Lack of Protective Osmolytes Limits Final Cell Density and Volumetric Productivity of Ethanologenic Escherichia coli KO11 during Xylose Fermentation

Microorganisms and media.Ethanologenic E. coli KO11 [frd cat pfl⁺ pfl::(Z. mobilis pdc⁺ adhB⁺)] (37) and SU102 (KO11 ΔackA) (46) are prototrophic and were grown in CSL medium containing the following ingredients (per liter): 90 g of xylose, 10 g of corn steep liquor (∼50% dry weight), 1 g of KH₂PO₄, 0.5 g of K₂HPO₄, 3.1 g of (NH₄)₂SO₄, 0.4 g of MgCl₂ · 6H₂O, and 20 mg of FeCl₃ · 6H₂O (45). Solid medium contained 1.5% agar, 20 g of xylose liter⁻¹, and chloramphenicol (40 to 600 mg liter⁻¹). Working cultures were transferred daily on solid medium. Stock cultures were stored frozen at −75°C in 40% glycerol. No antibiotics were added to broth cultures.

Stock solutions of glutamate, acetate, proline, betaine, dimethylsulfoniopropionate, and taurine were dissolved in deionized water, neutralized as required (NaOH, H₂SO₄, or NaHCO₃) and sterilized by filtration. All osmoprotectants were purchased from Sigma (St. Louis, Mo.) except dimethylsulfoniopropionate (TCI America, Portland, Oreg.). Corn steep liquor was purchased from the Grain Processing Corporation (Muscatine, Iowa).

Aerobic growth studies.Colonies were transferred from solid medium to baffled flasks (1 liter) containing 250 ml of CSL medium (initial cell concentration of ∼3 mg [dry weight] of cells liter⁻¹) and incubated at 35°C (220 rpm).

Fermentation.Seed cultures and fermentations were performed in CSL medium at 35°C (pH 6.5, 120 rpm) as described previously (34, 45). Fermentations were inoculated to provide an initial cell density of 33 mg (dry weight) liter⁻¹.

¹³C NMR.Intracellular osmolytes were analyzed by NMR as previously described (37). Cells were harvested in late exponential phase. Cell pellets from 700 ml of broth (∼24 h for anaerobic; ∼12 h for aerobic) were washed twice in the mineral salts component of CSL medium containing additional NaCl (600 mM) and extracted with 3 volumes of 95% ethanol. Suspensions were rocked gently for 16 to 24 h at 4°C. Debris was then removed by centrifugation (4°C, 10,000 × g, 30 min). Extracts were dried under vacuum twice to remove all traces of ethanol, dissolved in 4.0 ml of 25% D₂O, and filtered (0.2-μm-pore-size filter). Acetone (10 μl) was added as an internal reference. NMR spectra were obtained using a modified Nicolet NT300 spectrometer operating in the Fourier transform mode as follows: 75.46 MHz; excitation pulse width, 25 μs; pulse repetition delay, 40 s; spectral width, 18 kHz; and broadband (bilevel) decoupling of protons (>1,000 scans) (38). Osmolyte pools were estimated using a standard curve for each compound with acetone as the internal standard. Intracellular pools are reported in nanomoles per milliliter per optical density at 550 nm [OD₅₅₀] unit as described by Csonka et al. (14).

Analytical methods.For fermentation studies, cell mass was estimated from OD₅₅₀ using a Bausch & Lomb Spectronic 70 spectrophotometer and a weight calibration curve (1 OD₅₅₀ unit = 0.33 g [dry weight] of cells liter⁻¹). Ethanol was measured by gas chromatography (Varian 3400CX) (34).

Comparison of intracellular osmolytes in E. coli KO11 during aerobic and anaerobic growth.During aerobic growth in CSL medium (9% xylose, 600 mM), E. coli KO11 grew to more than twice the cell density of cultures grown anaerobically in the same medium with or without additional minerals and trace metals (Fig. 2A) (45). ATP production does not appear to limit anaerobic growth in 9% xylose (45, 46), since cell densities achieved with xylose (<0.5 ATP molecule per glucose molecule) were equivalent to those with glucose (>2.0 ATP molecules per glucose molecule). The lower cell mass during anaerobic growth limited volumetric ethanol productivity, increasing the time required to complete fermentation (45).

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FIG. 2.

Fermentation of xylose by E. coli KO11 in CSL medium containing various supplements. (A) Effects of conditions and mutations that promote glutamate synthesis. (B) Effects of protective osmolytes on E. coli KO11. Unless indicated otherwise, all cultures were anaerobic. Maximum cell mass (white bars) and average volumetric productivity of ethanol (black bars) (initial 72-h period) are shown. Values are averages ± standard deviations (error bars) of two or more experiments. Abbreviation: DMSP, dimethylsulfoniopropionate.

An NMR comparison of major intracellular osmolytes during aerobic and anaerobic growth revealed striking differences (Table 1; Fig. 3A and B). During aerobic growth, high levels of glutamate (17.0 nmol ml⁻¹ OD₅₅₀ unit⁻¹), trehalose (9.9 nmol ml⁻¹ OD₅₅₀ unit⁻¹), and betaine (19.8 nmol ml⁻¹ OD₅₅₀ unit⁻¹) were present, consistent with adaptation to the highly osmotic environment in unmodified strains of E. coli (5, 27). Although E. coli is incapable of de novo betaine synthesis, this protective osmolyte can be synthesized under aerobic conditions (only) by oxidizing choline (26), which is present in corn steep liquor (Traders' guide to fermentation media formulation, Traders Protein, Memphis, Tenn.). Choline cannot be oxidized to betaine during fermentative growth.

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FIG. 3.

¹³C NMR spectra of intracellular osmolytes from ethanologenic E. coli KO11. (A) KO11 during fermentation without additives; (B) KO11 during aerobic growth without additives; (C) KO11 supplemented with 11 mM (2 g liter⁻¹) potassium glutamate during fermentation; (D) KO11 supplemented with 24 mM (2 g liter⁻¹) sodium acetate during fermentation; (E) SU102 (ΔackA) fermentation without additives; (F) KO11 expressing CitZ, an NADH-insensitive citrate synthase from B. subtilis; (G) KO11 supplemented with 2 mM betaine during fermentation; (H) KO11 supplemented with 0.25 mM dimethylsulfoniopropionate during fermentation. Peaks are labeled as follows: A, acetone; P, proline; G, glutamate; B, betaine; D, dimethylsulfoniopropionate; and T, trehalose. The scale is in parts per million.

During anaerobic growth, proline (71.9 nmol ml⁻¹ OD₅₅₀ unit⁻¹) was the only osmolyte above our limit of detection (≤4.0 nmol ml⁻¹ OD₅₅₀ unit⁻¹). Since allosteric regulation prevents the biosynthesis of proline as an osmoprotectant (12, 41, 42), it is likely that corn steep liquor is also the source of intracellular proline. Supplementing CSL medium with additional proline (17 mM) had no effect on cell growth or volumetric productivity despite a 14% increase in the intracellular pool. Although proline accumulation is presumed to be beneficial as an osmolyte, it is typically less effective than betaine as an adaptation to osmotic stress (30, 40). The absence of trehalose (<4.0 nmol ml⁻¹ OD₅₅₀ unit⁻¹) during anaerobic growth in CSL medium is also noteworthy. The relatively low ATP yield from xylose catabolism (0.4 ATP molecule per pyruvate molecule [43, 45]) may serve to restrict gluconeogenesis and trehalose production during fermentation.

Supplementing CSL medium with glutamate during fermentation increased the concentration of cells by 87% (Fig. 2B) and increased the glutamate pool (16.2 nmol ml⁻¹ OD₅₅₀ unit⁻¹) to that present during aerobic growth (17.0 nmol ml⁻¹ OD₅₅₀ unit⁻¹), with a corresponding decrease in proline (Table 1; Fig. 3C). These results demonstrated that both limited cell growth and low volumetric productivity correlate with a small intracellular pool of glutamate, consistent with a deficiency of glutamate for osmoprotection (45, 46).

Citrate synthase flux limits the intracellular accumulation of glutamate.Insufficient carbon partitioning into 2-ketoglutarate, the immediate precursor of glutamate (Fig. 1), has been proposed to limit E. coli KO11 cell mass (and volumetric productivity) during anaerobic growth (high NADH/NAD⁺ ratio) in CSL medium, consistent with a small glutamate pool (Table 1). Citrate synthase is a key allosteric enzyme at the committed branch point for 2-ketoglutarate synthesis (48) (Fig. 1). Allosteric inhibition of this native enzyme by high NADH levels such as those associated with anaerobic growth (16) can be antagonized by acetyl-CoA (49). Two independent approaches that have been previously used to increase the availability of acetyl-CoA (and thereby promote cell growth) were investigated for their effects on the glutamate pool during fermentations in the CSL medium: (i) supplementing with 24 mM acetate (25, 46) and (ii) inactivating the primary anaerobic acetate production pathway (ΔackA) (25, 46). Both approaches increased the glutamate pool to levels similar to that observed during aerobic growth (Table 1; Fig. 3D and E), consistent with an increase in citrate synthase activity in vivo. Cell mass and average volumetric productivity were increased by approximately twofold (Fig. 2A).

The primary citrate synthase in B. subtilis (CitZ) is insensitive to NADH and is allosterically regulated by ATP (24). Expression of B. subtilis citZ also doubled cell mass, increased volumetric productivity (Fig. 3A), and increased the intracellular glutamate pool (17.5 nmol ml⁻¹ OD₅₅₀ unit⁻¹) (Table 1; Fig. 3F). Thus, all approaches that increased the intracellular pool of glutamate were also beneficial for cell growth and ethanol production. The beneficial effects of a large intracellular pool of glutamate are consistent with the adaptation to osmotic stress as previously characterized in unmodified E. coli (13).

Deletion of ackA also eliminated ATP production by this pathway and improved growth, providing further evidence that cell growth is not ATP limited under our conditions.

Added osmoprotectants supplant the glutamate requirement.If the primary role of a large glutamate pool (resulting in increased cell growth and higher volumetric productivity) is osmoprotection, alternative protective osmolytes should provide a similar benefit and eliminate the need to alter carbon partitioning. To test this hypothesis, four different osmolytes were investigated (Table 1; Fig. 2B). The addition of taurine and proline, relatively poor osmoprotectants for E. coli (31), had no effect on final cell density or volumetric productivity. Taurine was not accumulated in cells, and proline levels were essentially the same with or without a proline supplement. Betaine and dimethylsulfoniopropionate, both excellent osmoprotectants for E. coli (7, 40), accumulated in the cytoplasm, with a corresponding reduction in proline (Fig. 2G and H). Both additives increased final cell density and volumetric productivity (Fig. 2). Since neither compound is known to be metabolized by E. coli, betaine and dimethylsulfoniopropionate are presumed to act directly as osmoprotectants.

Cell mass and volumetric productivity were dose dependent for each additive with optima of approximately 2.0 mM for betaine and 0.25 mM for dimethylsulfoniopropionate (Fig. 4). Thus, dimethylsulfoniopropionate acts as a more effective osmolyte than betaine during xylose fermentation. In contrast, previous studies have identified betaine as the most effective osmolyte for salt stress (7, 40). Under aerobic conditions, the effectiveness of betaine in promoting growth has been reported to vary in response to osmotic stress with different sugars (19). The relative effectiveness of specific protective osmolytes appears to be dependent on the nature of the stressing agent (sugars and salts) and the growth conditions.

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FIG. 4.

Effects of betaine and dimethylsulfoniopropionate on E. coli KO11 growth and ethanol production. (A and B) Effects of betaine on growth (A) and ethanol production (B). (C and D) Effects of dimethylsulfoniopropionate on growth (C) and ethanol production (D). Symbols: ▪, no addition; ▴, 0.1 mM; •, 0.25 mM; ▵, 0.5 mM; ○, 1.0 mM; □, 2.0 mM.

Betaine was the only osmolyte detected in cells from fermentations supplemented with betaine (Fig. 3G; Table 1), consistent with a low K_m for betaine transport (6, 28, 39). Both betaine and proline are concentrated from the medium by the same transporters, ProP and ProU (28). The high level of betaine in the medium (2.0 mM) coupled with the low K_m of the primary betaine transport pathway (ProU) is consistent with exclusion by the preferential transport of betaine. Added taurine was not accumulated in cells and may be similarly excluded by the preferential transport of proline in corn steep liquor.

Cells from fermentations supplemented with 0.25 mM dimethylsulfoniopropionate accumulated both proline and dimethylsulfoniopropionate. Although little is known about dimethylsulfoniopropionate transport, the osmotically activated transporters (ProP and ProU) are known to be promiscuous, transporting proline, taurine, ectoine, betaine, and other structurally analogous compounds (21, 23, 28, 31, 39). Presumably, dimethylsulfoniopropionate is also transported by ProU and ProP. The lower extracellular concentration of dimethylsulfoniopropionate (0.25 mM) compared to betaine (2.0 mM) appears to allow the accumulation of intracellular pools of both proline and dimethylsulfoniopropionate.

Glutamate was not detected in cells grown in CSL medium with either betaine or dimethylsulfoniopropionate as a supplement (Table 1; Fig. 3G and H), confirming that a large glutamate pool per se is not required to increase final cell density and volumetric productivity. Thus, the apparent requirement for additional glutamate during fermentation in CSL medium can be directly attributed to a requirement for osmotic adaptation. Under these conditions, cell growth is limited by insufficient levels of an effective osmolyte, rather than a nutritional requirement for glutamate during biosynthesis.

Conclusions.The limited cell growth and accompanying low volumetric productivity of ethanologenic E. coli KO11 during xylose fermentation in CSL medium can be attributed to osmotic stress and inadequate levels of protective osmolytes. Inactivation of acetate kinase (ΔackA), supplementing with acetate, supplementing with glutamate, and expression of B. subtilis citZ were each shown to increase the partitioning of carbon into the citrate arm of the anaerobic TCA pathway, as evidenced by an increase in the intracellular glutamate concentration. All approaches that increased the intracellular pool of glutamate also increased final cell density and volumetric productivity. The apparent requirement for glutamate was completely eliminated by supplementing with alternative osmoprotectants (dimethylsulfoniopropionate or betaine), demonstrating that this requirement is related to osmotic stress rather than to a specific biosynthetic need.