NodC, a membrane protein that catalyzes the synthesis of the chitin oligosa
ccharide chain, was successfully produced in a soluble form. The truncated
nodC gene encoding only the cytoplasmic domain that deletes the hydrophobic
N-terminus expressed both cytoplasmic and secreted proteins in Drosophila
Schneider 2 cells. The expressed protein maintained the ability to synthesi
ze chitin oligosaccharides, primarily (GlcNAc)(4), similar to the native me
mbrane-bound NodC. This evidence suggests that only the large hydrophilic l
oop of NodC is efficient for enzymatic activity. Moreover, immobilizing the
soluble NodC to a solid phase has no effect on the enzymatic activity. Thi
s, anchoring NodC is not necessary for its activity.