4.7 Article

Mutation by DNA shuffling of 5-enolpyruvylshikimate-3-phosphate synthase from Malus domestica for improved glyphosate resistance

Journal

PLANT BIOTECHNOLOGY JOURNAL
Volume 11, Issue 7, Pages 829-838

Publisher

WILEY
DOI: 10.1111/pbi.12074

Keywords

5-enolpyruvylshikimate-3-phosphate synthase; Malus domestica; DNA shuffling; glyphosate tolerance; mutation; transgenic rice

Funding

  1. Key Project Fund of the Shanghai Municipal Committee of Agriculture [2009-6-4, 2011-1-8]
  2. International Scientific and Technological Cooperation [2010DFA62320, 11230705900]
  3. National Natural Science Foundation [31071486]
  4. Key Project Fund of Shanghai Minhang Science and Technology Committee [2012MH059]

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A new 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS) gene from Malus domestica (MdEPSPS) was cloned and characterized by rapid amplification of cDNA ends to identify an EPSPS gene appropriate for the development of transgenic glyphosate-tolerant plants. However, wild-type MdEPSPS is not suitable for the development of transgenic glyphosate-tolerant plants because of its poor glyphosate resistance. Thus, we performed DNA shuffling on MdEPSPS, and one highly glyphosate-resistant mutant with mutations in eight amino acids (N63D, N86S, T101A, A187T, D230G, H317R, Y399R and C413A.) was identified after five rounds of DNA shuffling and screening. Among the eight amino acid substitutions on this mutant, only two residue changes (T101A and A187T) were identified by site-directed mutagenesis as essential and additive in altering glyphosate resistance, which was further confirmed by kinetic analyses. The single-site A187T mutation has also never been previously reported as an important residue for glyphosate resistance. Furthermore, transgenic rice was used to confirm the potential of MdEPSPS mutant in developing glyphosate-resistant crops.

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