1.1.1.18	1-oxo-D-chiro-inositol + NADH + H+	-	
1.1.1.18	D-2,3-diketo-4-deoxy-epi-inositol + NADH	-	
1.1.1.18	additional information	the enzyme shows a broad substrate spectrum while remaining highly stereoselective. BsIDH is able to oxidize the mono-saccharides alpha-D-glucose and alpha-D-xylose but not beta-D-glucose, D-mannose and D-galactose	
1.1.1.18	myo-inositol + NAD+	-	
1.1.1.18	myo-inositol + NAD+	involved in rhizopine utilization	
1.1.1.18	myo-inositol + NAD+	should be classified as A-type enzyme	
1.1.1.18	myo-inositol + NAD+	involved in nitrogen fixation and nodulation of soybean	
1.1.1.18	myo-inositol + NAD+	75 times lower activity compared to the reverse reaction	
1.1.1.18	myo-inositol + NAD+	first enzyme in the catabolic pathway of myo-inositol	
1.1.1.18	myo-inositol + NAD+	the NAD+-dependent enzyme catalyses the oxidation of the axial hydroxyl group of myo-inositol to form scyllo-inosose	
1.1.1.18	pinitol + NADH + H+	i.e. 3-O-methyl-D-chiro-inositol. Bacillus subtilis can utilize pinitol as the sole carbon source via the same myo-inositol catabolic pathway