Abstract：
:Escherichia coli KJ122 was engineered to produce succinate from glucose using the wild type GalP for glucose uptake instead of the native phosphotransferase system (ptsI mutation). This strain now ferments 10% xylose poorly. Mutants were selected by serial transfers in AM1 mineral salts medium with 10% xylose. Clones from this population all exhibited a similar improvement, co-fermentation of an equal mixture of xylose and glucose. One of these, AS1600a, produced 84.26 ± 1.37 g/L succinate, equivalent to that produced by the parent (KJ122) from 10% glucose (85.46 ± 1.78 g/L). AS1600a was sequenced and found to contain a mutation in galactose permease (GalP, G236D). This mutation was shown to be responsible for the improvement in fermentation using KJΔgalP as the host and expression vectors with native galP and with mutant galP(∗). Strain AS1600a and KJΔgalP(pLOI5746; galP(∗)) also co-fermented a mixture of glucose, xylose, arabinose, and galactose in sugarcane bagasse hydrolysate using mineral salts medium.
journal_name
Bioresour Technoljournal_title
Bioresource technologyauthors
Sawisit A,Jantama K,Zheng H,Yomano LP,York SW,Shanmugam KT,Ingram LOdoi
10.1016/j.biortech.2015.06.108subject
Has Abstractpub_date
2015-10-01 00:00:00pages
433-41eissn
0960-8524issn
1873-2976pii
S0960-8524(15)00899-8journal_volume
193pub_type
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