Abstract
Many cyanobacteria power metabolism during dark anaerobic conditions by the catabolism of glycogen which creates adenylate energy (ATP) and NAD(P)H. The latter can be reoxidized by a reversible NiFe-hydrogenase functioning as a terminal oxidoreductase generating H 2 as byproduct. Theoretically, one glucose molecule can yield up to 12 molecules of H 2 , although this never happens in vivo. The thermodynamic preference is for glucose catabolism via the Embden-Meyerhof-Parnas (EMP) pathway (henceforth, glycolysis) which restricts the pathway yield below 4 mole H 2 per mole glucose (so-called Thauer limit). An alternate route that is not used is the oxidative pentose phosphate shunt (OPP), which theoretically can yield 3-fold more NAD(P)H than glycolysis. Herein, we engineer the cyanobacterium Synechococcus sp. PCC 7002 to redirect glycogen catabolic flux through OPP by deleting the gap1 gene for glyceraldehyde-3-phosphate dehydrogenase (GAPDH-1) and stack this with a knock-out mutation of NADH-consuming lactate dehydrogenase (ldhA). The resulting Δgap1ΔldhA double mutant when combined with the elimination of H 2 uptake by continuous electrochemical removal of H 2 was able to produce 681 μmol H 2 per g DW per day, equivalent to 6.4 mole H 2 per mole glucose, well beyond the Thauer limit. This achieves the highest in vivo autofermentative H 2 production yield of any bacterium, equivalent to 80% of the theoretical maximum of 8 H 2 per glucose via OPP, using only photoautotrophically generated glycogen as precursor with full retention of cellular viability. These findings demonstrate the plasticity of central carbon metabolism and the significant potential of metabolic engineering for redirecting carbohydrate catabolism towards hydrogen production in cyanobacteria.
| Original language | English |
|---|---|
| Pages (from-to) | 1035-1045 |
| Number of pages | 11 |
| Journal | Energy and Environmental Science |
| Volume | 12 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - Mar 1 2019 |
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ASJC Scopus subject areas
- Environmental Chemistry
- Renewable Energy, Sustainability and the Environment
- Nuclear Energy and Engineering
- Pollution
Cite this
Crossing the Thauer limit : Rewiring cyanobacterial metabolism to maximize fermentative H 2 production. / Kumaraswamy, Kenchappa G.; Krishnan, Anagha; Ananyev, Gennady; Zhang, Shuyi; Bryant, Donald A.; Dismukes, G Charles.
In: Energy and Environmental Science, Vol. 12, No. 3, 01.03.2019, p. 1035-1045.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Crossing the Thauer limit
T2 - Rewiring cyanobacterial metabolism to maximize fermentative H 2 production
AU - Kumaraswamy, Kenchappa G.
AU - Krishnan, Anagha
AU - Ananyev, Gennady
AU - Zhang, Shuyi
AU - Bryant, Donald A.
AU - Dismukes, G Charles
PY - 2019/3/1
Y1 - 2019/3/1
N2 - Many cyanobacteria power metabolism during dark anaerobic conditions by the catabolism of glycogen which creates adenylate energy (ATP) and NAD(P)H. The latter can be reoxidized by a reversible NiFe-hydrogenase functioning as a terminal oxidoreductase generating H 2 as byproduct. Theoretically, one glucose molecule can yield up to 12 molecules of H 2 , although this never happens in vivo. The thermodynamic preference is for glucose catabolism via the Embden-Meyerhof-Parnas (EMP) pathway (henceforth, glycolysis) which restricts the pathway yield below 4 mole H 2 per mole glucose (so-called Thauer limit). An alternate route that is not used is the oxidative pentose phosphate shunt (OPP), which theoretically can yield 3-fold more NAD(P)H than glycolysis. Herein, we engineer the cyanobacterium Synechococcus sp. PCC 7002 to redirect glycogen catabolic flux through OPP by deleting the gap1 gene for glyceraldehyde-3-phosphate dehydrogenase (GAPDH-1) and stack this with a knock-out mutation of NADH-consuming lactate dehydrogenase (ldhA). The resulting Δgap1ΔldhA double mutant when combined with the elimination of H 2 uptake by continuous electrochemical removal of H 2 was able to produce 681 μmol H 2 per g DW per day, equivalent to 6.4 mole H 2 per mole glucose, well beyond the Thauer limit. This achieves the highest in vivo autofermentative H 2 production yield of any bacterium, equivalent to 80% of the theoretical maximum of 8 H 2 per glucose via OPP, using only photoautotrophically generated glycogen as precursor with full retention of cellular viability. These findings demonstrate the plasticity of central carbon metabolism and the significant potential of metabolic engineering for redirecting carbohydrate catabolism towards hydrogen production in cyanobacteria.
AB - Many cyanobacteria power metabolism during dark anaerobic conditions by the catabolism of glycogen which creates adenylate energy (ATP) and NAD(P)H. The latter can be reoxidized by a reversible NiFe-hydrogenase functioning as a terminal oxidoreductase generating H 2 as byproduct. Theoretically, one glucose molecule can yield up to 12 molecules of H 2 , although this never happens in vivo. The thermodynamic preference is for glucose catabolism via the Embden-Meyerhof-Parnas (EMP) pathway (henceforth, glycolysis) which restricts the pathway yield below 4 mole H 2 per mole glucose (so-called Thauer limit). An alternate route that is not used is the oxidative pentose phosphate shunt (OPP), which theoretically can yield 3-fold more NAD(P)H than glycolysis. Herein, we engineer the cyanobacterium Synechococcus sp. PCC 7002 to redirect glycogen catabolic flux through OPP by deleting the gap1 gene for glyceraldehyde-3-phosphate dehydrogenase (GAPDH-1) and stack this with a knock-out mutation of NADH-consuming lactate dehydrogenase (ldhA). The resulting Δgap1ΔldhA double mutant when combined with the elimination of H 2 uptake by continuous electrochemical removal of H 2 was able to produce 681 μmol H 2 per g DW per day, equivalent to 6.4 mole H 2 per mole glucose, well beyond the Thauer limit. This achieves the highest in vivo autofermentative H 2 production yield of any bacterium, equivalent to 80% of the theoretical maximum of 8 H 2 per glucose via OPP, using only photoautotrophically generated glycogen as precursor with full retention of cellular viability. These findings demonstrate the plasticity of central carbon metabolism and the significant potential of metabolic engineering for redirecting carbohydrate catabolism towards hydrogen production in cyanobacteria.
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U2 - 10.1039/c8ee03606c
DO - 10.1039/c8ee03606c
M3 - Article
VL - 12
SP - 1035
EP - 1045
JO - Energy and Environmental Science
JF - Energy and Environmental Science
SN - 1754-5692
IS - 3
ER -