A versatile method for preparation of hydrated microbial–latex biocatalytic coatings for gas absorption and gas evolution

Author:

Gosse Jimmy L12,Chinn Mari S1,Grunden Amy M3,Bernal Oscar I4,Jenkins Jessica S4,Yeager Chris5,Kosourov Sergey6,Seibert Michael6,Flickinger Michael C7

Affiliation:

1. grid.40803.3f 0000000121736074 Department of Biological and Agricultural Engineering North Carolina State University 277D.S. Weaver Labs 27695 Raleigh NC USA

2. BioCee, Inc. 1479 Gortner Ave Suite 322 55108 St. Paul MN USA

3. grid.40803.3f 0000000121736074 Department of Microbiology North Carolina State University 4550 Thomas Hall 27695 Raleigh NC USA

4. grid.40803.3f 0000000121736074 Department of Chemical and Biomolecular Engineering North Carolina State University 911 Partners Way 27695 Raleigh NC USA

5. grid.451247.1 0000000403674086 Environmental Sciences and Biotechnology Savannah River National Laboratory Building 999-W 29808 Aiken SC USA

6. grid.419357.d 0000000121993636 Energy Sciences Directorate, National Renewable Energy Laboratory 1617 Cole Blvd. 80401 Golden CO USA

7. grid.40803.3f 0000000121736074 Department of Chemical and Biomolecular Engineering, Golden-LEAF Biomanufacturing Training and Education Center North Carolina State University Campus Box 7928 27695 Raleigh NC USA

Abstract

Abstract We describe a latex wet coalescence method for gas-phase immobilization of microorganisms on paper which does not require drying for adhesion. This method reduces drying stresses to the microbes. It is applicable for microorganisms that do not tolerate desiccation stress during latex drying even in the presence of carbohydrates. Small surface area, 10–65 μm thick coatings were generated on chromatography paper strips and placed in the head-space of vertical sealed tubes containing liquid to hydrate the paper. These gas-phase microbial coatings hydrated by liquid in the paper pore space demonstrated absorption or evolution of H2, CO, CO2 or O2. The microbial products produced, ethanol and acetate, diffuse into the hydrated paper pores and accumulate in the liquid at the bottom of the tube. The paper provides hydration to the back side of the coating and also separates the biocatalyst from the products. Coating reactivity was demonstrated for Chlamydomonas reinhardtii CC124, which consumed CO2 and produced 10.2 ± 0.2 mmol O2 m−2 h−1, Rhodopseudomonas palustris CGA009, which consumed acetate and produced 0.47 ± 0.04 mmol H2 m−2 h−1, Clostridium ljungdahlii OTA1, which consumed 6 mmol CO m−2 h−1, and Synechococcus sp. PCC7002, which consumed CO2 and produced 5.00 ± 0.25 mmol O2 m−2 h−1. Coating thickness and microstructure were related to microbe size as determined by digital micrometry, profilometry, and confocal microscopy. The immobilization of different microorganisms in thin adhesive films in the gas phase demonstrates the utility of this method for evaluating genetically optimized microorganisms for gas absorption and gas evolution.

Publisher

Oxford University Press (OUP)

Subject

Applied Microbiology and Biotechnology,Biotechnology,Bioengineering

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