Title of article :
New acetoin reductases from Bacillus stearothermophilus: meso- and 2R,3R-butanediol as fermentation products
Author/Authors :
Giovannini، نويسنده , , Pier Paolo and Mantovani، نويسنده , , Matteo and Grandini، نويسنده , , Alessandro and Medici، نويسنده , , Alessandro and Pedrini، نويسنده , , Paola، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2011
Pages :
6
From page :
15
To page :
20
Abstract :
The fermentation of sucrose with Bacillus stearothermophilus ATCC 2027 afforded 2R,3R- and meso-2,3-butanediol together with R-acetoin following the bacterial catabolic pathway. This metabolic route was confirmed by the conversion of pyruvate to R-acetoin with the cell free extract of B. stearothermophilus. On the other hand the reduction of 3R-acetoin to 2R,3R- and meso-butanediol with the same cell free extract allowed at least the presence of two NADH-dependent reductases. Together with the S-stereospecific diacetyl reductase (BSDR), purified in a previous work, a new S-stereospecific acetoin reductase (S-ACR) was partially purified and a fraction containing R-stereospecific acetoin reductase (R-ACR) was obtained. On the other hand in B. stearothermophilus fermentation of sucrose the “butanediol cycle” is negligible because the acetylacetoin synthase, responsible of the first step of this cycle, is an inducible enzyme that needs low concentration of sugar and high concentration of acetoin to be expressed.
Keywords :
Bacillus stearothermophilus , Metabolic pathway , Diacetyl reductase , Acetoin reductase , Fermentation
Journal title :
Journal of Molecular Catalysis B Enzymatic
Serial Year :
2011
Journal title :
Journal of Molecular Catalysis B Enzymatic
Record number :
1715013
Link To Document :
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