首页> 外文期刊>Plant and cell physiology >Asparagine Synthetase1, but not Asparagine Synthetase2, is Responsible for the Biosynthesis of Asparagine Following the Supply of Ammonium to Rice Roots
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Asparagine Synthetase1, but not Asparagine Synthetase2, is Responsible for the Biosynthesis of Asparagine Following the Supply of Ammonium to Rice Roots

机译:天冬酰胺合成酶1,而不是天冬酰胺合成酶2,是负责向水稻根部供应铵后天冬酰胺的生物合成的。

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摘要

Asparagine is synthesized from glutamine by the reaction of asparagine synthetase (AS) and is the major nitrogen form in both xylem and phloem sap in rice (Oryza sativa L.). There are two genes encoding AS, OsAS1 and OsAS2, in rice, but the functions of individual AS isoenzymes are largely unknown. Cell type-and NH4+-inducible expression of OsAS1 as well as analyses of knockout mutants were carried out in this study to characterize AS1. OsAS1 was mainly expressed in the roots, with in situ hybridization showing that the corresponding mRNA was specifically accumulated in the three cell layers of the root surface (epidermis, exodermis and sclerenchyma) in an NH4+-dependent manner. Conversely, OsAS2 mRNA was abundant in leaf blades and sheathes of rice. Although OsAS2 mRNA was detectable in the roots, its content decreased when NH4+ was supplied. Retrotransposon-mediated knockout mutants lacking AS1 showed slight stimulation of shoot length and slight reduction in root length at the seedling stage. On the other hand, the mutation caused an approximately 80-90% reduction in free asparagine content in both roots and xylem sap. These results suggest that AS1 is responsible for the synthesis of asparagine in rice roots following the supply of NH4+. Characteristics of the NH4+-dependent increase and the root surface cell-specific expression of OsAS1 gene are very similar to our previous results on cytosolic glutamine synthetase1;2 and NADH-glutamate synthase1 in rice roots. Thus, AS1 is apparently coupled with the primary assimilation of NH4+ in rice roots.
机译:天冬酰胺是由谷氨酰胺通过天冬酰胺合成酶(AS)的反应合成的,并且是水稻(Oryza sativa L.)木质部和韧皮部树液中的主要氮形式。水稻中有两个编码AS的基因OsAS1和OsAS2,但是单个AS同工酶的功能很大程度上未知。在这项研究中进行了OsAS1的细胞类型和NH4 +诱导型表达以及敲除突变体的分析,以表征AS1。 OsAS1主要在根中表达,原位杂交表明相应的mRNA以NH4 +依赖的方式特异性地积累在根表面的三个细胞层(表皮,外皮和硬化组织)中。相反,OsAS2 mRNA在水稻叶片和鞘中含量丰富。尽管在根中可检测到OsAS2 mRNA,但是当提供NH4 +时其含量下降。缺少AS1的逆转座子介导的敲除突变体在苗期显示出对芽长的轻微刺激和根长的轻微降低。另一方面,该突变导致根和木质部树液中游离天冬酰胺含量降低约80-90%。这些结果表明,在供应NH4 +后,AS1负责水稻根中天冬酰胺的合成。 OsAS1基因的NH4 +依赖性增加和根表面细胞特异性表达的特征与我们先前对水稻根中胞质谷氨酰胺合成酶1、2和NADH-谷氨酸合成酶1的研究结果非常相似。因此,AS1显然与稻根中NH4 +的主要同化结合。

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