- Original article
- Open Access
Tailoring fungal morphology of Aspergillus niger MYA 135 by altering the hyphal morphology and the conidia adhesion capacity: biotechnological applications
© Colin et al.; licensee Springer. 2013
Received: 26 February 2013
Accepted: 10 May 2013
Published: 20 May 2013
Current problems of filamentous fungi fermentations and their further successful developments as microbial cell factories are dependent on control fungal morphology. In this connection, this work explored new experimental procedures in order to quantitatively check the potential of some culture conditions to induce a determined fungal morphology by altering both hyphal morphology and conidia adhesion capacity. The capacity of environmental conditions to modify hyphal morphology was evaluated by examining the influence of some culture conditions on the cell wall lytic potential of Aspergillus niger MYA 135. The relative value of the cell wall lytic potential was determined by measuring a cell wall lytic enzyme activity such as the mycelium-bound β-N-acetyl-D-glucosaminidase (Mb-NAGase). On the other hand, the quantitative value of conidia adhesion was considered as an index of its aggregation capacity. Concerning microscopic morphology, a highly negative correlation between the hyphal growth unit length (lHGU) and the specific Mb-NAGase activity was found (r = -0.915, P < 0.001). In fact, the environment was able to induce highly branched mycelia only under those culture conditions compatible with specific Mb-NAGase values equal to or higher than 190 U gdry.wt -1. Concerning macroscopic morphology, a low conidia adhesion capacity was followed by a dispersed mycelial growth. In fact, this study showed that conidia adhesion units per ml equal to or higher than 0.50 were necessary to afford pellets formation. In addition, it was also observed that once the pellet was formed the lHGU had an important influence on its final diameter. Finally, the biotechnological significance of such results was discussed as well.
Filamentous fungi have been extensively used in biotechnological processes as cell factories due to the metabolic versatility of this group of microorganisms. They are known for their capacity to secrete high levels of enzymes, antibiotics, vitamins, polysaccharides and organic acids (Meyer 2008). Mycelia are also suitable for application in treatment of dye and textile wastewater (Romero et al. 2006; Blánquez et al. 2007). However, one particular difficulty with this kind of microorganisms centers on their morphological form. The observed hyphal morphology can vary from linear filaments to highly branched structures, while growth morphologies in submerged culture varying from compact pellets to dispersed mycelia. Both microscopic and macroscopic morphology affects the broth rheology and in this turn may affect product yield (Grimm et al. 2005). A number of culture conditions have been identified as having the potential to bring about substantial change in fungal morphology. It is well documented that morphology is influenced by medium composition, pH, temperature, additives (surfactants, chelators, polymers), inoculum and dissolved oxygen and carbon dioxide (Papagianni 2004). However, it has to be mentioned that much of the published work is descriptive, with relatively little attempt made to obtain quantitative work related to the control of fungal behavior in liquid culture. Thus, understanding the growth and morphological development during submerged cultures is therefore, an important part in studies of the fermentation processes of filamentous fungi (Pera et al. 2008 2010).
Dispersed mycelial growth is preferred for many processes, but increases the viscosity of the medium and can wrap around impellers, cause blockages and spread into sampling and overflow lines (Prosser and Tough 1991). As a valuable strategy to overcome such obstacles, several authors have reported the use of immobilized mycelium (Papagianni and Mattey 2004; Mizunuma et al. 2007). Alternatively, growing the organism in the pelleted form also removes these problems and facilitates downstream processing by simplifying solid–liquid separation procedures. However, big pellets may often result in the diffusional limitation of oxygen and other nutrients. These limitations can finally induce autolytic processes within the inner part of those pellets. Therefore, the ability to obtain and control a certain pellet size would be a key to increase the mycelium productivity. As an interesting approach in this direction, a low hyphal growth unit length (lHGU) has been associated with the formation of clumps smaller than those formed at a high lHGU (Bocking et al. 1999). Moreover, although the exact process of pellets formation is not fully understood, the initial step of some pelletization events is suggested to involve conidia aggregation (Prosser and Tough 1991). In this connection, quantitative values of conidia adhesiveness could be valuable information.
On the other hand, the cell wall is a complex and dynamic structure and site of diverse enzyme activities. The balance between wall synthesis and wall lysis is critical, since wall synthesis in the absence of lysis can cause excessive wall thickening and possible growth arrest, whilst lysis in the absence of synthesis would produce bursting of the cell. Thus, within permissible limits, the net balance between wall synthesis and wall lysis will exert a marked influence on cell growth and hyphal morphology (Grove 1978). In this connection, the activity β-N-Acetyl-D-glucosaminidase (EC 22.214.171.124) (NAGase) from Aspergillus niger MYA 135 was chosen as a relative marker of the wall lytic potential (Bartnicki-García and Lippman 1972). This enzyme was isolated, purified and characterized, and dose–response experiments of those effectors that influence hyphal morphology of A. niger MYA 135 were also conducted (Pera et al. 1997). In this work, the mycelium-bound NAGase (Mb-NAGase) activity was used as a biochemical marker of the wall lytic potential to quantitatively check the capacity of some culture conditions to induce a desired hyphal morphology. To this end, the influence of environmental conditions on both hyphal morphology and cell wall weakness was firstly evaluated. Later, a basic mineral medium at different temperatures as well as an aliquot of several culture media was exposed to a Mb-NAGase activity, and then the specific activity was calculated and related to the resulting hyphal morphology obtained under each assayed condition after 72 h of cultivation.
Thus, a quantitative assessment of hyphal morphology and conidia adhesion capacity of A. niger MYA 135 under different environmental conditions, and how those parameters affect the macroscopic morphology were the main goals of this study.
Materials and methods
Microorganisms and culture conditions
Aspergillus niger ATCC MYA 135, formerly A. niger 419 from our own culture collection, was used throughout this work. To produce conidia, the microorganism was grown on potato dextrose agar (PDA) for 10 to 20 days at 30°C. The PDA medium contained (g l-1): infusion from 300 g potatoes; dextrose, 10.0; agar-agar, 20.0. The culture flasks were incubated to a final concentration of about 105 conidia ml-1. The basic culture medium (BM) contained (g l-1): sucrose, 10; KH2PO4, 1; NH4NO3, 2; MgSO4, 0.2; CuSO4, 0.06. All parameters measured from mycelial pellets grown in BM at 30°C and initial pH 5 were considered as a reference, because it was possible to detect significant changes of them above or below to these determined under the reference conditions. The cultivations were conducted in 50 or 500 ml conical flasks, containing 10 or 100 ml of BM, respectively, on an orbital shaker at 200 rpm during 72 h. The effect of modification in the environmental conditions on biomass production, fungal morphology and conidia adhesion was tested by changing either the temperature of incubation or the initial pH of the medium as well as by the addition of either 0.5 g l-1 CaCl2 or 1 g l-1 FeCl3 to the BM. At the end of the incubation period the biomass was determined by drying washed mycelia at 105°C to constant mass.
Microscopic and macroscopic observations
Cell morphology was analyzed with Nomarski differential interference contrast (DIC) optics, utilizing a Nikon ECLIPSE 80i microscope with a 100× 1.3 NA objective.
Morphological parameters such as pellet diameter, hyphal growth unit length (lHGU) and hyphal diameter as well as the numbers of pellets per liter were determined after 72 h of incubation by using the Nikon EclipseNet software package version 1.20.
For measurement hyphal lengths fragments, mycelia were collected, immediately suspended in distilled water and disintegrated with a dissection needle, until microscopic examination showed that the fungal hyphae were separated from each other. The lHGU was calculated by dividing the total length for each organism by the number of tips. For each sample, an appropriate number of mycelial elements was analyzed (n ≥ 20), and the mean values calculated. Lengths were obtained by skeletonizing hyphal trees and using a pre-set calibration (in μm). Samples were analyzed at a total magnification of 400 ×. In addition, the arithmetic values of all morphological parameters passed the Anderson-Darling normality test.
The final macroscopic morphology (pellets or dispersed mycelium) obtained under each culture condition tested was also evaluated.
Production of a wall lytic potential biomarker
Mycelial pellets produced in BM at initial pH 5, during 72 h, at 30°C were directly used as a source of Mb-NAGase activity.
Determination of Mb-NAGase activity as a wall lytic potential biomarker
The response of the wall lytic potential biomarker (Mb-NAGase activity) towards different in vitro environmental conditions was evaluated in a reaction system as follows: to 500 μl of each culture medium without inoculum, about 0.010 g of wet mycelium (Mb-NAGase activity), and 50 μl of 3.6 mM p-nitrophenyl-N-acetyl-β-D-glucosaminide were added. The mixture was shaken at 200 rpm with magnetic bars at the corresponding temperature and, after addition of 1000 μl of 0.25 M Na2CO3 to stop the reaction, was centrifuged at 5000 g for 10 min. The optical density at 405 nm was measured in the supernatant, and enzyme activity was then calculated and related to biomass dry weight. A calibration curve was generated with wet and dry mycelia (R2 = 0.973).
Note that the aliquot of each medium was taken before inoculation. This is because conidia also have an ungerminated conidia-bound NAGase activity (data not shown).
One unit of enzyme activity was defined as the amount of biocatalyst that released 1 μmol of p-nitrophenol per minute.
Determination of conidia adhesion
The adhesion capacity of A. niger conidia was assayed using 96-wells polystyrene microtiter plates as a substrate. According to the experimental protocols, 6 ml of culture samples were periodically withdrawn at 0, 2, 4 and 6 h of cultivation, centrifuged 10 min at 12,000 rpm, resuspended in 600 μl by using their own medium and dispensed in three wells. Plates were incubated at the same temperature at which the fungus was developed on an orbital shaker at 200 rpm, and then the medium containing most of the unbound conidia was removed by inverting the plate onto an adsorbent pad. Conidia adhesion was quantified with the protein stain sulforhodamine B (SRB). Conidia were fixed by incubation at 4°C for 1 h after the addition of 200 μl of 10% (v/v) trichloroacetic acid. The trichloroacetic acid was removed, the wells were washed five times with water, and the plates were allowed to dry in a chemical hood. Conidia were stained for 30 min at room temperature by the addition of 200 μl of a 0.4% (w/v) solution of SRB in 175 mM acetic acid to each well. The stain was removed by aspiration, and the plates were washed four times with 175 mM acetic acid. Then, the plates were dried by using a microwave oven for 15 min. The bound dye was extracted by adding 200 μl of 10 mM unbuffered Tris base (pH 10.1) to each well and shaking the plates for 10 min at 250 rpm. The resulting pink color in the wells was quantified by measuring the absorbance at 570 nm (Slawecki et al. 2002). The adhesion unit (U) was defined as the amount of adherent substance that produces an increase in absorbance at 570 nm of 0.01 per min. The conidia adhesion was expressed as U per ml of culture. For each environmental condition tested, a minimum of nine replications were made.
Influence of conidia-aging on adhesion
The influence of conidia-aging on adhesion to polystryrene wells was firstly tested after 3 h of incubation at 30°C by using ungerminated conidia from 2 to 40-day-old suspended in BM at initial pH 5. Secondly, adhesion units per ml of either 10 or 30-day-old conidia were also determined during the first hours of cultivation (0, 2, 4 and 6 h).
Influence of azide on conidia adhesion
Conidia were suspended in BM, in BM supplemented with 2 mM azide, in water as well as in water supplemented with 2 mM azide, and they were incubated at 30°C. Culture samples were periodically withdrawn and the adhesion units per ml detected during the first hours of cultivation were determined as described above.
Statistical analyses were performed using the Infostat (version 2004; Grupo InfoSat, FCA, Universidad Nacional de Córdoba, Córdoba, Argentina) and the Minitab (version 14; Minitab Inc) softwares for windows. Statistical significance values of the means were evaluated using a one-way analysis of variance. Subsequent comparisons were performed using Tukey’s post-hoc test. Results were presented as the mean ± SD. Differences were accepted as significant when P < 0.05. In addition, the Durbin-Watson test was used to detect the presence of autocorrelation in the residuals from a regression analysis.
The huge efforts in the characterization of fungal morphology show an evident connection between the operating environment of the bioprocess and the morphology and metabolic properties of individual cells (Krull et al. 2013). In this work, new experimental procedures were explored in order to quantitatively check the potential of some culture conditions to induce a determined fungal morphology by altering both hyphal morphology and conidia adhesion capacity.
Influence of environmental conditions on biomass production and fungal morphology
Compared to the mycelial yield obtained under reference culture conditions (BM at 30°C and initial pH 5), in BM supplemented with 0.5 g l-1 CaCl2 or 1 g l-1 FeCl3 the biomass production was increased by 45 and 49%, respectively (Figure 2). However, their cellular morphologies were completely different. In the presence of CaCl2 numerous bulbous cells containing a large spherical vacuole and intercalary compartments abnormally short, appearing “barrel-shaped” in some cases, were observed (Figure 3D). Whereas, cells obtained in the presence of FeCl3 exhibited septa at a sufficient distance from one another, tubular vacuoles and, punctuated structures similar to those observed in hyphae grown at 25°C (Figure 3E).
Bulbous cells obtained in the presence of 0.5 g l-1 of CaCl2 appear to be bigger than those developed at 37°C. This fact was indicated by their 95% confidence intervals for the mean main diameter, that range from 15.24 and 12.59 μm to 17.81 and 14.44 μm, respectively, as well as by the relative position of the peaks for the fitted normal distribution (data not shown). In addition, both phenotypes were restored in a high osmolarity medium, suggesting the presence of a weakened cell wall (Figure 3F and 3G). No bulbous cells were observed in a medium supplemented with 1.5 M NaCl.
It is also important to mention that the morphological characteristics of growth were already apparent after about 24 h of incubation (data not shown).
On the other hand, during the early stages of the pelleted form of growth, conidia from A. niger MYA 135 produced a presumptively adhesive extracellular compound, probably an exopolysaccharide, visible under the optical microscope (Figure 3H). This amorphous material was not observed when the microorganism grew mainly as dispersed mycelia. Eventually, conidia could form small conglomerates, which grew laxly, along with hyphae originated from single, i.e., non associated conidia, apparently free of extracellular compound (data not shown).
Effect of sodium azide on A. niger MYA 135 conidia adhesion
Time course of adhesion capacity (U ml -1) ± SD
MB (basic medium)
0.89 ± 0.03
1.84 ± 0.04
2.10 ± 0.08
2.52 ± 0.16
MB + 2 mM NaN3
0.55 ± 0.03
0.54 ± 0.02
0.54 ± 0.02
0.57 ± 0.05
H2Od + 2 mM NaN3
Effect of environmental conditions on pellet diameter and pellets number in cultures of A. niger MYA 135
Pellet diameter (mm)
Pellets l -1(x10 3)
0.28 ± 0.06 b
275 ± 3 f
1.12 ± 0.11 d
60 ± 3 d
1.31 ± 0.30 e
55 ± 3 c, d
1.44 ± 0.32 f
45 ± 3 b
2.51 ± 0.36 g
22 ± 2 a
2.75 ± 0.32 h
19 ± 2 a
1.35 ± 0.11 e, f
41 ± 4 b, c
1.31 ± 0.30 e
55 ± 3 c, d
0.46 ± 0.09 c
249 ± 6 e
CaCl2 (0.5 g |-1)
0.14 ± 0.04 a
328 ± 8 g
FeCl3 (1.0 g |-1)
Influence of environmental conditions on a mycelium-bound β-N-acetyl-D-glucosaminidase activity and its relationship with hyphal morphology
The cell wall is essential for maintaining the osmotic balance and the shape of the cell. So, considering that a weakness in the cell wall was observed under determined culture conditions (Figure 3F and 3G) and that the site of new branch must be weakened to permit the formation of a new apex, the response of a wall lytic enzyme such as the mycelium-bound β-N-Acetyl-D-glucosaminidase (Mb-NAGase) activity was evaluated as a relative marker of the wall lytic potential.
In order to quantitatively examine how some environmental conditions affect the microscopic morphology, the lHGU and the average hyphal diameter of the mycelium obtained in each batch after 72 h of cultivation were determined. In this analysis, the bulbous cell diameters were not included. The lHGU and the average hyphal diameter for the A. niger MYA 135 growing under reference conditions (BM at 30°C and initial pH 5) were 108 ± 14 μm and 3.5 ± 0.2 μm, respectively. These values were significantly modified by the pH of the medium, the presence of metal ions as well as by the temperature of incubation (Figure 5B and 5C).
Influence of environmental conditions on conidia adhesion and its relationship with pellets formation
Because conidia of A. niger MYA 135 are of the coagulative type, quantitative values of conidia adhesiveness and its relationship with pellets formation could be a valuable information.
The influence of Ca++ on the extent of conidia adhesion was interesting. Although in the presence of 0.5 g l-1 CaCl2 the conidia adhesion follows the same pattern to that observed under reference conditions (BM at 30°C and initial pH 5), the adhesion capacity was reduced by about 26% (Figure 7B). It was also observed a significantly reduction in mean pellet diameter and an increase in the average number of pellets per liter (Table 2).
Finally, the temperature of incubation did not appear to significantly affect conidia adhesion after 2 h of cultivation (Figure 7B). However, at 37°C, a significant reduction of pellet diameter as well as a significant increase of the number of pellets per liter was observed (Table 2). As it will be discussed below, these effects could be explained by the increase of the mycelia branching degree (Figure 5B).
Simple linear regression between pellet diameters versus conidia adhesion using A. niger MYA 135
S = 0.634256
R2 = 52.0%
R2 (adj) = 46.0%
DW = 1.59708
Multiple linear regression between pellet diameters versus conidia adhesion and hyphal growth unit length using A. niger MYA 135
S = 0.407917
R2 = 82.6%
R2 (adj) = 77.7%
DW = 1.87488
Fungal morphology is often a bottleneck of productivity in several industrial processes; and in many cases, the problems generated by fungal development are solved based on operator experience. Thus, its control is a challenge not only in basic mycology but also in fungal biotechnology. Many studies have investigated the cellular and molecular components involved in shaping of fungal cell, but the mechanisms that govern and regulate polarized growth are still only partially understood (Rittenour et al. 2009; Amicucci et al. 2011). Concerning fungal development, it has been stated that for the production of some industrial metabolites specific growth morphology is necessary. In some processes, dispersed mycelium is required as in the production of penicillin from Penicillium chrysogenum and in the synthesis of pectinases by Aspergillus niger. While, pelleted growth is preferred for the production of citric and itaconic acids using Aspergillus niger and Aspergillus terreous, respectively (Žnidaršič and Pavko 2001; Papagianni 2004). Thus, since there is an abundance of literature on the optimal fungal morphology for a given bioprocess (Wucherpfennig et al. 2011), it was an important objective of this work to link fungal growth to quantitative determinations of both hyphal morphology and conidia adhesion capacity.
Concerning macroscopic morphology, the production of an adhesive compound could be one of the reasons for the initial aggregation of conidia to form pellet nuclei, enabling the further formation of pellets by the subsequent aggregation of small clamps of germinated conidia (Prosser and Tough 1991). In this connection, although several lines of evidence suggest that an extracellular compound secretion is involved in the conidia aggregation of many fungal species (Zelinger et al. 2006; Fontaine et al. 2010), Deyesen and Nielsen (2003) also explain this process as a result of hydrophobic and electrostatic interactions by using Aspergillus nidulans as a model. Interestingly, when A. niger MYA 135 grew mainly as dispersed mycelia the presence of an extracellular compound, if any, was only detected with electron microscope (data not shown). In addition, the production of an emulsifier activity was significantly increased (p < 0.05) under environmental conditions that support dispersed mycelial growth (Colin et al. 2010a). Similarly, Prosser and Tough (1991) reported that the addition of nonionic surfactants, e.g., Span, to shake-flask cultures of A. niger also decreases spore aggregation thus allowing for dispersed growth. These observations encourage us to quantify the conidia adhesion capacity under different environmental conditions.
Firstly, it is important to note that the age of conidia significantly affected the adhesive competence of ungerminated conidia from A. niger ( MYA 135. Like us, Amiri et al. 2005) reported on a lower adhesion capacity to polystyrene of Penicillium expansum 40 day-old conidia, compared to the 15 day-old conidia. According to Smith et al. (1998), these results could be compatible with a decrease of the surface hydrophobicity of conidia ageing. However, these authors did not indicate what happens with conidia younger than 10 day-old.
Additionally, the capacity of ungerminated conidia from A. niger MYA 135 to adhere was affected by their exposure to a respiration inhibitor such as azide. This result suggested that the metabolism has a major role in the adhesion capacity of these conidia. However, it should be pointed out that conidia from A. niger MYA 135 could also have a preformed adhesive material (Schumacher et al. 2008) that is functional in BM at initial pH 5 and not in water. In contrast, the conidia adhesiveness of other filamentous fungi such as Stagonospora nodorum (Newey et al. 2007) and Botrytis cinerea (Doss et al. 1993) is not affected by this respiration inhibitor, showing that in these cases the metabolism is not required.
Interestingly, during the early stages of A. niger MYA 135 growth four differential responses concerning the conidia adhesion capacity over the time under different environmental conditions were observed such as no capacity to adhere, an initial adhesion capacity that is not significantly modified over the time, a conidia adhesion capacity that is gradually increased over the time and a conidia adhesiveness that is drastically increased over the time. In addition, this study also showed that conidia adhesion units per ml equal to or higher than 0.50 were necessary to afford pellets formation.
The pH value of the culture medium is a very important factor for several fungi to form pellets. In agreement with reports on A. niger growth morphology (Papagianni 2004), A. niger MYA 135 pellets formation decreased with increasing initial acidification of the culture medium. Besides, as it was shown in this work, the conidia adhesion capacity appears to be pH dependent as well.
Fungal morphology has been established as one of the key bioprocess parameters. In this context, the presence of metal ions in submerged fermentations significantly changes the macroscopic morphology and the metabolite production of A. niger MYA 135. Under citric acid culture conditions, the presence of 0.5 g l-1 CaCl2 in the fermentation medium favors pellets formation of about 1 mm in diameter. Besides, the specific citric acid production (g citric acid per g biomass dry mass) increases by 40%, while the volumetric productivity (g citric acid per l per h) and the yield (g citric acid per g initial sucrose) are doubled (Pera and Callieri 1997). On the other hand, the dispersed mycelium obtained in the presence of 1 g l-1 FeCl3 is preferred for the production of both a bioemulsifier (Colin et al. 2010a) and a mycelium-bound transesterification lipase activity (Colin et al. 2011).
Concerning microscopic morphology, this work explored a new experimental procedure in order to quantitatively check the potential of some culture conditions to induce a determined hyphal morphology by using a Mb-NAGase activity as a biomarker. Interestingly, a highly negative correlation between the lHGU and the specific Mb-NAGase activity was found. In fact, the environment was able to induce highly branched mycelia only under those culture conditions compatible with specific Mb-NAGase values equal to or higher than 190 U g dry.wt -1. These results could also indicate that the fungus adjusts its morphology in response not only to the surrounding substrate concentration (Lübbehüsen et al. 2004; Ziv et al. 2008), but also to the environmental culture condition as a whole.
In connection to the involving of wall lytic enzymes in hyphal morphology, a decrease of the lHGU is reported in some chitin synthase mutants as well. The lHGU for a ChsB/G (chsB disruption) Aspergillus oryzae strain is 52% lower than that of the wild type (A1560). In addition, the hyphal diameter in that mutant is significantly higher than in the A1560 strain (Müller et al. 2002). A similar morphological response is caused by the repression of a chsB gene expression. Ichinomiya et al. (2002) constructed a chsB-conditional mutant in which chsB is placed under an inducible promoter, such as the alcohol dehydrogenase gene promoter of Aspergillus nidulans. Thus, under repressing conditions, the mutant produces highly branched hyphae. These results could be also compatible with an increase of the wall lytic potential.
Results previously reported (Pera et al. 1997) as well as the experimentation presented here constitute evidence to support the following simple quantitative approach to tailor a desired fungal microscopic growth. It basically consists of three major steps: 1) to select a relative marker of the wall lytic potential, 2) to conduct in vitro dose–response assays of potential modifiers of the selected enzyme marker, and 3) to design fermentation conditions using those effectors that are compatible with the desired microscopic morphology. This methodology was successfully applied in some biotechnological processes involving eukaryotic cells. One of them is the improvement of citric acid production using A. niger MYA 135. It has long been established that highly branched mycelium and bulbous cells are associated with good citric acid yields (Papagianni 2007). In this connection, the presence of CaCl2 not only increases a NAGase purified extract activity (Pera et al. 1997) but also the addition of 0.5 g l-1 of this salt to the fermentation medium induces a highly branched mycelium with abundant bulbous cells. In addition, under this culture condition the uptake of phosphate and sucrose as well as the production of citric acid (90 g l-1) are increased by 15, 35 and 50%, respectively (Pera and Callieri 1997). On the contrary, the presence of FeCl3 in a range of 0.5 - 10.0 mM impaired a NAGase purified extract activity (Pera et al. 1997). Thus, as it was mentioned before, the addition of 1 g l-1 FeCl3 to the BM encourages a scarcely branched mycelium and increases the production of both a mycelium-bound transesterification lipase activity (Colin et al. 2011) and an emulsifier compound (Colin et al. 2010a). Interestingly, in the same medium supplemented with 2% olive oil it was also observed that a specific extracellular hydrolytic lipase activity was increased by 6.6 fold after four days of incubation compared to the control (Colin et al. 2010b). Finally, another application is the enhancement of protoplast formation in Phaffia rhodozyma. This yeast displays an in situ β-D-glucosidase activity that is clearly increased by the presence of MnCl2. When P. rhodozyma grows in the presence of 4.0 mM MnCl2, the cells are bigger and rounder than those obtained in its absence, suggesting a weakening of the cell wall. Protoplasts are produced from these cells using KCl as an osmotic stabilizer (Pera et al. 1999). It might also be mentioned that P. rhodozyma feeding cells with weakened walls increases the efficiency of deposition of astaxanthin in the flesh of cultivated salmonids and crustaceans (Johnson 1989).
On the other hand, rheology-hyphal micromorphology relationships are particularly relevant in fermentation involving filamentous fungi. Bocking et al. (1999) reported that cultures of highly branched mutants are less viscous than those of the parental strains. They also found a linear relationship between the lHGU and the broth viscosity. In addition, Metz et al. (1981) in studies with Penicillium chrysogenum observed that the length of the hyphal elements decreased with increasing the power input per unit mass, as the increased agitation caused the hyphae to become shorter, thicker and highly branched. However, van Suijdan and Metz (1981) also found that the energy input required to reduce the hyphal length sufficiently to achieve a significant reduction in broth viscosity is enormous, and so broth viscosity reduction by this technique seems of little practical value. In this connection, the induction of a desired fungal microscopic pattern by permissible modification of environmental conditions could overcome that observation.
In summary, this work showed that both conidia adhesion capacity and hyphal morphology were among the governing factors affecting the final pellet diameter. It was also observed that once the pellet was formed the lHGU had an important influence on its final diameter. In addition, it was explored a new experimental procedure in order to quantitatively check the potential of some culture conditions to induce a determined hyphal morphology by using a Mb-NAGase activity as a biomarker. Besides, a practical and a quantitative method to check in few minutes the conidia adhesion capacity was also proposed. On the other hand, the information obtained was used to design culture conditions compatible with a desired form of fungal growth. Appropriate fungal morphologies are already successfully applied in some biotechnological processes.
Finally, if the results reported in the present article prove to be applicable to other fungal strains, manipulation of fungal morphology will be easier in industrial filamentous fungal fermentation.
This work was supported by grants PICT 2011–2158 (FONCyT), CIUNT 26/D409 (UNT) and PIP 297 (CONICET).
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