;160(1):85-95. doi: 10.1042/bj1600085.
The biosynthesis of carnitine in the rat was studied by following the metabolism of two radioactive derivatives of asialo-fetuin. The first contained 14C-labelled methyl groups covalently bound to the 6-N-amino fraction of its lysine residues as 6-N-monomethyl- and dimethyl-lysine. By treating this protein with iodomethane, a second derivative was produced in which the radioactivity was preferentially incorporated as 6-N-[Me-14C]-trimethyl-lysine. These desialylated glycoproteins, like other asialo-proteins, were immediately cleared from the blood by rat liver. Within hepatocyte lysosomes, the 14C-labelled proteins were rapidly hydrolysed, producing free amino acids containing the various 6-N-[Me-14C]methylated lysine residues. The radioactive amino acids crossed the lysosomal membrane and were further metabolized in the cytosol. Carnitine was the major radioactive metabolite detected in extracts of the rat carcass and liver after intravenous injection of 6-N-[Me-14C]trimethyl-lysine-labelled asialo-fetuin. Within 3h, at least 34.6% of the trimethyl-lysine in the administered protein was converted into carnitine. Similarly, an isolated perfused rat liver converted 30% of the added peptide-bound trimethyl-lysine into carnitine within 90 min. On the other hand, in numerous attempts we failed to detect radioactive carnitine in both rat liver and carcass between 20 min and 22 h after injection of 6-N-[Me-14C]-monomethyl- and -dimethyl-lysine-labelled asialo-fetuin. These data provide evidence for a pathway of carnitine biosynthesis that involves trimethyl-lysine as a peptide-bound precursor as proposed by R.A. Cox & C.L. Hoppel [(1973) Biochem. J. 136, 1083-1090] and V. Tanphaichitr & H.P. Broquist [(1973) J. Biol. Chem. 248, 2176-2181]. The findings also show that rat liver can synthesize carnitine without the aid of other tissues, but cannot convert free partially methylated lysines into trimethyl-lysine.
通过追踪去唾液酸胎球蛋白的两种放射性衍生物的代谢情况,对大鼠体内肉碱的生物合成进行了研究。第一种衍生物含有与赖氨酸残基的6-N-氨基部分共价结合的14C标记甲基,分别为6-N-单甲基赖氨酸和二甲基赖氨酸。通过用碘甲烷处理这种蛋白质,产生了第二种衍生物,其中放射性优先以6-N-[甲基-14C]-三甲基赖氨酸的形式掺入。这些去唾液酸化糖蛋白与其他去唾液酸蛋白一样,被大鼠肝脏迅速从血液中清除。在肝细胞溶酶体内,14C标记的蛋白质迅速水解,产生含有各种6-N-[甲基-14C]甲基化赖氨酸残基的游离氨基酸。放射性氨基酸穿过溶酶体膜并在细胞质中进一步代谢。静脉注射6-N-[甲基-14C]三甲基赖氨酸标记的去唾液酸胎球蛋白后,肉碱是在大鼠尸体和肝脏提取物中检测到的主要放射性代谢产物。在3小时内,给药蛋白质中至少34.6%的三甲基赖氨酸转化为肉碱。同样,一个离体灌注的大鼠肝脏在90分钟内将添加的肽结合三甲基赖氨酸的30%转化为肉碱。另一方面,在多次尝试中,我们未能在注射6-N-[甲基-14C]-单甲基赖氨酸和二甲基赖氨酸标记的去唾液酸胎球蛋白后20分钟至22小时之间在大鼠肝脏和尸体中检测到放射性肉碱。这些数据为肉碱生物合成途径提供了证据,该途径涉及三甲基赖氨酸作为肽结合前体,正如R.A.考克斯和C.L.霍佩尔[(197