Leung Ka-Chun, Li Hong-Ye, Mishra Girish, Chye Mee-Len
Department of Botany, The University of Hong Kong, Pokfulam Road, Hong Kong, China.
Plant Mol Biol. 2004 May;55(2):297-309. doi: 10.1007/s11103-004-0642-z.
In plants, fatty acids synthesized in the chloroplasts are exported as acyl-CoA esters to the endoplasmic reticulum (ER). Cytosolic 10-kDa acyl-CoA-binding proteins (ACBPs), prevalent in eukaryotes, are involved in the storage and intracellular transport of acyl-CoAs. We have previously characterized Arabidopsis thaliana cDNAs encoding membrane-associated ACBPs with ankyrin repeats, designated ACBP1 and ACBP2, which show conservation to cytosolic ACBPs at the acyl-CoA-binding domain. Analysis of the Arabidopsis genome has revealed the presence of three more genes encoding putative proteins with acyl-CoA-binding domains, designated ACBP3, ACBP4 and ACBP5. Homologues of ACBP1 to ACBP5 have not been reported in any other organism. We show by reverse-transcriptase polymerase chain reaction (RT-PCR) analysis that ACBP3 , ACBP4 and ACBP5 are expressed in all plant organs, like ACBP1 and ACBP2 . ACBP4 and ACBP5 that share 81.4 identity and which contain kelch motifs were further investigated. To demonstrate their function in binding acyl-CoA, we have expressed them as (His)6-tagged recombinant proteins in Escherichia coli for in vitro binding assays. Both (His)6-ACBP4 and (His)6-ACBP5 bind [14C]oleoyl-CoA with high affinity, [14C]palmitoyl-CoA with lower affinity and did not bind [14C]arachidonyl-CoA. Eight mutant forms of each protein with single amino acid substitutions within the acyl-CoA-binding domain were produced and analyzed. On binding assays, all mutants were impaired in oleoyl-CoA binding. Hence, these novel ACBPs with kelch motifs have functional acyl-CoA-binding domains that bind oleoyl-CoA. Their predicted cytosol localization suggests that they could maintain an oleoyl-CoA pool in the cytosol or transport oleoyl-CoA from the plastids to the ER in plant lipid metabolism.
在植物中,叶绿体中合成的脂肪酸以酰基辅酶A酯的形式输出到内质网(ER)。胞质中的10 kDa酰基辅酶A结合蛋白(ACBP)在真核生物中普遍存在,参与酰基辅酶A的储存和细胞内运输。我们之前已对拟南芥中编码具有锚蛋白重复序列的膜相关ACBP的cDNA进行了表征,命名为ACBP1和ACBP2,它们在酰基辅酶A结合结构域与胞质ACBP具有保守性。对拟南芥基因组的分析揭示了另外三个编码具有酰基辅酶A结合结构域的假定蛋白的基因,命名为ACBP3、ACBP4和ACBP5。在任何其他生物体中均未报道过ACBP1至ACBP5的同源物。我们通过逆转录酶聚合酶链反应(RT-PCR)分析表明,ACBP3、ACBP4和ACBP5与ACBP1和ACBP2一样,在所有植物器官中均有表达。对具有81.4%同源性且含有kelch基序的ACBP4和ACBP5进行了进一步研究。为了证明它们在结合酰基辅酶A方面的功能,我们已将它们作为带有(His)6标签的重组蛋白在大肠杆菌中表达,用于体外结合测定。(His)6-ACBP4和(His)6-ACBP5都以高亲和力结合[14C]油酰辅酶A,以较低亲和力结合[14C]棕榈酰辅酶A,且不结合[14C]花生四烯酰辅酶A。每种蛋白产生并分析了在酰基辅酶A结合结构域内具有单个氨基酸替换的八种突变形式。在结合测定中,所有突变体在油酰辅酶A结合方面均受损。因此,这些具有kelch基序的新型ACBP具有结合油酰辅酶A的功能性酰基辅酶A结合结构域。它们预测的胞质定位表明,它们可以在植物脂质代谢中维持胞质中的油酰辅酶A库,或将油酰辅酶A从质体运输到内质网。