6 results match your criteria: "Horticultural and Food Research Institute of New Zealand Ltd.[Affiliation]"
J Clin Lab Anal
January 2009
Functional Foods and Health Programme, The Horticultural and Food Research Institute of New Zealand Ltd., Auckland, New Zealand.
Introduction: Point-of-care (POC) measurements using saliva samples have immense potential to assess systemic health and wellbeing, but sample viscosity and contaminants can affect analyses. We sought a portable clean-up method for whole saliva appropriate for use with POC measurement techniques such as biosensors.
Methods: Whole saliva from each of 13 male subjects was split into 5 fractions.
Phytochemistry
July 2007
The Horticultural and Food Research Institute of New Zealand Ltd., Private Bag 11030, Palmerston North 4442, New Zealand.
Biosynthesis of lilac compounds in 'Hortgem Tahi' kiwifruit (Actinidia arguta) flowers was investigated by treating inflorescences with d(5)-linalool. The incorporation of the deuterium label into 8-hydroxylinalool, 8-oxolinalool, the lilac aldehydes, alcohols, and alcohol epoxides was followed by GC-MS and enantioselective GC-MS. Both (R)- and (S)-linalool were produced naturally by the flowers, but 8-hydroxylinalool, 8-oxolinalool, and the lilac aldehydes and alcohols occurred predominantly as the (S) and 5'(S)-diastereoisomers, respectively.
View Article and Find Full Text PDFPhytochemistry
April 2006
The Horticultural and Food Research Institute of New Zealand Ltd., Department of Industrial Biotechnology, Palmerston North.
Lilac alcohol epoxide (2-(5-methyl-5-(oxiran-2-yl)-tetrahydrofuran-2-yl)propan-1-ol), a previously unreported monoterpene, was identified in the solvent extract of the flowers of seven Actinidia arguta genotypes. The diastereomeric lilac alcohol epoxides co-occurred with the lilac aldehydes and alcohols. Another compound, the lilac diol (2-(5-(1-hydroxyethyl)-5-methyl-tetrahydrofuran-2-yl)propan-1-ol) was synthesised as part of our efforts to identify the lilac alcohol epoxide.
View Article and Find Full Text PDFFEBS J
June 2005
Molecular Olfaction Group, Mt Albert Research Centre, The Horticultural and Food Research Institute of New Zealand Ltd. (HortResearch), Auckland, New Zealand.
Apple flavor is characterized by combinations of ester compounds, which increase markedly during fruit ripening. The final step in ester biosynthesis is catalyzed by alcohol acyl transferases (AATs) that use coenzyme A (CoA) donors together with alcohol acceptors as substrates. The gene MpAAT1, which produces a predicted protein containing features of other plant acyl transferases, was isolated from Malus pumila (cv.
View Article and Find Full Text PDFPhytochemistry
June 2003
The Horticultural and Food Research Institute of New Zealand Ltd, Private Bag 11030, Palmerston North, New Zealand.
More than 240 compounds were detected when the volatile components of the flowers and the fruit from several Actinidia arguta genotypes were investigated. Around 60-70 different compounds were extracted from individual tissues of each genotype. Two different methods of volatile sampling (headspace and solvent) favoured different classes of compounds, dependent upon their volatilities and solubilities in the flower or fruit matrices.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
October 1994
Molecular Genetics Group, Horticultural and Food Research Institute of New Zealand Ltd., Auckland.
White clover mosaic virus strain O (WClMV-O), species of the Potexvirus genus, contains a set of three partially overlapping genes (the triple gene block) that encodes nonvirion proteins of 26 kDa, 13 kDa, and 7 kDa. These proteins are necessary for cell-to-cell movement in plants but not for replication. The WClMV-O 13-kDa gene was mutated (to 13*) in a region of the gene that is conserved in all viruses known to possess triple-gene-block proteins.
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