Microbial Fuel Cell (MFC) — Bioelectricity Generation from Acidogenic Fermentation

Although H2 produced from dark fermentation process is considered as a viable alternative fuel and energy carrier of the future, H2 storage, purification, low pro­duction rates and the requirements of separate fuel cell systems for the generation of energy (electricity) are some of the inherent limitations. Alternatively, the microbial fuel cell (MFC) facilitates in situ conversion of energy in the form of bioelectricity from wastewater treatment by dark fermentation [111, 147-158]. MFC is a hybrid bio-electrochemical system, which converts the substrate directly into electricity by the oxidation of organic matter in the presence of bacteria (bio-catalyst) at ambi­ent temperature/pressure [155, 156]. The potential developed between the bacterial metabolic activity [reduction reaction generating electrons (e-) and protons (H+)] and electron acceptor conditions separated by a membrane manifests bioelectricity generation. In an acidogenic microenvironment, single and dual chambered MFC systems were evaluated for the production of bioelectricity using various types of wastewater viz., chemical wastewater, designed synthetic wastewater, domes­tic sewage and vegetable waste employing mixed cultures as anodic biocatalysts [147-158] (Table 7). The higher activity of intracellular e — carriers which will help in the translocation of e — from bacteria to the outside of the cell might be the rea­son for higher current generation observed under acidic pH operation [156]. Apart

Table 6 Details of some studied pertaining to metabolic engineering carried out to enhance fermentative H2 production

Nature of genetic modification

Microorganism

Comments

References

Inactivating hycA gene and simultaneous overexpression of the formate hydrogen lyase activator fhlA gene

Escherichia coli

Improved H2 production

[138]

Knocking out lactate dehydrogenase

Escherichia coli

35% improvement in H2 production

[139]

Blocking the formation of alcohol and some organic acids using the proton suicide technique with NaBr and NaBrO3

Enterobacter

cloacae

Improved H2 production (3.4 mol Щ/mole of glucose)

[140]

Knocking out ackinase

Clostridium tyrobutyricum ATCC 25755

Improved H2 production (2.61 mol H2/mole of glucose)

[141]

Inactivation of hycA gene

Escherichia coli HD 701

14 fold increase in H2 production at lower glucose concentration (100 mmol)

[142]

Overexpression of its own hydA gene encoding [Fe]-hydrogenease

Clostridium

paraputrificum

M121

1.7 fold improvement in H2 production (2.4 mol H2/mole n-acetyl glucosamine)

[143]

Inactivation of acetate kinase

Clostridium

tyrobutyricum

1.5 fold improvement in H2 production (2.2 mol H2/mole glucose)

[144]

Double mutant

Eneterobacter aerogens strain AY2

2 fold improvement in H2 production (1.2 mol H2/mole glucose)

[145]

Knocking out formate hydrogen lyase (FHL) gene cluster hycABCDE in chromosomal DNA

Enterobacter

aerogenes

IAM1183

Improved H2 production (from 18.3 to 45.2%) and purity (from 59 to 71%)

[146]

Altering expression of formate hydrogen lyase (FHL) by inactivating repressor gene and overexpressing the activator gene simultaneously

Escherichia coli K12

4 fold improvement in H2 production

[147]

from power generation, the MFC also demonstrated an enhanced substrate degrada­tion rate along with good color and total dissolved solid (TDS) removal efficiency compared to conventional anaerobic treatment [156]. MFCs can also utilize acid — rich carbon effluents generated from acidogenic processes as primary substrate for bioelectricity generation along with additional treatment efficiency.