Patent Application
20150087049
This application claims the benefit of German Application No. DE 102013015969.5 filed on Sep. 25, 2013; the German priority application is incorporated by reference herein in its entirety.
At low biomass concentrations cyanobacteria and micro-algae reveal high specific rates of the photoautotrophic growth (up to more than 3 d−1) and exhibit a high potential for bioprocess techniques to produce biomass or valuable organic materials (foods or animal feeds, drugs, biofuels) by photosynthesis. Axenic research culture of photoautotrophic microorganisms (PMO) is carried out mainly in shaken culture vessels exposed to the light or in vessels wherein a flow of bubbles containing air enriched with CO2 is rising up, while the entrance of foreign organisms is prevented by bacterial filters.
Photobioreactors for use in laboratories (research-photobioreactors) have been developed for standardization and optimization of the conditions controlling photoautotrophic growth. However, independent of the volume of the reaction vessels, it is difficult to ensure the provision of PMO with nutrients, CO2 and light in such a manner that a high biomass concentration can be reached and intensive growth is possible at high biomass concentrations. A concentration of the dehydrated biomass (DB) above 5 μl−1 has to be designated as extremely high at the culture of PMO (e.g. Wang et al. 2012). ‘Besides the maintenance of saturating concentrations of inorganic carbon or other miner nutrients in the culture medium it is required to supply light quanta to all cells and to avoid oxidative stress in order to obtain a high rate of photosynthesis referred to the volume of the cell suspension or to the area exposed to light. According to the present art, extremely high concentrations of dehydrated biomass (CDB) can be obtained in short time, when cell suspensions of relatively low thickness (below 2 cm) are put in turbulent flow at photon flux densities (PFD) above 1 mmol m−2 s−1. Even at extremely high PFD (several mmol m−2 s−1) at the exposed surface of a dense cell suspension, the thickness of the surface layer, wherein the PFD is above the light compensation point (photic zone) is reduced to less than 0.1 cm. For reaching a high quantum yield it is essential that the cells are circulating with a high frequency between the photic zone and the non-avoidable aphotic zone. This way, the mean duration of the aphotic phases and phases of exposition to powered light is reduced and the high PFD can be utilized efficiently by all cells. If the dark phases are very short (millisecond range), they can be utilized for the carbon reduction by using the chemi-osmotic potential that can be stored by the thylakoids in darkness for very short time. In addition, the continuous interruption of the exposition to powered light prevents or shortens the hold up periods in the electron transport chain which might create oxidative stress (Quiang et al. 1998, Pulz 0 2012) In the few studies reporting on rapid photoautotrophic growth at an extremely high cell density with an increase of CDB >4 g l−1 d−1 at a CDB >5 g L−1 (Quiang et al. 1998, Doucha und Livansky 2006), the turbulent flow of the cell suspension was realized in open (non-axenic) systems by gas bubble flow with high velocity or by a high rate of the gravity driven flow rate of the suspension on an inclined flow bed. At exposition to high powered light with a maximum light path of 7 mm, photosynthesis rates of almost 200 g s−1 per m2 of the exposed area have been established in a suspension of the cyanobacterium Spirulina platensis for a short period (5 h). Here, the growth limitation by chemical factors (inorganic C and further nutrient dissolved elements) was prevented by a suitable medium. In the open systems exhibiting an intensive gas exchange with the outer gaseous atmosphere it is possible to prevent the enrichment of O2 in the cell suspension; however, a strong wasting of water by evaporation has to be compensated and the major part of the CO2 introduced is loosed by the gas exchange with the atmosphere. The substitution of the consumed inorganic C (Ci) in the cell suspension was carried out by delivery of CO2 from the gaseous phase across the agitated gas-liquid interface (Quiang et al. 1998) or by dissolution of compressed CO2 (Doucha und Livansky 2006).
Using closed research photobioreactors that are applicable for the axenic culture of PMO at a high cell density (Tsoglin et al., 1995), somewhat lower rates of photosynthesis referred to the exposed area were achieved. In these cases turbation and gas mass transfer was caused by means of a rotor or by shaking. Here however, it happened that the O2 partial pressure in the closed reaction chamber increased strongly and finally reached growth-inhibiting values.
Besides the already mentioned mass transfer through the turbulent gas-liquid-interface or the dissolution of compressed carbon dioxide, the introduction of carbonized water, the delivery of HCO3− ions from a cell-free carbon storage medium through a dialysis membrane (DE 2013/102011055481) or the delivery of CO2 by diffusion across a gas-permeable hydrophobic films or membranes (e.g. US 2004/6,815,204 B2, US 2009/0305389 A1, US 2009/0130704 A1, DE 2009/102008029) are known methods of feeding Ci. A research cultivation system for PMO has been described in DE2009/10 2008 029. According to this method a bag produced from a thin translucent polyethylene film is filled with a concentrated KHCO3 containing buffer solution and introduced into the shaken culture vessel. Here the utilized Ci is substituted by diffusion of CO2 across the translucent thin polyethylene film. The growth rates reached with this device were markedly higher than those obtained at shaking the vessels at the air atmosphere. However, this culture system is not suitable for reaching extremely high cell densities (CDB >5 g l−1), since the CO2 permeability of the applied (translucent) polyethylene films is not high enough for this purpose.
The invention applies to a research-photobioreactor for the growth at extremely high cell densities in axenic cultures of cyanobacteria and microalgae exposed to a high light intensity. A hydrophobic gas-permeable first membrane 3 situated at the bottom of the reaction chamber 2 serves for the entry of CO2 into the cell suspension. The first membrane separates the CO2 containing gaseous phase in a basis chamber 1 from the cell suspension that covers the membrane. It has a permeability coefficient for the gases of air which many times surpasses the physically feasible rate of absorption of these gases in water. The turbulent flow within the cell suspension required for a high quantum yield is obtained by shaking. A high shearing rate hereby realized increases the CO2 absorption rate in the liquid phase close to the membrane, thus avoiding C-limitation even at an extremely high volume-based rate of photosynthesis. A porous hydrophobic gas-permeable second membrane 4 separates the reaction chamber 5 from at least one gas exchange chamber 6. The gas exchange chamber is connected with the outer gas atmosphere by means of at least one diffusion limiting channel 7 with a width above 0.01 cm.
The common gas diffusion resistance of all channels 7 is a manifold of the gas diffusion resistance of the second gas-permeable membrane. The surface area A of the reaction chamber A exposed to light as well as the length L and the cross sectional area Q of all channels are chosen such that the geometric factor F=A/Σ(QnLn−1) has a value between 20 and 1000 cm. The gas volume flux through a channel can be determined as measure for the actual photosynthetic turnover. The research-photobioreactor or the reaction chamber may be produced as disposable good. Using the research-photobioreactor according to the invention at a photon flux density of 850 μmol m−2 s−1, a volume-based rate of the increase in the dehydrated biomass amounting to more than 10 g l−1 d−1 was obtained corresponding to an increase of the dehydrated biomass amounting to more than 40 g m−2 d−1, if referred to the area exposed to light.
The duty of the invention consists in providing a closed research PBR that is suitable for the axenic culture of PMO with little loss of water and CO2 and by means of which a daily increase of the dehydrated biomass (DB) of more than 50% is possible at a CDB of more than 10 g l−1 preventing the rise of the O2 concentration in the cell suspension to growth-limiting values. This duty is achieved by providing a research PBR according to claim 1. The sub-claims relate to favorable embodiments of the research PBR according to the invention.
According to the invention the research-PBR has the following characteristics (
Both the undesired diffusive losses of CO2 and water vapor and the increase of the O2 partial pressure in the reaction chamber mediated by the photosynthetic reaction depend on the channel length(s) Ln and the channel cross-sectional area(s) Qn. According to the invention the gas diffusion resistance between the PBR and the atmosphere is controlled by the choice of geometric channel dimensions that together define a resistance factor F. F is an expression of the common resistance to diffusive gas exchange between the atmosphere and the reaction chamber that is referred to the exposed surface area. F is defined by the equation mentioned above. According to the invention, the channel parameters Ln and Qn are adapted to the exposed surface A area to obtain a value of F between 20 and 1000 cm.
Even at the mentioned upper limit of the F value, the resistance of the channel(s) for the viscous flow of air is so small that the pressure difference between the reaction chamber and the atmosphere is negligible. While the advantage of low F values consists in a rapid diffusion exchange of O2 and N2 between the outer atmosphere and reaction chamber, higher F values are favorable by stronger limitation of the water vapor and CO2 losses to the atmosphere. Research PBR with channel dimension according to a F value close to the mentioned upper limit (1000 cm) cannot prevent a strong increase in the O2 partial pressure in the reaction chamber at extremely high rates of photoautotrophic DB production (>20 g m−2 d−1). However, water vapor losses are negligible at such high F values. More technically significant undesired loosing of water vapor and CO2 is expectable, when F falls below the mentioned lower limit (20 cm). These relationships are exemplified in more detail by the execution example 1.
The research PBR according to the invention can be produced in such a way that the F value is adjustable. For example, when multiple channels are present, this is possible by closing/opening of a part of the channels. When the channel is built as a slit, the F value can be altered by partial closure of the slit.
To obtain a high rate of the CO2 entry into the suspension at a given CO2 concentration in the basis chamber, it is favorable, when the first membrane has an area as large as possible and is fixed to the basis of the reaction chamber in such a way that the shearing rate in the liquid phase close to the membrane is as high as possible. To reach a sufficiently high rate of the CO2 entry into the cell suspension it is essential that the permeable membrane area comprises at least 30 percent of the reaction chambers basis area. Further it is favorable, when the permeable membrane area is located above, not below, the perforations in the basal board of the reaction chamber. An arrangement of the membrane on a gas-permeable porous support layer above the perforated basic board of the reaction chamber is favorable. In this respect, any solid support layer owning high gas permeability in vertical and horizontal direction is designated as gas-permeable support layer. When such a support layer is applied, it is possible to ensure that the gas-saturated area of the first membrane reaches more than 90 percent of the basic area of the reaction chamber, even when the cross sectional area of the perforations is relatively small. This way the area of the first membrane, which is saturated with the gaseous phase of the basis chamber, can reach the value of the reaction chamber surface exposed to the light.
The basis chamber can for instance contain CO2 with a partial pressure above 1 kPa in it's predominantly gas (air) filled volume. The saturation of the atmosphere in the basis chamber can be achieved by filling some liquid water therein. By means of a reducing valve and a narrow gas inlet, the volume in the basis chamber can be connected to a source of pure CO2. The set pressure of the reducing valve can be adjusted to a value according to the atmosphere pressure. By means of the reduction valve it is ensured that the partial pressure of CO2 in the reaction chamber is maintained in the range of the set value even at rapid dissolution of CO2 in the liquid phase of the reaction chamber.
The same result can also be achieved without gas volume flux from outside, when the CO2 partial pressure within the basis chamber is maintained by a weakly alkaline buffer solution containing HCO3− in high concentration. Such buffer solutions are known since a long time as source for providing CO2 to PMO in experimental vessels (Warburg O und Rippel G 1960). When for instance a buffer solution consisting of 3 M KHCO3 und 3 M K2CO3 is situated in the basis chamber, one can maintain a CO2 concentration between 1 and 10% (vol/vol) (partial pressure 1-10 kPa) in its gaseous phase for several days even at a high rate of photosynthesis. At the highest measured value of the C-turnover referred to the area exposed to light (Quiang et al 1998) an amount of CO2 close to 60 mmol per day would be detracted from the basis chamber of a research PBR with an exposed surface area of 1 dm2. A manifold of this amount can be delivered by a volume of 300 ml of the mentioned 3 M buffer solution located in the basis chamber without a significant increase in the buffer pH or a significant reduction of the CO2 partial pressure. The carbon stored in the mentioned buffer can be more completely utilized when the pH value of the buffer is fixed by adding an acid by means of a suitable control unit.
When a weakly alkaline milieu (pH 8.5-10.5) is maintained within the cell suspension by the metabolism of the cells or by a suitable buffer, this is favorable for the growth of numerous PMO. In this case, the major part of Ci dissolved in the cell suspension is existent in the form of HCO3−. This way a strong gradient of the CO2 concentration in the liquid close to the membrane can be maintained even at a low rate of the actual photosynthetic CO2 consumption.
A favorable characteristic of the research-PBR according to the invention consists in the fact, that the metabolic O2 production is the sole significant source of a stationary viscous gas flow out of the reaction chamber into the outer atmosphere. It is, therefore, possible to measure the volume flow out of the gas exchange compartment into the atmosphere as measure of the actual photosynthetic turnover rate in a research PBR with the manifested characteristics. If for instance, a capillary tube is connected to a channel, the volume flux through this tube can be determined as measure of the actual photosynthesis rate. A simple possibility for such measurement is explained in the execution example 2.
When concentrated HCO3− containing buffer solutions with a concentration of the alkali ions above 3 M are applied to maintain the CO2 concentration in the basis chamber, the partial pressure of water vapor above this buffer is markedly lower than that in equilibrium with the cell suspension at the same temperature. In the isothermal case a transport of water vapor from the cell suspension across the first membrane into the buffer solution is not avoidable. At 30° C. this would result in a water loss amounting to some percent of the suspension volume per day. For an accurate measuring of the biomass production, it is therefore, essential to measure the water loss besides the measurement of the CDB. The volume change by isothermal distillation of water from the cell suspension to the buffer solution can be avoided or strongly diminished by maintaining a difference between the temperature of the buffer solution in the basis chamber and the temperature of the cell suspension in the reaction chamber. By thermal approaching the absolute partial pressure of water vapor in the basis chamber to that in the cell suspension, it is possible to prevent or reduce the osmotically mediated process of water vapor distillation across the first membrane. The required temperature difference can be obtained by means of an electric heater. A further possibility for creation of such a temperature difference consists in fortification of the cooling facility used for deduction of the radiant heat from the reaction chamber. This will be explained in the execution example 2.
Due to the limiting role of gas absorption at the gas-liquid-interface it is favorable, when the first membrane shares a large portion of the basis area of the reaction chamber. However, one can abstain from a large area of the second membrane, if the latter is located in a compartment above the suspension, where it is not wetted by the suspension. It is required that its gas permeability is high, as is the case for the already mentioned membranes of the type Celgard or Treopore. A small area of the second membrane is favorable in order to reduce a shading of the cell suspension, since the porous membranes are light-reflecting. Only the gas-permeability of the second membrane is crucial for the mass exchange across this membrane, when the membrane is not wetted with a liquid. If the second membrane were relatively small and covered by liquid film, a strong hindrance of the gaseous exchange would be achieved due to the low rate of gas absorption and de-sorption at a gas-liquid-interface. Although a continuous wetting of a hydrophobic membrane by splash contact with the suspension was not expected, the experience showed that it is favorable at high cell densities; to arrange the second membrane in a compartment of the reaction chamber, wherein it is protected from splashing with the cell suspension (
The research-PBR or its reaction chamber can be produced in disposable form using porous and hydrophobic membranes with the characteristics of the invention, for example the commercially available membranes described above, and preferably translucent plastics like polystyrene, or polycarbonate. A favorable embodiment of the research-PBR consists in the combination of a relatively large number of exchangeable reaction chambers with one large basis chamber. For the study of parallel batches this has the advantage, that all investigated cell suspension can be exposed to the same photon flux density, the same intensity of turbulent flow and the same conditions for CO2 entry. In this case it is favorable, when the basis chamber has no direct fluidic connection with the atmosphere.
Figures (schematic, not drawn to scale)
The limits of the geometric resistance factor of a research PBR according to the invention, F=A/Σ(QnLn−1), which is defined by the exposed surface area of the reaction chamber A and the channel parameters cross sectional area Q and L will be explained for the PBR schematically shown in
According to the duty of the invention the research-PBR should be suitable for high rates of photosynthetic turnover. Hence the channel dimensions are chosen in such a way that an increase in DB of 200 d−1 per m2 of the PBR surface exposed to the light, which slightly surpasses the highest value so far measured, does not induce a strong increase of the O2 concentration in the reaction chamber. The portion of carbon in the DB is similar to that in carbohydrate (CH2O). Hence at normal temperature (20-30° C.) the rate of O2 formation coupled to an increase in DB of 200 g m−2 d−1 is about 6.67 mol d−1, which corresponds to 167 l m−2 d−1 or 0.000193 cm3 cm−2 s−1. In a research PBR with an exposed surface of 1 dm−2 the rate of oxygen formation by one chamber would be 0.193 cm3 s−1 or 1.67 l per day. At the mentioned extremely high rate of photosynthesis the basis chamber should include a gas volume of at least 5 l in order to dilute the O2 volume formed at one day efficiently in its space. At the channel dimensions according to the invention the increase in the O2 concentration can be avoided by diffusive exchange of atmospheric N2 with the O2 formed in the reaction chamber. The stationary concentration difference □C between the space within the reaction chamber and the atmosphere is connected with the geometric resistance factor F, the diffusion coefficient D of O2 in air, and the rate of O2 formation per unit of the area exposed to light by the equation
ΔC=JFD−1
When a value for D representative for physiologic temperatures at atmospheric pressure (0.2 cm2 s−1) as well as values for J (0.000193 cm3 cm−2 s−1) and the geometry factor mentioned above (45.5 cm) is inserted into this equation, this results in a concentration difference ΔC amounting to 0.044 in the expression as molar ratio. This correlates with an enhancement of the O2 concentration in the reaction space by 4.4% (vol/vol) and a stationary O2 concentration within the reaction chamber of about 23.5%, when PBR is shaken in air. Hence, at the chosen channel dimensions (L=0.1 cm, Q1=0.2 cm2, Q2=0.1 cm, L2=1 cm) and an area of the PBR exposed to the light of 1 dm2, a physiologically relevant enrichment of oxygen within the reaction chamber does not occur even at an extremely high photoautotrophic turnover referred to the exposed surface.
The gas flow within the first (shorter) channel is larger than that in the second longer one. When the gas volume flow out of the PBR is 0.0193 cm3 s−1 (=100 cm2×0.000193 cm3 cm−2 s−1) as explained above, in the first channel (0.1 cm) it amounts to 0.0175 cm3 s−1 and in the second one (1 cm) it amounts to 0.00175 cm3 s−1. The velocity of viscous gas flow in the shorter channel would approach a value of 0.035 cm s−1, which is much below the velocity of O2 diffusion in this channel. The latter can be regarded as the permeability coefficient D/L of a 0.1 cm thick air layer for O2, which amounts to a value of about 2 cm s−1. Since the permeability coefficient surpasses the flow velocity about 57 times, the effect of the viscous gas flow on the diffusion exchange of N2 against O2 can be neglected. Due to the low value for the viscous flow resistance obtained in the longer channel (L=1, circular cross section) a nearly ideal pressure equilibration between the exchange space an the atmosphere would be achieved at the above mentioned extremely high value of the O2 formation rate in the reaction chamber (0.0192 cm3 s−1) even when the shorter channel would be closed. The pressure drop along the longer channel at this volume flux would be as small a about 0.32 mPa.
In a research PBR with an exposed surface amounting to 1 dm2 having a single channel with a cross sectional area Q of 0.05 cm2 and a length of 1 cm the factor F would be 2000 cm. At the extremely high rate of O2 formation per chamber (0.0193 cm3 s−1) the flow velocity in the channel would approach to 0.386 cm s−1. In this case the velocity of viscous gas flow would surpass the permeability coefficient of a layer of unstirred air with the thickness 1 cm for the exchange of N2 against O2 (0.2 cm s−1). Hence, N2 initially present within the air volume in the reaction chamber would be completely driven out of the reaction chamber by the viscous gas volume flow. Hence, a PBR with a resistance factor of 2000 cm can prevent oxidative stress only at rates of photosynthesis referred to exposed area that are fairly below the maximum so far measured.
Due to the limited saturating value of the water vapor concentration in air, the difference in the water vapor concentration between the inner space of the reaction chamber and the atmosphere cannot reach more than 30 mg l−1 or 4.2 percent (vol/vol) at a temperature of 30° C. The possible loss of water vapor also depends on the geometry factor F and is maximum at the lower limit for this factor according to the invention (F=20 cm). At this value of F and a water vapor concentration difference of 30 mg l−1 the calculated possible loss of water vapor amounts to about 1.2 g d−1, which represents 2.4% of the suspension volume at a thickness of the suspension layer of 5 mm.
Even lower values are obtained for the loss of CO2 through the channel(s), since the CO2 partial pressure in the basis chamber can be adjusted to a value that is fairly below that of water vapor. Further, when a weakly alkaline buffered medium is applied, wherein the absorbed CO2 is transformed to HCO3− before its consumption by the PMO, the CO2 partial pressure above the cell suspension remains very small, independent of the photosynthesis rate. In this case, the CO2 loss to the atmosphere is not technically relevant.
Research PBRs of the type shown in
The size of the surface area A exposed to the light was 25 cm2, the cross sectional area Q of the channel amounted to 0.063 cm2, and a channel length L of 0.2 cm was chosen. A polypropylene network served as gas permeable support layer; A 40 μm thick Treopore membrane (Type PDA) was applied as gas permeable membrane. The tight seal of the membrane on the basic board of the reaction chamber, the connection of both chamber and further modification of the culture vessels were carried out by gluing with transparent silicone. The sterilization of the reaction chamber was carried out by introduction of an 11% aqueous H2O2 solution (20 ml) into the vessel. After short panning and longer incubation (about 6 h) the major part of the oxidant solution was poured off and, after closure of the vessel with a silicon stopper, the residual liquid (1-2 ml) was allowed to evaporate across the gas-permeable membranes.
A culture medium was applied, which contained al macronutrient in a concentration that was sufficient for DB formation of 30 g l−1 referred to the suspension volume. The medium which was found to be suitable for the mentioned organism contained 150 mM NO3−, 100 mM K+, 10 mM HPO4−, 10 mM SO4; 10 mM Cl−, 10 mM Mg2+, 0.5 mM Fe2+, 0.5 mM EDTA, 0.5 μM Vitamin B12, 2 mM H3BO4, 100 μM Mn2+, 10 μM Zn2+, 6; MoO4, 0.2 μM Co2+ and 0.05 μM Cu2+. It was buffered with 100 mM NaHCO3. The culture medium was prepared by mixing at room temperature under a sterile flow box by adding one volume of a separately autoclaved 1M CaCl2 solution to 100 volumes of the autoclaved common solution of the other constituents. The reaction chamber contained 20 ml of this culture medium and the basis chamber was filled with 30 ml of a buffer obtained by mixing of 1 volume of a 3 M K2CO3 with 3 volumes of a 3 M KHCO3 solution.
The research PBR was fixed on 5 mm thick black-painted aluminum board on the shaking desk. There were holes within the board, into which the research PBRs could be inserted. The shaking desk was exposed to the light of two green house lamps (each 400 W), the light of which was filtered by 7 mm thick glass plate. The glass plate and the shaking desks were cooled by an air flow from aside. Using a board with adjustable height whereon the shaking desk was fixed the PFD could be adjusted to a value between 200 and 1200 μmol m−2 s−1. This device was located in a room with low relative humidity (<40%) of the air and an air temperature of 28° C. An efficient cooling of the exposed PBRs was ensured by the air flow. At high values of the PFD (>500 μmol m−2 s−1) the temperature of the reaction vessels was only slightly higher (less than 2° C.) than that of the air, while the temperature of the aluminum plate on which the basis boards of the PBRs were fixed, was higher (3 to 4° C. above the air temperature). This temperature difference between the basis chamber and the reaction chamber was sufficient to prevent a significant loss of water to the reaction chamber by osmotically mediated vapor distillation.
The PBRs were applied in the repeated batch mode, while they were shaken with 10 or 20 ml of the culture medium on a circular shaker adjustable at 200 to 400 rpm. The daily increase of the CDM was determined after strong dilution (1/100 to 1/20) with a spectral photometer by measuring the light attenuation at a wavelength of 750 nm using a calibration curve. Sampling during a growth cycle was carried after by removal of a small volume of the suspension (0.3 ml) through a closable and heat-sterilizable port, while the sampling at the start and the end of each cycle was carried out before dilution of the suspension, which was carried out under the sterile flow box. Inoculation was carried out with an initial CDB of about 0.3 g l−1. Already after one day there was stated a CDB of 2 to 3 g l−1. The increase of the CDB on the following days depended on the PFD in a nearly linear manner in the PFD range between 400 and 1200 μmol m−2 s−1.
To realize the repeated batch culture regime the cell suspension was diluted with the fresh nutrient solution in two day cycles. The suitable dilution rate was calculated and defined after measuring the CDB to a value ensuring that the CDB after dilution reached approximately 2 g l−1 as the initial value of the next cycle.
At a PFD of 850 μmol m−2 s−1 the CDB increased from about 2 g l−1 to a value amounting to 25 to 27 g l−1 within 48 h. This corresponds to an absolute value of the daily increase in the DB of more than 0.2 g per reaction chamber or of more than 40 g per m2 of the area exposed to light. The increase in the DB per reaction chamber was largely independent of the thickness of the cell suspension layer (4 or 8 mm), from which it may concluded that PFD was the limiting factor. Probably even higher photosynthetic turnover rates could be obtained at higher values of the PFD. At a volume of 20 ml of the cell suspension (thickness of the unshaken suspension 8 mm) the DB reached 12 to 15 g l−1 after the second day. At a suspension layer thickness of 4 mm the daily increase of the DB, referred to volume, was 12 to 13 g l−1.
Using the measuring device illustrated in
Two research PBRs according to
The suspension volume amounted to 20 ml (layer thickness 8 mm). The channel of the research PBR shown at the right side was more narrow and longer than at the one shown in the PBR shown at the left side. The duration of the culture (dilution) cycle was two days. In the PBR shown at the right side the resistance factor of diffusive gaseous exchange per area exposed to the light was smaller (F=79.4 cm) than in that shown at the left side (F=794 cm). Here the increase in DB at the second day was slightly larger than at first day and amounted to more than 40 g m−2 d−1. In the chamber variant with the larger resistance of diffusive gaseous exchange the increase in the DB was not different from that in the parallel variant at the first culture day. At the second culture day, however, it was markedly smaller (25 to 35 g m−2 d−1) than in the parallel variant. The result was found without exception in 5 following cycles. When the F value of the chamber variant shown left was reduced from 794 cm to 79.4 cm by shortening the channel from 1 cm to 0.1 cm, in this variant the increase in DB during the second day also surpassed the value of the first day and a significant difference between both variants could not be stated anymore. It can be deduced from the equation ΔC=F J D−1 (see first execution example) that the O2 concentration in the reaction chamber can rise above the value of the outer atmosphere only a little (by 1.5% vol/vol), when F=79.4 at a daily increase in dry weight referred to the exposed area of 40 g per m2 (J=38.6.×10−4 cm3 cm−2 s−1). The equation also shows that steady state value for the O2 concentration must be markedly higher (ca. 35% vol/vol) than that of air at the same rate of photosynthetic turnover at an F value of 794 cm. The results show that the O2 concentration in the chamber with the larger F value reached a growth-inhibiting value only at the second day. This can be explained by the fact that at each dilution of the cell suspension there was an exchange of the relatively large gas volume in both chambers of the research PBR with the atmosphere.
The experimental device shown in
At the higher frequencies of shaking the mean rate of CO2 absorption from the membrane area amounted to 34.2 μmol cm2 s−1. This would enable a daily rate of photosynthesis according to the consumption of 8.2 mol CO2 per m2 d−1 or the formation of 246 g CH2O m−2 d−1, which surpasses the highest rates of photosynthesis per unit area exposed to light so far known. Even higher rates of CO2 absorption were obtained, when a 1 M KOH was shaken in the experimental device. This was expected, since the reaction of the dissolved CO2 to bicarbonate and carbonate is extremely rapid at the high concentration of OH− ions in this solution and can prevent the saturation of the liquid at the interface with CO2 (Edsall 1969)
| Number | Date | Country | Kind |
|---|---|---|---|
| 102013015969.5 | Sep 2013 | DE | national |
