Redox Balanced Co-production of Propanediol and 3-Hydroxypropionic Acid from Glycerol Using Novel Recombinant Klebsiella quasipneumonia MSN12
JOURNAL OF INORGANIC AND ORGANOMETALLIC POLYMERS AND MATERIALS(2023)
摘要
The redox imbalance is the major obstacle in the microbial production of 3-hydroxypropionic acid (3-HP). Co-production of propanediol (PDO) and 3-HP is an effective strategy to overcome the redox imbalance issue. The biocatalyst Klebsiella pneumoniae naturally co-produces PDO and 3-HP. Its poor growth characteristics and excessive production of lipopolysaccharide hurdle its usage in industries. The objective of this study is to circumvent these constraints by isolating a novel strain of K. quasipneumoniae MSN12 ( Kp MSN12) from soil samples. From a numerous isolate, the new isolate Kp MSN12 has produced 58 mM PDO and 4 mM 3-HP, when it was grown in shake flask under microaerobic conditions, which is higher than the control Kp 109. The effect of overexpression of an aldH ( KGSADH ) on co-production of 3-HP and PDO from glycerol was investigated in recombinant Kp MSN12 ( Kp MSN12K). Kp MSN12K produced 45 mM of 3-HP and 30 mM PDO which was observed higher (3-HP 25 mM, PDO 28 mM) than the control strain. While over expressing dhaB in another recombinant ( Kp MSN12D), 3-HP was reduced to 9 mM and 11 mM PDO due to the accumulation of 3-HPA and the growth was severely hampered. In addition, combined overexpression of dhaB and aldH ( Kp MSN12DK) produced 33 mM 3-HP and 25 mM PDO. The lower lipopolysaccharide content in the Kp MSN12 strain was confirmed by comparing 2-keto3-deoxyoctonate content ( Kp MSN12—3.8 µg/mL; Kp 109—5.14 µg/mL). In addition, this new strain exhibited enhanced sedimentation characteristics and higher susceptibility to a variety of antibiotics when compared to Kp 109 strain. These potential characteristics of Kp MSN12 would shape it as a desirable host for the production of industrial chemicals. Graphical Abstract
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关键词
3-hydroxypropionic acid,1,3-Propanediol,Lipopolysaccharides,Glycerol dehydratase,Aldehyde dehydrogenase
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