Description
NRPS-independent siderophore synthetase that catalyzes the rhizoferrin biosynthesis from citrate and diaminobutane via an ATP-dependent condensation of citrate with diaminobutane followed by the addition of a second citrate to the monocitryl-diaminobutane intermediate (PubMed:28610916). Can also use as substrates the citrate and diaminobutane homologs oxaloacetic acid, diaminopropane, diaminobutane, diaminopentane, tricarballylic acid, hydroxylamine and ornithine (PubMed:28610916). Forms only a mono-substituted intermediate with oxaloacetic acid and diaminopentane whereas both mono-citryl intermediates and full rhizoferrin derivatives were detected when diaminopropane, and ornithine were used as substrates (PubMed:28610916). Tricarballylic acid only forms a rhizoferrin derivative, but no mono-substituted intermediate (PubMed:28610916).
Species
Rhizopus delemar (strain RA 99-880 / ATCC MYA-4621 / FGSC 9543 / NRRL 43880)
Sequence
MPVASSEYQNEHYASFATTSRLVTCLVSETLVPVFFVPVKSVDRNNQFIGLCLLLRPTTVKQESELPTNITASDILTVVPLRGLPILNNERVALFNGIRCPQIDLVDFLDMLPHIYSVESSGSLKSGDSLKQKTFDTLSAILDGNKTFDLVDGYSAVQLWNHFAQDLEINSKLREQIGQELGSSILFQKYTYDNPKPLPTLNSSTIKWEQSVVEGHATHPMHKARKSFPPMPPLNPGSYDLDHPAVRLVGIPRENAILRGEYEELSAPLVNALMDAGGNHKDIRAQYQNYVFIAIHELQLPNIQEKFKDAVIFSKEHQLNVEALASLRSVARPDILPGLSVKLCLGIKISSALRTVTPFTTYFGPGFSFNVVPKLTYDHEVLAIERELGTITYRHEDSDVAKHCSSVIREALEYDPKYQDDLFIPCGALVEKIQRPDTDETLVAHVWNLDTKEKRVEFLDRYVDFALRSFLPPCLINGVAFEAHGQNTLARFDRKTGLLKGFVIRDFGGVKAHNETLKKSAGVELDILPDSCVEAHSLEEVFKLLYHTLFHCQLQRLIRVLDLHYSGEGWEIVRKYLTQYVPKDHVMWPMFMESSKVPGKCLVRMKIDELYRDYIYRPVPNMIKYEPQSVPEAI
Simulated SDS-PAGE

(Note: Representative image - actual molecular weight may vary depending on tag type and expression method)
Safety
Upon ordering, we will perform rigorous biosecurity and export control screening to ensure that order fulfillment is consistent with all legal and regulatory guidance.
Protein synthesis service