Alpha-mannosidosis (AM; OMIM 248500) is a rare autosomal recessive lysosomal storage disorder caused by mutations in , which codes for the lysosomal alpha-mannosidase enzyme (LAMAN; EC:3.2.1.
View Article and Find Full Text PDFTo manage stem canker disease on royal poinciana, actinobacterial isolates were used as biological control agents (BCAs) based on their strong inhibitory effects against . UAE2 and UAE1 had the ability to produce antifungal compounds and cell-wall-degrading enzymes (CWDEs). Only , however, restored the activity of 1-aminocyclopropane-1-carboxylate (ACC) deaminase (ACCD).
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