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Partial cDNAs of AsGGT1 and AsGGT2 were amplified by PCR using Ex Taq DNA polymerase (Takara, Tokyo, Japan) and oligonucleotide primers designed from the nucleotide sequences of two garlic EST clones, i.e., EPP005LLAA12S004013 and EPP005LLAA12S003688 in GarlicESTdb (Kim et al., 2009 1 ): AsGGT1-Core-F (5-ATCGCCACTTCATATGAACC-3) and AsGGT1-Core-R (5-GATAATGCTAGATATGGCTC-3) for AsGGT1

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