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Despite the importance of chemical cues for larval settlement, their actual identities are poorly described, and only very few elicitors have been fully chemically characterized and assigned to a defined natural source [3], [4], [5], [6], [7].
Two isomers of C59N CF3 11 were characterized and assigned to the most stable isomers predicted by DFT.
Proteins found in living organisms have been isolated, characterized, and assigned to different functional classes having related structures and functions.
For the H NMR spectroscopy Borer et al. had previously characterized and assigned the imino proton shifts of a stabilized SL3 derivative (WT-3).
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This system was further exploited to characterize and assign the function of proteins encoded in the biosynthetic gene cluster in the maturation of lichenicidin peptides.
Bacterial phenotypes were characterized and previously assigned to biotypes [ 13, 24].
At necropsy, lesions were characterized and scores assigned for 3 internal tissues, air sacs, pericardium and liver, as described by Peighambari et al. [ 20].
The remaining 6 loci were successfully characterized and sufficient to assign the isolate to cc23.
Although many genes have not been assigned COG functions, many are poorly characterized, and, still, many have been assigned more than one COG function, the COG function data in publicly-available NCBI Protein Table files (.ptt) was used for this analysis.
†The sequence type for 1 clonal complex 23 strain was not available because of failure of existing primers to amplify the glucose-6-phosphate dehydrogenase (gdh) locus, but the remaining 6 loci were successfully characterized and were sufficient to assign the isolate to clonal complex 23.
The major byproduct was isolated, characterized by mass spectrometry, and assigned as desulfurized starting material, namely, 3′-alanylamino-3′-deoxy-RNA.
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