Borate also inhibited nicotinamide adenine dinucleotide (NAD) (Roush and Norris 1950; Strittmatter 1964; Deitrich 1967; Deal 1969). Moreover, it is known that the hydroxyl groups of NAD forms complexes with the borate compound (Johnson and Smith 1976). Boron having adjacent hydroxyl groups (transferases) has a tendency to form complexes with organic molecules. It may have an interaction with important biological substances, containing polysaccharides, pyridoxine, riboflavin, dehydroascorbic acid, and the pyridine nucleotides. (Samman et al. 1998; Deviran and Volpe 2003) It binds strongly to furanoid cis-diols, which include erythritan, ribose, and apiose; apiose is present throughout the cell walls of vascularplants (Loomis and Durst 1992; Hunt 2012).Nicotinamide adenine dinucleotide (NAD+) and nicotinamide adenine dinucleotide phosphate (NADP) contain ribose components that are active in energy metabolism; binding to them affects certain metabolic pathway processes (Hunt 2012). Hunt (2012) reported that NAD+ is an essential cofactor for five sub-sub-classes of oxidoreductase enzymes and has a strong relevance for boron. The diadenosine-phosphates (ApnA) are structurally similar to NAD+. Compared to NAD+, boron binding by Ap4A, Ap5A, and Ap6A is greatly enhanced; however, the binding is still less than that to S-adenosylmethionine (SAM).
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