Cloning and functional analysis of soluble acid invertase 2 gene (SbSAI-2) in sorghum

文献类型： 外文期刊

第一作者： Wuyuntanmanda

作者： Wuyuntanmanda;Han, Fen-Xia;Dun, Bao-Qing;Zhang, Ji;Wang, Zhi;Sui, Yi;Li, Gui-Ying;Zhu, Li

作者机构：

关键词： Composition and content of sugar; Invertase activity; Sorghum SbSAI-2; Sucrose metabolism

期刊名称：PLANTA （ 影响因子：4.54； 五年影响因子：4.689 ）

ISSN： 0032-0935

年卷期： 2022 年 255 卷 1 期

页码：

收录情况： SCI

摘要： Main conclusion The sorghum soluble acid invertase gene SbSAI-2 was cloned and the function verified in Pichia pastoris and rice, showing the SbSAI-2 affects composition and content of sugar in stem juice. Sugar metabolism is one of the most important metabolic processes in plants, in which soluble acid invertase plays a key role. However, the structure and function of the soluble acid transferase gene in sorghum are still fully unclear. In this study, SbSAI-2 was cloned from the sorghum variety BTx623, and two transcripts were found through sequence analysis, with only one transcript translated into an active protein. There is 72% homology between SbSAI-2 and OsVIN2. The construction of Osvin2 mutant lines and SbSAI-2-1 overexpression lines in Oryza sativa L. japonica. cv. Nipponbare were produced to clarify the invertase functionality. While the invertase activity in the stem of the Osvin2 mutant line was reduced, with no significant difference (P > 0.05), and the contents of fructose and glucose in stem tissue did not change significantly (P > 0.05), and the content of sucrose increased by 38.89% (P < 0.01). In SbSAI-2-1 overexpression lines, the invertase activity in stem was increased by more than 20 times (P < 0.01). The contents of glucose and fructose in stem tissues were increased by two and three times, respectively (P < 0.01), while the content of sucrose was significantly decreased, which was below the detection limit (P < 0.01). This study indicated that SbSAI-2 is a key enzyme related to sucrose metabolism and affects the composition and content of sugar in stems. The result provided further the gene function verification and laid a foundation for the development of molecular markers.

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