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Use of sol-gel entrapment techniques for the resolution of itaconic acid biosynthetic pathway inAspergillus terreus

✍ Scribed by Eyal Bressler; Sergei Braun


Publisher
Springer
Year
1996
Tongue
English
Weight
639 KB
Volume
7
Category
Article
ISSN
0928-0707

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✦ Synopsis


A new technique of investigation of labile metabolic pathways using immobilization of the pathway in sol-gel derived silicate matrices was demonstrated. The biosynthetic pathway of itaconic acid in AspergiZlus terreus is believed to proceed through decarboxylation of cis-aconitate catalyzed by an unstable enzyme aconitate decarboxylase, E.C. 4. I. 1.6. Stabilization of this pathway in sol-gel derived silicate matrix enabled the elucidation of the correct sequence of biosynthetic steps. The decarboxylation of cis-aconitate does not lead directly to itaconate, but rather to citraconate. The latter is then isomerized to itaconate by a previously unknown enzyme.


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✍ Faina Gelman; David Avnir; Herbert Schumann; Jochanan Blum 📂 Article 📅 1999 🏛 Elsevier Science 🌐 English ⚖ 85 KB

Chiral Ru-BINAP, Rh-DIOP and Rh-BPPM complexes have been physically entrapped in sol-gel matrices. The resulting materials are recyclable leach-proof catalysts for enantioselective hydrogenation of itaconic acid. Chiral methylsuccinic acid of o.p. up to 78% is obtained. The complexes, including the