Abstract
D-Xylonic acid is one of the top 30 most desirable chemicals to be derived from biomass sugars identified by the US Department of Energy, being applicable as a non-food substitute for D-gluconic acid and as a platform chemical. We engineered the non-conventional yeast Pichia kudriavzevii VTT C-79090T to express a D-xylose dehydrogenase coding gene from Caulobacter crescentus. With this single modification the recombinant P. kudriavzevii strain produced up to 171g L-1 of D-xylonate from 171g L-1 d-xylose at a rate of 1.4g L-1h-1 and yield of 1.0g [g substrate consumed]-1, which was comparable with D-xylonate production by Gluconobacter oxydans or Pseudomonas sp. The productivity of the strain was also remarkable at low pH, producing 146g L-1 D-xylonate at 1.2g L-1h-1 at pH 3.0. This is the best low pH production reported for D-xylonate. These results encourage further development towards industrial scale production.
| Original language | English |
|---|---|
| Pages (from-to) | 555-562 |
| Journal | Bioresource Technology |
| Volume | 133 |
| DOIs | |
| Publication status | Published - 1 Jan 2013 |
| MoE publication type | A1 Journal article-refereed |
Funding
This work has been financially supported by the Academy of Finland through the Centre of Excellence in White Biotechnology – Green Chemistry (Grant 118573 ) and the European Commission through the Seventh Framework Programme (FP7/2007-2013) under Grant agreement N° FP7-241566 BIOCORE. Financial support from the VTT Graduate School is acknowledged (Yvonne Nygård).
Keywords
- D-Xylonate
- D-Xylose
- Issatchenkia orientalis
- Low pH
- Pichia kudriavzevii