Cited by 36Microbial Metabolic Engineering and BioproductionBiofuel production and bioconversionFluid Dynamics and Mixing

Adaptive evolution for fast growth on glucose and the effects on the regulation of glucose transport system in Clostridium tyrobutyricum

Jiang, Ling, Li, Shuang, Hu, Yi, Xu, Qing, Huang, He·2012·Biotechnology and Bioengineering

Abstract

Laboratory adaptive evolution of microorganisms offers the possibility of relating acquired mutations to increased fitness of the organism under the conditions used. By combining a fibrous‐bed bioreactor, we successfully developed a simple and valuable adaptive evolution strategy in repeated‐batch fermentation mode with high initial substrate concentration and evolved Clostridium tyrobutyricum mutant with significantly improved butyric acid volumetric productivity up to 2.25 g/(L h), which is the highest value in batch fermentation reported so far. Further experiments were conducted to pay attention to glucose transport system in consideration of the high glucose consumption rate resulted from evolution. Complete characterization and comparison of the glucose phosphoenolpyruvate (PEP)‐dependent phosphotransferase system (PTS) were carried out in the form of toluene‐treated cells and cell‐free extracts derived from both C. tyrobutyricum wide‐type and mutant, while an alternative glucose transport route that requires glucokinase was confirmed by the phenomena of resistance to the glucose analogue 2‐deoxyglucose and ATP‐dependent glucose phosphorylation. Our results suggest that C. tyrobutyricum mutant is defective in PTS activity and compensates for this defect with enhanced glucokinase activity, resulting in the efficient uptake and consumption of glucose during the whole metabolism. Biotechnol. Bioeng. 2012; 109:708–718. © 2011 Wiley Periodicals, Inc.

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  • Prolonged selection that exceeds the first rapid evolutionary adaptation phase will not necessarily lead to significantly improved phenotypes.

    “For standard ALE in biotechnology this is a critical factor, as prolonged selection that exceeds the first rapid evolutionary adaptation phase will not necessarily lead to significantly improved phenotypes [67];”
  • Growth on lactate leads to altered phenotypes in E. coli, such as decreased acetate overflow in order to tune the cellular energy metabolism.

    “Growth on other carbon sources such as lactate also leads to altered phenotypes, such as decreased acetate overflow in order to tune the cellular energy metabolism [67].”
  • Other studies reported improved growth on many non-evolutionary carbon sources after batch selection with gluconeogenic carbon sources.

    “whereas other studies reported improved growth on many non-evolutionary carbon sources after batch selection with gluconeogenic carbon sources [66,67].”

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References 48 · Cited by 36

Authors
Jiang, L., Li, S., Hu, Y., Xu, Q., & Huang, H.
Affiliations
Nanjing Tech University (CN)
Corresponding author
Huang, He
Venue
Biotechnology and Bioengineering
Publisher
Wiley
Published
2011-12-20
Volume
109
Issue
3
Pages
708-718
ISSN
  • 0006-3592 (ISSN-L)
  • 1097-0290
OpenAlex
W2000558009
Cited by
36
References
48
Citations by year
2026: 1 · 2025: 1 · 2024: 1 · 2023: 1 · 2021: 2 · 2020: 4 · 2019: 4 · 2018: 7 · 2017: 4 · 2016: 1 · 2015: 1 · 2014: 2 · 2013: 6 · 2012: 1
FWCI
1.17
Type
journal article
Language
en
Open access
closed
Locations
  • Biotechnology and Bioengineering (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Microbial Metabolic Engineering and Bioproduction
  • Physical Sciences › Engineering › Biomedical Engineering › Biofuel production and bioconversion
  • Physical Sciences › Engineering › Biomedical Engineering › Fluid Dynamics and Mixing
Keywords
Clostridium tyrobutyricum, adaptive evolution, butyric acid production, glucose transport, phosphoenolpyruvate-dependent phosphotransferase system, glucokinase, 2-deoxyglucose resistance, fibrous-bed bioreactor, repeated batch fermentation, mutant strain
MeSH terms
Adaptation, Biological, Glucose, Gene Expression Regulation, Bacterial, Directed Molecular Evolution, Bioreactors, Butyric Acid, Clostridium tyrobutyricum, Glucose Transport Proteins, Facilitative, Metabolic Networks and Pathways

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