Enterobacter cloacae

HOW TO TRANSFORM AND CULTURE

  • The complete E. cloacae subsp. cloacae ATCC 13047 genome contains a single circular chromosome of 5,314,588 bp and two circular plasmids, pECL_A and pECL_B, of 200,370 and 85,650 bp (GenBank accession numbers CP001918, CP001919 and CP001920, respectively).[34]
  • The other genomes of E. cloacae that have been sequenced are deposited in GenBank under accession numbers CP002272, CP002886, FP929040 and AGSY00000000.
  • Complete Genome Sequence of Enterobacter cloacae subsp. cloacae Type Strain ATCC 13047: http://jb.asm.org/content/192/9/2463.long
  • Culture conditions:
    • For microbial fuel cell: Aerobically grown, 30 °C, attach bacteria to solid anode surface to form biofilm, sparged with N2 gas
    •  

METABOLISM

  • Pure cultures on cellulose produce predominately acetate, as well as various volatile fatty acids and solvents
    • “Therefore, while this strain can both degrade cellulose and produce electricity, it cannot fully utilize some breakdown products for power generation. Complete utilization of the carbon sources in an MFC, therefore, would still require addition of other microbial strains to the culture or genetic modification of E. cloacae to use these substrates” – opportunity for improvement
    • “The current densities produced by the mixed culture during the last three serial transfers was higher than that produced by either strain of E. cloacae. The reason for this is not known, but it is likely that other bacteria in the mixed community were able to use breakdown products produced by E. cloacae for power generation”
    • E. cloacae cannot use lactate, acetate, or butyrate for power generation
    • E. cloacae can generate power from sugars (glucose and sucrose) and glycerol, and can ferment glucose, sucrose, and cellobiose to produce hydrogen

Biochemical characteristics of E. cloacae ATCC 13047T and E. cloacae FR

Carbon source and electron donor

Utilization by:

E. cloacae ATCC 13047T

Isolate FR

Dextrin

+

+

Glycogen

+a

+a

N-Acetyl-D-glucosamine

+

+

D-Cellobiose

+

+

L-Arabinose

+

+

Gentiobiose

+a

+a

D-Glucose

+a

+a

D-Lactose

+

+

Sucrose

+

+

Acetic acid

+a

+a

cis-Acontic acid

+

+

Citric acid

+

+

Formic acid

+a

+a

Lactic acid

+

+

Glycerol

+

+

a Weak.

NITROGEN FIXATION

  • Cloning, nucleotide sequence, and expression of the nitroreductase gene from Enterobacter cloacae: http://www.jbc.org/content/266/7/4126.short
  • Diazotrophic Mixed Cultures of Azospirillum Brasilense and Enterobacter Cloacae:

Coculture of A. brasilense and E. cloacae on semi-solid medium showed two compartments, one for each bacterium, and led to efficient nitrogen fixation. A. brasilense in the culture grew and fixed nitrogen using the fermentation products produced by E. cloacae, including acetic and succinic acids, acetoin and 2,3-butanediol.

http://download-v2.springer.com/static/pdf/653/chp%253A10.1007%252F978-3-642-79906-8_21.pdf?token2=exp=1429414860~acl=%2Fstatic%2Fpdf%2F653%2Fchp%25253A10.1007%25252F978-3-642-79906-8_21.pdf*~hmac=c59f4a42b93bcc375830a36ead0b455d50562d426d20c80d634f15a4f66af560

http://link.springer.com/chapter/10.1007/978-3-642-79906-8_21

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ELECTRICITY PRODUCTION – MICROBIAL FUEL CELL

HYDROGEN PRODUCTION

ETHANOL PRODUCTION

MODELING AND COCULTURES:

QUESTIONS:

  • Can we grow the bacteria in an anaerobic environment?
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