Customization of Aspergillus niger Morphology Through Addition of Talc Micro Particles

1. Reactor Setup and Start of Cultivation

4 bioreactor cultivations in total are conducted.

1. Use a 3 L stirred tank bioreactor with a working volume of 2.2 L for the cultivation of A. niger SKAn1015.
2. Pour 72.6 g glucose monohydrate into the reactor and fill it up with 1.9 L deionized water.
3. Install the reactor equipment such as 3 baffles, a two six-bladed disk turbine impeller, a pH electrode, a gas inlet with air filter, a cooling finger, an exhaust air cooler with air filter, an immersion tube for sterile sampling with air filter and inlet hoses for medium, inoculum, acid and base.
4. Autoclave the reactor at 121 °C for 20 min.
5. Connect the reactor with the acid-base reservoir (2 M HCl, 2 M NaOH) and the corresponding pumps and set up a pH-value of 5.0 ± 0.05 with the pH control unit.
6. Link the reactor with the cooling-water system and put the heating jacket around the reactor vessel.
7. Install the temperature sensor with corresponding control unit and set up a temperature of 37 ± 0.1 °C at the temperature control unit.
8. Fit the agitation motor atop of the reactor and bring it into service with an agitation speed of 200 min^-1.
9. Add the sterile minimal growth medium¹¹ trough one of the sterile inlet hoses (250 mL). For medium preparation all components were autoclaved at 121 °C for 20 min and mixed together. For three cultivations the components include talc powder (3MgO•4SiO₂•H₂O) in the concentrations of 1 g/L (reactor 2), 3 g/L (reactor 3) and 10 g/L (reactor 4). Prior to use, re-suspend the micro particles in 50 mM sodium acetate buffer (pH 6.5) and add it to the sterile medium. In control cultures (without particles) replace the micro particle suspension by 50 mM sodium acetate buffer (pH 6.5).
10. Add the spore suspension (inoculum) as prepared in Wucherpfennig et. al (2011)¹¹ trough one of the sterile inlet hoses (50 mL) so that the concentration of spores amounts to 1X10⁶ mL^-1. The inoculation marks the start of cultivation (h = 0 h).
11. Start the aeration with a rate of 1.0 L min^-1.

2. Sterile Sampling after 24, 48 and 72 h of Cultivation

1. Take 50 mL of sterile culture broth into a flacon tube.
2. Use sample for determination of biomass dry weight, β-fructofuranosidase activity and microscopic analysis.

3. Determination of the Biomass Dry Weight after 24, 48 and 72 h of Cultivation

1. Biomass samples are to be taken at least in duplicate.
2. Weight a cellulose filter with a micro scales after drying in the desiccator and place the filter in a Büchner funnel with connected water-jet vacuum pump.
3. Filter a defined sample volume (e. g. 10 mL) and rinse the filter with 10 mL deionized water to remove medium compounds from the biomass.
4. Wrinkle the filter once in the middle, place it in a glass Petri dish and put it into a compartment dryer until weight constancy (at least 24 h).
5. Cool the filter in a desiccator and measure the weight.
6. Calculate the biomass dry weight as the difference between the weight of the filter with and without dried biomass divided by the used sample volume.

4. Determination of the Extracellular Enzymatic Activity of β-fructofuranosidase by GOD/POD-essay after 24, 48 and 72 h of Cultivation

Store the samples on ice constantly while working with them.

1. Filter 1.5 mL culture suspension trough a cellulose acetate filter by pressing the culture suspension with a syringe through the filter into a reaction tube. Store the reaction tube at -20 °C until usage.
2. For the reaction mixture use 20 μL sample and add 200 μL of 1.65 M sucrose dissolved in 0.05 M phosphate buffer (pH 5.4) to initiate the reaction from sucrose to glucose. Cary out the reaction at least in duplicate.
3. Incubate the reaction mixture at 40 °C for 20 min in a heating block. Stop the reaction by incubating at 95 °C for 10 min in a heating block. Cool the reaction mixture by storing it on ice and spin down the condensed water by centrifuge at 13.000 g for 10 min at 4 °C.
4. To account the pH and temperature dependent cleavage of sucrose to glucose, carry out a blank value by using 20 μL deionized water instead of 20 μL sample.
5. To account for residual glucose in the culture broth, carry out a negative control for each sample. To that end use 20 μL of the sample and inactivate β-fructofuranosidase by heating at 95 °C for 10 min prior to add the sucrose and incubate as described in step 4.3.
6. Dilute the samples such that the following measured adsorption is in the calibrated value range.
7. Carry out all enzymatic assays in triplicate. Apply 2 μL diluted sample in a micro titer plate well. Apply a standard range for calibration on the micro titer plate by each using 2 μL of ten glucose solutions with ten different know concentrations (from 1 mM to 15 mM) instead of 2 μL sample. For zero point calibration use 2 μL deionized water instead of 2 μL sample.
8. Add 200 μL of the reagent solution to each well by using a multi pipette.
9. Incubate the mixture for 10 min at room temperature.
10. Store the micro titer plate at 6 °C until measurement (a few hours at most).
11. Measure the absorption at 450 nm using a 96-well Sunrise micro plate reader and the Magellan data retrieval software. Set the mixing time up to 5 sec. and the rest period up to 1 sec.
12. Open the result chart with a spreadsheet and construct a calibration line by using the standard range:
    glucose concentration = a X absorption + b
    
13. Calculate the activity:
    activity = (absorption X dilution factor-blank value ) X a+b
    
14. Figure out the β-fructofuranosidase activity by calculating the difference between the activities of the sample and the appropriate negative control.
15. Calculate the specific productivity for following use by taking into account biomass dry weight and β-fructofuranosidase activity ¹¹.

5. Microscopy and Automated Image Analysis after 72 h of Cultivation

1. Place around 3 mL culture suspension in a plastic Petri dish and dilute them with physiological sodium chloride solution until the morphological structures are separated.
2. Situate the Petri dish under a microscope, which features an integrated or connected camera. Acquire and save about 100 images (Figure 2) of morphological structures per sample. Pay attention that on each image at least one object is completely pictured.
3. Open all images of the same sample with the image processing program ImageJ¹². Convert the images to black and white by using the process tool “Make Binary” (Figure 2). For applying the command to the whole series of images use a macro code as follows.
   run(,,Make Binary”)
   
4. Open the processed binary images with ImageJ again. Calculate the shape factors Feret’s diameter, projected area, perimeter, circularity, aspect ratio, roundness und solidity for every image with the analyze tool “Set Measurement”. For applying the command to a series of images use a macro code as follows.
   run(“8-bit”);
   run(“Make Binary”);
   run(“Set Scale…”, “distance=X known=1000 pixel=1 unit=μm global”);
   run(“Set Measurements…”, “area perimeter shape feret’s limit display redirect=None decimal=3”);
   run(“Analyze Particles…”, “size=10000-Infinity circularity=0.00-1.00 show=Outlines display”);
   Determine X as the number of pixels which correlates to 1000 μm by constructing a straight line across a scale bar. Correlate the number of pixels of the straight line with the length of the scale bar in μm.
5. Open the result chart containing shape factor values for each image with a spreadsheet. Calculate a Morphology number as follows for each image.
   
6. Calculate mean value and standard deviation for the Morphology number taking into account all images of one sample.
7. Use a graphing and data analysis program for graphical correlation of the Morphology number with the specific productivity and determine the mathematical relation by mathematical regression.

6. Representative Results

Through addition of talc micro particles A. niger SKAn 1015 morphology is changed from a true pellet morphology to a dispersed or even mycelial morphology. Whereas pellet morphology is exhibited at standard conditions a mycelial morphology is created by supplementation of medium with 10 g/L of talc micro particles (Figure 4.). Concurrently the activity of β-fructofuranosidase increases around 3 fold ^3-5. A supplementation of 1 or 3 g/L of talc powder leads to a dispersed morphology, with a doubled fructofuranosidase activity (Figure 4.).

The micro particle dependent morphology can be comprehensively described by the Morphology number which can be calculated using parameters determined by automatic image analysis. Perfectly round and smooth pellets will in microscopic images appear as perfect circles. For such particles the Morphology number has a value of 1. The smallest fragment of mycelial morphology can be simplified as a one-dimensional line yielding a Morphology number of 0. All intermediate morphological forms like elongated irregular pellets or clumps will therefore have values between 0 and 1. Fairly large particles will result in a high, fungal particles with a large surface or elongated particles, in a rather low Morphology number ¹¹.

At standard conditions the morphology in reactor 1 exhibits a Morphology number around 0.8. The morphology in reactor 4 with 10 g/L talc powder features a Mn around 0.1. The Morphology number for reactors 2 and 3, with talc powder concentrations of 1 and 3 g/L, lies between these extremes, demonstrating a dispersed morphology. Since micro particle dependent morphology is closely related with the β-fructofuranosidase productivity, a mathematical correlation of Morphology number and productivity similar to Figure 5 is obtained.

Figure 1. Overall scheme of the experimental design and the analytic procedure. A. niger is cultivated (with or without micro particles) in an 3 L stirred tank bioreactor for 72 h. After 24, 48 and 72 h a sample is taken for determination of biomass dry weight and β-fructofuranosidase activity, which again are used for calculation of the specific productivity. After 48 h the fungal morphology is examined by microscope and characterized by digital image analysis. Relevant parameters of image analysis are combined to a Morphology number, which is mathematical correlated with the specific productivity.

Figure 2. Steps of image processing for microscopic-generated images of morphological structures from A. niger. Step 1: image acquisition by microscope. Step 2: image improvement if necessary. Step 3: image binarization, black-and-white (binary) image generated in ImageJ. Step 4: the binary image is processed by and unwanted object are cleared. Step 5: morphological analysis is conducted with the “Analyze particles” function of the open source program ImageJ.

Figure 3. Different morphological forms of A. niger dependent on the concentration of added micro particles. With increasing concentration of micro particles added the pellet size can be precisely decreased down to small core-shell pellets, small flocks and even freely dispersed mycelium. Morphology engineering of Aspergillus niger SKAn1015 by micro particle supplementation in submerged culture. Without microparticles (A), 10 mg/L (B), 0.1 g/L (C), 0.2 g/L (D), 0.3 g/L (E), 0.6 g/L (F), 1.0 g/L (G), 1.5 g/L (H), 2.0 g/L (I), 2.5 g/L (J), 3.0 g/L (K), 3.5 g/L (L), 4.0 g/L (M), 4.5 g/L (N), 5.0 g/L (O), 10 g/L (P), 15 g/L (Q), 20 g/L (R), 30 g/L (S) and 40-50 g/L (T). Images were taken by light microscopy after 72 h of cultivation.

Figure 4. Fructofuranosidase activity in dependence of talc micro particle concentration 1 g/L (reactor 2), 3 g/L (reactor 3) and 10 g/L (reactor 4). Reactor 1 is not supplemented with micro particles; here the cultivation is conducted under standard conditions.

Figure 5. Representative good correlation (R² = 0.91) of the Morphology number and the specific productivity. The Morphology number is plotted (abscissa) against the specific productivity (ordinate). Nonlinear regression yields the exponential correlation.