Characterization of novel D-hordeins from Psathyrostachys juncea
Three genes encoding novel D-hordeins, Ns 1.3 , Ns 2.6 , and Ns 2.9 were isolated from Psathyrostachys juncea . The Ns 1.3 differed from Ns 2.6 and Ns 2.9 by having a shorter open reading frame (< 1.5 kb versus > 2.5 kb), and was probably not expressed as a normal protein, while the activities...
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Veröffentlicht in: | Biologia plantarum 2018-06, Vol.62 (2), p.369-378 |
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Sprache: | eng |
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Zusammenfassung: | Three genes encoding novel D-hordeins,
Ns 1.3
,
Ns 2.6
, and
Ns 2.9
were isolated from
Psathyrostachys juncea
. The Ns 1.3 differed from Ns 2.6 and Ns 2.9 by having a shorter open reading frame (< 1.5 kb
versus
> 2.5 kb), and was probably not expressed as a normal protein, while the activities for Ns 2.6 and Ns 2.9 were verified by bacterial expression. Though highly similar primary structure to wheat high molecular mass glutenin subunits (HMM-GSs) and barley D-hordeins, Ns 2.6 and Ns 2.9 had more cysteine residues (nine in total) and a larger molecular mass than HMMGSs, and a longer N-terminal length than D-hordeins. Phylogenetic analysis revealed that the
Ps. juncea
D-hordeins were divided into Ns 1.3 type and Ns 2.6/Ns 2.9 type. Divergence times indicated that
Ns 1.3
diverged the earliest from the orthologous
Triticeae
locus, while
Ns 2.6
and
Ns 2.9
and the D-hordeins from two
Hordeum
species diverged nearly at the same time from those loci, and the divergence between the D-hordeins of
H. chilense
and
Ns 2.6/Ns 2.9
was more recent than between the two
Hordeum
species. The novel
Ps. juncea
D-hordeins have the potential to be very important for improving the end-use quality of wheat flours because of the presence of extra cysteine residues and longer repetitive domain, in addition they can contribute to the understanding of the evolution of
Triticeae
prolamins. |
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ISSN: | 0006-3134 1573-8264 |
DOI: | 10.1007/s10535-018-0775-6 |