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A yield of fine fiber from the retted stems processed through the Flax-PP was acquired from further cleaning and refining by passage through a Shirley Analyzer.
Only a small proportion of the TEs described in the flax genome could be identified through alignment to previously characterized elements from other species [ 40].
Using the same approach for gene discovery, we compared the size of the flax BGAL families in 23 representative plant genomes obtained through Phytozome (version 8.0) [ 14].
The morphology of the flax oil microcapsules depended on the zein:flax oil ratio and the process used for microencapsulation.
Linola flax seeds (control) were obtained from the Flax and Hemp Collection of the Institute of Natural Fibres, Poland.
Flax seeds (cv. Linola) were obtained from The Flax and Hemp Collection of the Institute of Natural Fibres, Poland.
Further genetic analysis is needed on the flax plants to identify CAD isoforms in flax, as well as other research to confirm SAD enzyme activity in flax.
Following the release of the flax draft genome, a flax UGT (GeneBank accession # JN088324.1) was reported [ 27].
Microarray data corresponding to the flax BGALs were then extracted.
Flax seeds (Linum usitatissimum L., fibrous cultivar Nike) were obtained from the flax and hemp collection of the Institute of Natural Fibres of Poland.
Comparison of the flax UGTs with orthologs from four other sequenced dicot genomes indicated that seven UGTs were flax diverged.
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