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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

The focus of this paper is to detail best practices for making media for fastidious anaerobic microorganisms acquired from an environment. These methods help manage anaerobic cultures and can be applied to support the growth of elusive uncultured microorganisms, the "microbial dark matter."

Abstract

Culture-dependent research of anaerobic microorganisms rests upon methodological competence. These methods must create and maintain suitable growth conditions (e.g., pH and carbon sources) for anaerobic microorganisms while also allowing samples to be extracted without compromising the artificial environment. To this end, methods that are informed by and simulate an in situ environment can be of great aid in culturing microorganisms from that environment. Here, we outline an in situ informed and simulated anaerobic method for culturing terrestrial surface and subsurface microorganisms, emphasizing anaerobic sample collection with minimal perturbation. This protocol details the production of a customizable anaerobic liquid medium, and the environmental acquisition and in vitro growth of anaerobic microorganisms. The protocol also covers critical components of an anaerobic bioreactor used for environmental simulations of sediment and anaerobic liquid media for environmentally acquired cultures. We have included preliminary Next Generation Sequencing data from a maintained microbiome over the lifespan of a bioreactor where the active culture dynamically adjusted in response to an experimental carbon source.

Introduction

Most microorganisms remain uncultured; this is supported by the great disparity between cells observed through microscopy contrasted by the few microorganisms successfully cultured using agar plates. Staley and Konopka named this disparity the "Great Plate Count Anomaly"1. The estimated unaccounted diversity is supported by metagenomic and metatranscriptomic data showing many novel genera distributed in rank abundance curves from several different environments2. Microorganisms that have been observed (generally by random shotgun sequencing of a microbial community) but have not been cultured....

Protocol

1. Production of customizable anaerobic liquid medium

  1. Medium for culture bottles (production of 500 mL)
    1. Measure and add compounds to a 1 L bottle and adjust the pH using the column in Table 1 corresponding to the reader's culture of interest (amounts in Table 1 are recorded for production of 1,000 mL, adjust accordingly). Mix compounds to homogeneity by swirling the bottle.
    2. Heat the liquid to boiling by microwaving the bottle for 5-.......

Representative Results

Here we show results from a bioreactor study using a borehole mixed culture medium preparation method and a bioreactor setup method as described herein. The borehole mixed culture medium was modified to contain as a carbon source a slurry of corn cobs processed by Oxidative Hydrothermal Dissolution (OHD)13,14. Modified borehole mixed culture medium was pumped into the bioreactor for 44 days at a rate of 0.4 mL/min. On day 23, an inoculum sourced from borehole BLM.......

Discussion

The medium production section of this protocol (section 1) owes its structure to the modified Hungate technique of Miller and Wolin17, which has been widely used since its publication. The practicality of this expanded protocol comes from its descriptive nature and pairing with the in situ acquisition of microorganisms. Culture bottles containing environmentally informed and simulated media have been used to successfully culture the following in situ-acquired former members of th.......

Acknowledgements

The authors would like to acknowledge the lineage of information and mentorship that has influenced/evolved these techniques over the years. Dr. Hamilton-Brehm as a former graduate student, postdoc, and current professor owes a debt of gratitude to those who took the time to teach anaerobic techniques: Dr. Mike Adams, Dr. Gerti Schut, Dr. Jim Elkins, Dr. Mircea Podar, Dr. Duane Moser, and Dr. Brian Hedlund. The Nature Conservancy and American Rivers supported this work through grants G21-026-CON-P and AR-CE21GOS373, respectively. Any opinions, findings, conclusions, or recommendations expressed in this paper are those of the authors and do not necessarily reflect the ....

Materials

NameCompanyCatalog NumberComments
General Materials
1 L borosillicate bottleFisher Scientific
1 mL syringe with slip tipFisher Scientific
10 mL glass pipetteFisher Scientific
100 mL culture bottleFisher Scientifc
20 mm hand crimperFisher Scientifc
23 G needleFisher Scientifc
500 mL borosilicate bottleFisher Scientific
Aluminum sealFisher Scientifc
Cannula, 31.5 cm lengthFisher Scientific
Cannula, 6 cm lengthFisher Scientifc
CorerGiddings Machine Company Assembled from company parts
Gas manifoldSwagelokAssembled from many different parts
LighterLowe's
N2 gasAirgas
Nitrile glovesFisher Scientific
Rubber stopper (for GL45 bottles)Glasgeratebau OCHS
Rubber stopper (for culture bottles)Ace Glass
Stirring hot plateCorning
Trace mineralsATCC
VitaminsATCC
Bioreactor-specific Materials
#10 rubber stopperAce Glass
#7 rubber stopperFisher Scientifc
1 mL syringe with luer lock tipFisher Scientifc
1/4" hose barb ball valveAmazon
10 mL syringe with luer lock tipFisher Scientifc
3.5 L borosilicate bottleFisher Scientific
5/16" - 1/4" hose barb adapter fittingAmazon
60 mL syringe with luer lock tipFisher Scientifc
8 L borosillicate carboyAllen Glass
Angled hose connector for GL14 open top capAce Glass7623-20
BalloonParty City
Borosillicate bioreactorAllen Scientific GlassCustom made upon request
DrillLowe's
Female luer lock adapter couplerAmazon
GL14 open top capAce Glass7621-04
GL18 open top capAce Glass7621-08
GL45 open top capAce Glass
PTFE faced silicone septum for GL14 open top capAce Glass7625-06
PTFE faced silicone septum for GL18 open top capAce Glass7625-07
Ring standFisher Scientific
Ring stand chain clampAmazon
Ring stand clampFisher Scientific
Silicone tubing; 1/4" id, 1/2" odGrainger55YG13
Silicone tubing; 3/16" id, 3/8" odGrainger
Straight hose connector for GL14 open top capAce Glass7623-22
Three-way stopcockAmazon
Two-way stopcockAmazon
Ultra low flow variable flow mini-pumpVWR
Water bathFisher Scientifc
White rubber septum for 13-18 mm od tubesAce Glass9096-49
WireLowe's
Zip tieLowe's

References

  1. Staley, J. T., Konopka, A. Measurement of in situ activities of nonphotosynthetic microorganisms in aquatic and terrestrial habitats. Annu. Rev. Microbiol. 39 (1), 321-346 (1985).
  2. Lloyd, K. G., Steen, A. D., Ladau, J., Yin, J., Crosby, L.

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