Identification and expression profiling of a novel Kunitz trypsin inhibitor (KTI) gene from turmeric, Curcuma longa, by real-time quantitative PCR (RT-qPCR)
Kunitz trypsin inhibitor (KTI) is one of the widely studied protease inhibitors (PIs) and has been reported to take part in plant defense mechanism during pathogenesis. Numerous plant-origin recombinant KTIs have been described to exhibit anti-pathogenic properties and were used to fight pathogens i...
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Veröffentlicht in: | Acta physiologiae plantarum 2017, Vol.39 (1), p.1-12, Article 12 |
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Zusammenfassung: | Kunitz trypsin inhibitor (KTI) is one of the widely studied protease inhibitors (PIs) and has been reported to take part in plant defense mechanism during pathogenesis. Numerous plant-origin recombinant KTIs have been described to exhibit anti-pathogenic properties and were used to fight pathogens in the field of pharmacology and agriculture. In this study, a novel Kunitz trypsin inhibitor gene,
ClKTI
, was isolated from a medicinal herb plant, turmeric,
Curcuma longa
. The full-length
ClKTI
gene is 754 bp long (Accession No. KF889322.1 in NCBI database) and it was obtained using 5′/3′ rapid amplification of cDNA ends (RACE) technique.
ClKTI
has an open reading frame of 639 bp length which encodes for 213 amino acids and contains the Kunitz-family motif, (V-X-D-X
2
-G-X
2
-L-X
5
-Y-X-I) and an altered reactive site motif, (G/E-I-S). Sequence similarity search using BLASTX showed that
ClKTI
shared the highest similarity to KTI from
Theobroma cacao
with 58% max identity while conserved domains search resulted in
ClKTI
having specific hits with Kunitz-family soybean trypsin inhibitor (STI). Phylogenetic studies suggested that
ClKTI
is related to
T. cacao
while protein homology modeling analysis indicated that it has 12 β-sheets with three disulfide bridges. Using real-time quantitative PCR, the
ClKTI
gene expression pattern in five different tissues (flower, basal stem, stem, rhizome and root) treated with methyl-jasmonate (MeJA) was studied where MeJA was suggested to regulate expression of PI genes in plants. The results indicated that the expression of
ClKTI
generally increased in the MeJA-treated tissues with the root tissues possessing the highest expression and stem tissues showed the highest expression fold-change. |
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ISSN: | 0137-5881 1861-1664 |
DOI: | 10.1007/s11738-016-2311-7 |