二萜合成酶中的重要残基对水稻植物鞘氨醇 A-F 的生物合成至关重要。

Takumi Miwa, Oto Ishikawa, Yuri Takeda-Kimura, Tomonobu Toyomasu
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引用次数: 0

摘要

栽培稻(Oryza sativa)能产生多种二萜类植物雌酚。在 O. sativa cv. Nipponbare 中发现了负责生物合成莫米内酯、植物黄烷和oryzalexins 的二萜合成酶基因。OsKSL10 (在 RAP 中为 Os12t0491800,在 MSU 中为 LOC_Os12g30824)先前被鉴定为催化ent-copalyl diphosphate 向 ent-sandaracopimaradiene 转化的酶,用于生产 oryzalexins A 至 F。我们之前对亚洲栽培稻的野生祖先 Oryza rufipogon 的研究表明,OrKSL10 和 OrKSL10ind 分别来自 O. rufipogon 的 W1943 和 W0106(与粳亚种和籼亚种亲缘关系密切),可将二磷酸ent-copalyl 转化为 ent-miltiradiene。因此,ent-miltiradiene 合酶向 ent-sandaracopimaradiene 合酶的功能转化可能是通过天然氨基酸突变实现的,其细节尚未阐明。在本研究中,我们发现在 OrKSL10 中引入 A654G 取代后,其功能发生了显著变化,变得更接近 OsKSL10。此外,V546I/A654G双取代几乎完全将OrKSL10的功能转化为OsKSL10的功能。另一方面,反向置换 I546V/G654A 不足以将 OsKSL10 的功能转化为 OrKSL10,这表明 OsKSL10 的功能需要引入额外的置换 S522I。最后,OrKSL10 中 654A 残基上的点突变表明,该位置上的疏水侧链对ent-sandaracopimaradiene 的产生有负面影响。
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Essential residues in diterpene synthases for biosynthesis of oryzalexins A-F in rice phytoalexin

Cultivated rice (Oryza sativa) produces a variety of diterpenoid-type phytoalexins. Diterpene synthase genes that are responsible for the biosynthesis of momilactones, phytocassanes, and oryzalexins have been identified in O. sativa cv. Nipponbare. OsKSL10 (Os12t0491800 in RAP and LOC_Os12g30824 in MSU) was previously identified as an enzyme catalyzing the conversion of ent-copalyl diphosphate to ent-sandaracopimaradiene for the production of oryzalexins A to F. Our previous study on Oryza rufipogon, a wild progenitor of Asian cultivated rice, showed that both OrKSL10 and OrKSL10ind from O. rufipogon accessions W1943 and W0106, respectively, closely related to the japonica and indica subspecies, converted ent-copalyl diphosphate to ent-miltiradiene. Thus, the functional conversion of ent-miltiradiene synthase into ent-sandaracopimaradiene synthase is implied to have occurred through natural amino acid mutations, the details of which have not been elucidated. In this study, we show that introduction of A654G substitution into OrKSL10 significantly alters its function into more closely resembling that of OsKSL10. Moreover, double substitution V546I/A654G almost completely converts the function of OrKSL10 into that of OsKSL10. On the other hand, the reversed substitution I546V/G654A was insufficient to convert the function of OsKSL10 into OrKSL10, indicating the introduction of additional substitution S522I is required for the functionality of OsKSL10. Lastly, point mutations at the 654A residue in OrKSL10 suggest that hydrophobic side chains at this position have a negative influence on the production of ent-sandaracopimaradiene.

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