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Construction of a new plant expression vector and the development of maize germplasm expressing the Aspergillus ficuum phytase gene PhyA2

Peng Jiao; Wen-Ya Yuan; Han-Dan Zhao; Jing Qu; Pi-Wu Wang; Shu-Yan Guan; Yi-Yong Ma
Genetic Resources and Crop Evolution · Vol. 68, Issue 3 · pp. 1103-1115 · 2021

Abstract

Phytases, which belong to a special category of orthophosphoric monoester phosphohydrolases, degrade inositol hexaphosphate to produce lower-grade inositol phosphate derivatives and inorganic phosphate. Thus, phytases may improve phosphorus utilization, eliminate the anti-nutrient properties of phytic acid, and mitigate environmental pollution due to phosphorus contamination. In this study, we constructed a new root-specific expression vector by inserting the Aspergillus ficuum phytase gene PhyA2 into pCAMBIA3301-ZmGLU1P-Nos. The subsequent molecular analysis confirmed that six T 4 generation transgenic plants carried and expressed PhyA2 . A quantitative real-time PCR analysis indicated PhyA2 was highly expressed in the transgenic roots. Additionally, the phytase activity was 10.9-fold higher in the transgenic roots (peak activity of 5.432 U/g) than in the control roots. Moreover, compared with the control rhizosphere, the organic phosphorus content in the rhizosphere of the transgenic plants decreased significantly (by up to 5.21 mg/kg). An agronomic trait analysis indicated that PhyA2 expression can increase maize seed weight by up to 25.8 g. Therefore, the integration of PhyA2 into the maize genome can enhance the ability of maize plants to use the phosphorus compounds in soil, while also improving the plant growth status and increasing the seed yield.

Bibliographic Information

JournalGenetic Resources and Crop Evolution
PublisherSpringer
Publication Date2021-03-01
Publication Year2021
Volume68
Issue3
Pages1103-1115
Document TypeJournal Article
Print ISSN0925-9864
eISSN1573-5109
DOI10.1007/s10722-020-01052-w

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NARA Access Coverage1953-01-01~Current
Journal Homepagehttps://www.springer.com/journal/10722
Publisher PageOpen Publisher Page
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