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Bioconversion of indene to cis (1 S,2 R) indandiol and trans (1 R,2 R) indandiol by Rhodococcus species
cis (1 S,2 R) indandiol or trans (1 R,2 R) indandiol are both potential precursors to (−)- cis (1 S,2 R)-1-aminoindan-2-ol, a key chiral synthon for Crixivan ® (Indinavir), a leading HIV protease inhibitor. Enrichment and isolation studies yielded two Rhodococcus sp. strain B 264-1 (MB 5655) and str...
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Published in: | Journal of fermentation and bioengineering 1998-01, Vol.86 (6), p.550-558 |
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Main Authors: | , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | cis (1
S,2
R) indandiol or
trans (1
R,2
R) indandiol are both potential precursors to (−)-
cis (1
S,2
R)-1-aminoindan-2-ol, a key chiral synthon for Crixivan
® (Indinavir), a leading HIV protease inhibitor. Enrichment and isolation studies yielded two
Rhodococcus sp. strain B 264-1 (MB 5655) and strain I-24 (MA 7205) capable of biotransforming indene to
cis (1
S,2
R) indandiol and
trans (1
R,2
R) indandiol respectively. Isolate MB 5655 was found to have a toluene dioxygenase, while isolate MA 7205 was found to harbor both toluene and naphthalene dioxygenases as well as a naphthalene monooxygenase. When scaled up in a 14-
l bioreactor, MB 5655 produced up to 2.0 g/
l of
cis (1
S,2
R) indandiol with an enantiometric excess greater than 99%. MA 7205 cultivated under similar conditions produced up to 1.4 g/
l of
trans (1
R,2
R) indandiol with an enantiomeric excess greater than 98%. Process development studies yielded titers greater that 4.0 g/
l of
cis indandiol for MB 5655. Due to their resistance to indene toxicity and easy cultivation in bioreactors, both
Rhodococcus sp. strains appeared as good candidates for future strain engineering and process development work. |
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ISSN: | 0922-338X |
DOI: | 10.1016/S0922-338X(99)80005-1 |