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Differential Substrate Inhibition Couples Kinetically Distinct 4-Coumarate:Coenzyme a Ligases With Spatially Distinct Metabolic Roles in Quaking Aspen

机译:差异底物抑制耦合动力学上不同的4-香豆酸酯:辅酶a具有空间不同代谢作用的白杨在颤抖白杨。

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摘要

4-Coumarate:coenzyme A ligase (4CL) activates hydroxycinnamates for entry into phenylpropanoid branchways that support various metabolic activities, including lignification and flavonoid biosynthesis. However, it is not clear whether and how 4CL proteins with their broad substrate specificities fulfill the specific hydroxycinnamate requirements of the branchways they supply. Two tissue-specific 4CLs, Pt4CL1 and Pt4CL2, have previously been cloned from quaking aspen (Populus tremuloides Michx.), but whether they are catalytically adapted for the distinctive metabolic roles they are thought to support is not apparent from published biochemical data. Therefore, single- and mixed-substrate assays were conducted to determine whether the 4CLs from aspen exhibit clear catalytic identities under certain metabolic circumstances. Recombinant Pt4CL1 and Pt4CL2 exhibited the expected preference forp-coumarate in single-substrate assays, but strong competitive inhibition favored utilization of caffeate andp-coumarate, respectively, in mixed-substrate assays. The Pt4CL1 product, caffeoyl-CoA, predominated in mixed-substrate assays with xylem extract, and this was consistent with the near absence of Pt4CL2 expression in xylem tissue as determined by in situ hybridization. It is interesting that the Pt4CL2 product p-coumaroyl-CoA predominated in assays with developing leaf extract, although in situ hybridization revealed that both genes were coexpressed. The xylem extract and recombinant 4CL1 data allow us to advance a mechanism by which 4CL1 can selectively utilize caffeate for the support of monolignol biosynthesis in maturing xylem and phloem fibers. Loblolly pine (Pinus taeda), in contrast, possesses a single 4CL protein exhibiting broad substrate specificity in mixed-substrate assays. We discuss these 4CL differences in terms of the contrasts in lignification between angiosperm trees and their gymnosperm progenitors.
机译:4-香豆酸酯:辅酶A连接酶(4CL)激活羟基肉桂酸酯,以进入支持各种代谢活动(包括木质化和类黄酮生物合成)的苯丙烷分支。但是,尚不清楚具有广泛底物特异性的4CL蛋白是否以及如何满足它们提供的分支的特定羟基肉桂酸酯要求。先前已从地震白杨(Populus tremuloides Michx。)克隆了两个组织特异性4CL,即Pt4CL1和Pt4CL2,但是从已发表的生化数据来看,它们是否催化适应了它们所支持的独特代谢作用。因此,进行了单底物和混合底物测定,以确定在某些代谢情况下,来自白杨的4CL是否显示出清晰的催化特性。重组Pt4CL1和Pt4CL2在单底物测定中显示出对香豆酸的预期偏爱,但强烈的竞争抑制作用分别在混合底物测定中有利于咖啡因和对香豆酸的利用。 Pt4CL1产物咖啡酰辅酶A在木质部提取物的混合底物检测中占主导地位,这与木质部组织中原位杂交确定的Pt4CL2表达几乎不存在是一致的。有趣的是,Pt4CL2产物p-香豆酰辅酶A在发育中的叶提取物中的测定中占主导地位,尽管原位杂交显示这两个基因是共表达的。木质部提取物和重组4CL1数据使我们能够发展一种机制,通过该机制,4CL1可以选择性地利用咖啡因来支持木质素和韧皮部纤维成熟中的单木酚生物合成。相比之下,火炬松(Pinus taeda)具有单一4CL蛋白,在混合底物测定中表现出广泛的底物特异性。我们根据被子植物树和裸子植物祖细胞木质化的差异来讨论这些4CL差异。

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