Customized microscale approach for optimizing two-phase bio-oxidations of alkanes with high reproducibility

Abstract Background Numerous challenges remain to achieve industrially competitive space–time yields for bio-oxidations. The ability to rapidly screen bioconversion reactions for characterization and optimization is of major importance in bioprocess development and biocatalyst selection; studies at...

Full description

Bibliographic Details
Main Authors: Johannes F. Kolmar, Oliver Thum, Frank Baganz
Format: Article
Language:English
Published: BMC 2017-10-01
Series:Microbial Cell Factories
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12934-017-0788-4
id doaj-3e700d35614d456f9998251818f90977
record_format Article
spelling doaj-3e700d35614d456f9998251818f909772020-11-24T23:23:52ZengBMCMicrobial Cell Factories1475-28592017-10-0116111110.1186/s12934-017-0788-4Customized microscale approach for optimizing two-phase bio-oxidations of alkanes with high reproducibilityJohannes F. Kolmar0Oliver Thum1Frank Baganz2Advanced Centre for Biochemical Engineering, Department of Biochemical Engineering, University College LondonEvonik Creavis GmbHAdvanced Centre for Biochemical Engineering, Department of Biochemical Engineering, University College LondonAbstract Background Numerous challenges remain to achieve industrially competitive space–time yields for bio-oxidations. The ability to rapidly screen bioconversion reactions for characterization and optimization is of major importance in bioprocess development and biocatalyst selection; studies at conventional lab scale are time consuming and labor intensive with low experimental throughput. The direct ω-oxyfunctionalization of aliphatic alkanes in a regio- and chemoselective manner is efficiently catalyzed by monooxygenases such as the AlkBGT enzyme complex from Pseudomonas putida under mild conditions. However, the adoption of microscale tools for these highly volatile substrates has been hindered by excessive evaporation and material incompatibility. Results This study developed and validated a robust high-throughput microwell platform for whole-cell two-liquid phase bio-oxidations of highly volatile n-alkanes. Using microwell plates machined from polytetrafluoroethylene and a sealing clamp, highly reproducible results were achieved with no significant variability such as edge effects determined. A design of experiment approach using a response surface methodology was adopted to systematically characterize the system and identify non-limiting conditions for a whole cell bioconversion of dodecane. Using resting E. coli cells to control cell concentration and reducing the fill volume it is possible to operate in non-limiting conditions with respect to oxygen and glucose whilst achieving relevant total product yields (combining 1-dodecanol, dodecanal and dodecanoic acid) of up to 1.5 mmol g DCW −1 . Conclusions Overall, the developed microwell plate greatly improves experimental throughput, accelerating the screening procedures specifically for biocatalytic processes in non-conventional media. Its simplicity, robustness and standardization ensure high reliability of results.http://link.springer.com/article/10.1186/s12934-017-0788-4Scale-downC–H activationWhole-cell biocatalysisTwo-liquid phaseMonooxygenaseReproducibility
collection DOAJ
language English
format Article
sources DOAJ
author Johannes F. Kolmar
Oliver Thum
Frank Baganz
spellingShingle Johannes F. Kolmar
Oliver Thum
Frank Baganz
Customized microscale approach for optimizing two-phase bio-oxidations of alkanes with high reproducibility
Microbial Cell Factories
Scale-down
C–H activation
Whole-cell biocatalysis
Two-liquid phase
Monooxygenase
Reproducibility
author_facet Johannes F. Kolmar
Oliver Thum
Frank Baganz
author_sort Johannes F. Kolmar
title Customized microscale approach for optimizing two-phase bio-oxidations of alkanes with high reproducibility
title_short Customized microscale approach for optimizing two-phase bio-oxidations of alkanes with high reproducibility
title_full Customized microscale approach for optimizing two-phase bio-oxidations of alkanes with high reproducibility
title_fullStr Customized microscale approach for optimizing two-phase bio-oxidations of alkanes with high reproducibility
title_full_unstemmed Customized microscale approach for optimizing two-phase bio-oxidations of alkanes with high reproducibility
title_sort customized microscale approach for optimizing two-phase bio-oxidations of alkanes with high reproducibility
publisher BMC
series Microbial Cell Factories
issn 1475-2859
publishDate 2017-10-01
description Abstract Background Numerous challenges remain to achieve industrially competitive space–time yields for bio-oxidations. The ability to rapidly screen bioconversion reactions for characterization and optimization is of major importance in bioprocess development and biocatalyst selection; studies at conventional lab scale are time consuming and labor intensive with low experimental throughput. The direct ω-oxyfunctionalization of aliphatic alkanes in a regio- and chemoselective manner is efficiently catalyzed by monooxygenases such as the AlkBGT enzyme complex from Pseudomonas putida under mild conditions. However, the adoption of microscale tools for these highly volatile substrates has been hindered by excessive evaporation and material incompatibility. Results This study developed and validated a robust high-throughput microwell platform for whole-cell two-liquid phase bio-oxidations of highly volatile n-alkanes. Using microwell plates machined from polytetrafluoroethylene and a sealing clamp, highly reproducible results were achieved with no significant variability such as edge effects determined. A design of experiment approach using a response surface methodology was adopted to systematically characterize the system and identify non-limiting conditions for a whole cell bioconversion of dodecane. Using resting E. coli cells to control cell concentration and reducing the fill volume it is possible to operate in non-limiting conditions with respect to oxygen and glucose whilst achieving relevant total product yields (combining 1-dodecanol, dodecanal and dodecanoic acid) of up to 1.5 mmol g DCW −1 . Conclusions Overall, the developed microwell plate greatly improves experimental throughput, accelerating the screening procedures specifically for biocatalytic processes in non-conventional media. Its simplicity, robustness and standardization ensure high reliability of results.
topic Scale-down
C–H activation
Whole-cell biocatalysis
Two-liquid phase
Monooxygenase
Reproducibility
url http://link.springer.com/article/10.1186/s12934-017-0788-4
work_keys_str_mv AT johannesfkolmar customizedmicroscaleapproachforoptimizingtwophasebiooxidationsofalkaneswithhighreproducibility
AT oliverthum customizedmicroscaleapproachforoptimizingtwophasebiooxidationsofalkaneswithhighreproducibility
AT frankbaganz customizedmicroscaleapproachforoptimizingtwophasebiooxidationsofalkaneswithhighreproducibility
_version_ 1725563201342406656