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Article

Enhancing Monascus Pellet Formation for Improved Secondary Metabolite Production

by
Xizi Zhang
,
Huiqian Liu
,
Mengyao Zhang
,
Wei Chen
* and
Chengtao Wang
*
Beijing Advanced Innovation Center for Food Nutrition and Human Health, Beijing Engineering and Technology Research Center of Food Additives, School of Food and Health, Beijing Technology and Business University, Beijing 100048, China
*
Authors to whom correspondence should be addressed.
J. Fungi 2023, 9(11), 1120; https://doi.org/10.3390/jof9111120
Submission received: 13 October 2023 / Revised: 12 November 2023 / Accepted: 16 November 2023 / Published: 19 November 2023
(This article belongs to the Section Fungal Cell Biology, Metabolism and Physiology)
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Abstract

:
Filamentous fungi are well-known for their ability to form mycelial pellets during submerged cultures, a characteristic that has been extensively studied and applied. However, Monascus, a filamentous saprophytic fungus with a rich history of medicinal and culinary applications, has not been widely documented for pellet formation. This study aimed to investigate the factors influencing pellet formation in Monascus and their impact on citrinin production, a key secondary metabolite. Through systematic exploration, we identified pH and inoculum size as critical factors governing pellet formation. Monascus exhibited optimal pellet growth within the acidic pH range from 5 to 6, resulting in smaller, more homogeneous pellets with lower citrinin content. Additionally, we found that inoculum size played a vital role, with lower spore concentrations favoring the formation of small, uniformly distributed pellets. The choice of carbon and nitrogen sources also influenced pellet stability, with glucose, peptone, and fishmeal supporting stable pellet formation. Notably, citrinin content was closely linked to pellet diameter, with larger pellets exhibiting higher citrinin levels. Our findings shed light on optimizing Monascus pellet formation for enhanced citrinin production and provide valuable insights into the cultivation of this fungus for various industrial applications. Further research is warranted to elucidate the molecular mechanisms underlying these observations.

1. Introduction

Filamentous fungi play a pivotal role in various industrial processes, contributing significantly to the production of enzymes, organic acids, antibiotics, and cholesterol-lowering agents through fermentation [1]. In submerged culture, these fungi exhibit two primary forms: mycelium aggregates forming pellets and uniformly dispersed suspended mycelium, fostering uniform growth [2]. The process of filamentous fungal pellet formation has been extensively studied, revealing two distinct typologies: coagulation and non-condensing, as illustrated in Figure 1. Coagulation-type pellets result from the coalescence of numerous spores during the pre-fermentation phase, followed by spore germination and subsequent mycelial tip growth. In contrast, non-condensing pellets undergo spore germination preceding pellet formation [3]. Fungi cultivated in pellet form offer several advantages, such as low fermentation broth viscosity, ease of biomass harvesting, and efficient oxygen diffusion [4].
The production of fungal products, whether target products or secondary metabolites, varies based on the morphological characteristics of the fungus [5]. Metabolites produced in pellet form typically exhibit higher yields, while fungi growing in suspended mycelia are more conducive to enzyme production [6]. However, the choice of form depends on the fungus species and external conditions. For example, Aspergillus terreus, characterized by small-diameter mycelial spheres, provides a favorable environment for lovastatin synthesis [7]. Conversely, Aspergillus nidulans, existing in a dispersed mycelial form, demonstrates enhanced penicillin production [8]. Research by Sai jin et al. indicates that small mycelial pellets formed by Aspergillus niger as dispersed mycelial fragments yield higher citric acid compared to undispersed pellets [9]. Various cultivation factors, including pH, inoculum, nutrients, and trace metals, also intricately affect mycelial morphology. For instance, certain Rhizobium species have a high probability of forming pellets at high inoculum spore concentrations (up to 3 × 109 spores/L) [10], Penicillium chrysogenum strains require high pH values for pellet formation [11], and carbon sources play a pivotal role in Aspergillus terreus pellet formation [12]. Consequently, the study of fungal pellets has been predominantly limited to individual fungal species.
While previously reported fungal species growing in granules include Penicillium [13], Aspergillus [14], and Rhizopus [15], with Aspergillus niger being predominant, there is a paucity of literature on Monascus growing in pellets. Monascus, a filamentous saprophytic fungus, is renowned for its historical applications in medicine and food [16]. Monascus is known for its significant polyketide secondary metabolites, including pigments, Monacolin K, and citrinin. Despite extensive research into gene manipulation to eliminate citrinin production due to its nephrotoxic nature [17], few studies have explored the relationship between citrinin production and mycelial morphology. Stirring rates, for example, significantly impact Monascus red-pigment production, with higher rates resulting in greater pigment yield and shorter mycelial branches [18]. Moreover, nonionic surfactants have demonstrated the capacity to modulate pigment production and mycelial morphology during Monascus fermentation [19].
The primary objective of this study is to investigate the external factors influencing Monascus pellet formation, with a focus on optimizing pellet fermentation conditions. Additionally, this study aims to elucidate the relationship between pellet morphology and the secondary metabolite citrinin. The findings of this investigation provide valuable insights into the interplay between Monascus pellet morphology and citrinin production, laying a robust foundation for future applications and advancements in this field.

2. Materials and Methods

2.1. Strains and Media

The wild strain M. purpureus RP2, maintained in the laboratory on potato dextrose agar medium at 30 °C, was selected as the experimental strain. For liquid fermentation, M. purpureus RP2 was initially cultivated on potato dextrose agar medium at 30 °C for 4 days. Subsequently, the mycelium was subjected to two rounds of washing with 5 mL of sterile water and then filtered through sterile gauze to obtain the spore suspension. Freshly prepared spore suspensions, each containing 107 spores/mL, were then inoculated into 30 mL of potato dextrose broth and adjusted to a pH of 5.5 in its natural state. The inoculated cultures were incubated at 28 °C for 5 days under vigorous shaking at 180 rpm. All fermentation experiments were conducted in 100 mL conical flasks, each containing 30 mL of sterile medium.

2.2. Shaker Pelletizing: Screening Factors

Following preliminary assessments, the influence of various factors on pellet formation by Monascus was systematically screened. These factors encompassed pH, carbon source, nitrogen source, and spore concentration. A pH of 5.5 (the standardized optimal value) was employed as the baseline for all screened factors unless otherwise specified. The parameters under investigation included media pH at five levels (pH 4.0, 6.0, 7.0, 8.0, and 10.0) and spore concentration at five levels (1.5 × 103, 1.5 × 104, 1.5 × 105, 1.5 × 106, and 1.5 × 107 spores /mL). Additionally, various carbon sources, such as glucose, sucrose, mannitol, soluble starch, xylose, and citric acid (each at 15 g/L), were examined. Similarly, diverse nitrogen sources, including NH4Cl, peptone, yeast leavening, soybean meal, fish powder, and C5H8NNaO4 (each at 10 g/L), were investigated to evaluate their impact on fungal pellet formation. The pH of the media was adjusted using either 2 M NaOH or 2 M HCl.

2.3. Analytical Methods

The initial spore concentration was determined using a hemocytometer counter and a light microscope (Olympus CX43, Tokyo, Japan). To measure spore concentration, the spore solution was diluted 1000-fold before quantification. Mycelial morphology in submerged cultures was assessed through visual observation over a 72 h period, enabling the differentiation between mycelium and pellets. Pellet biomass was quantified utilizing the dry weight method. Specifically, a defined volume of fermentation broth was filtered through pre-weighed filter paper, and the mycelium was rinsed thrice with ultrapure water. Subsequently, the filter paper was dried to a constant weight at 60 °C to ascertain mycelium biomass (dry weight). The diameter of pellets was measured using a vernier caliper with a resolution of 0.01 mm, with the average diameter calculated from measurements of ten pellets.

2.4. Morphological Observation of M. purpureus Pellet

The morphology of the pellets was observed under an optical microscope. For more detailed observations, the micro-morphology of the pellets was examined using a su8020 scanning electron microscope (SEM; Hitachi, Ltd., Tokyo, Japan). After 5 days of liquid fermentation, the pellets were fixed using a 2.5% glutaraldehyde solution, followed by a dehydration process involving sequential ethanol solutions of varying concentrations. This dehydration procedure, lasting 10 min for each concentration and repeated twice, was utilized. Subsequently, the morphology of the pellets, post-gold spraying, was examined under SEM [20]. The internal mycelial structure of the pellets was observed by employing the paraffin sectioning technique. This method encompassed the fixation, staining, decolorization, re-staining, drying, and sealing of sections, culminating in the observation of pellet tissue under a microscope.

2.5. Measurement of Monascus Citrinin Production

To assess the citrinin content, the fermentation broth of Monascus was subjected to a pre-treatment procedure. One milliliter of the fermentation broth was mixed with 2 mL of chromatographic-grade methanol and then subjected to ultrasonic extraction, away from light, for 30 min. Subsequently, the mixture was placed in a water bath at 60 °C for 1 h and then allowed to cool to room temperature. The supernatant was obtained by centrifugation for 15 min and subsequently filtered through a 0.22 μm filter. Citrinin content was determined via high-performance liquid chromatography-mass spectrometry (HPLC/MS) under specified conditions. The analysis was conducted on an Agilent 1200 series HPLC system (Agilent, Santa Clara, CA, USA) coupled with a triple quadrupole mass spectrometer (Agilent 6460 system). The analytical column employed was an Agilent eclipse plus C18 (2.1 mm × 50 mm × 3.5 μm). Conditions for the analysis encompassed a mobile phase consisting of a 70:30 (v/v) mixture of 0.1% formic acid and acetonitrile, a flow rate of 0.4 mL/min, a detection temperature of 40 °C, an injection volume of 1 μL, electrospray ionization source (ESI) in positive ion mode, a spraying voltage of 3000 V, auxiliary gas at 200 °C, sphingoid gas flow rate at 11 mL/min, and sphingoid gas temperature at 325 °C. The analysis was conducted in multiple reaction monitoring (MRM) mode, and the characteristic ion pair for citrinin was 233/251.2.

2.6. Statistical Analysis

All experiments were performed in triplicate, and numerical data are expressed as mean ± standard deviation. Statistical analysis was conducted using GraphPad Prism 9.0, employing analysis of variance (ANOVA). Statistically significant differences were identified with p-values < 0.05 and <0.01.

3. Results

3.1. Effect of Initial pH on Pellet Formation

Interestingly, our investigation revealed robust pellet growth across a pH range of from 4.0 to 8.0, with a noticeable absence of pellet growth at an alkaline pH of 10.0. This observation can be attributed to the inherent negative surface charge typically exhibited by fungal spores, discouraging spore aggregation [21].
Upon closer examination, a consistent pattern emerged between pellet diameter and biomass in response to pH variations. Both parameters exhibited a reverse correlation with pH levels, as both pellet diameter and biomass decreased with increasing pH. For instance, compared to the substantial 25.64 ± 0.27 mm pellet diameter observed at an initial pH of 4.0 (Figure 2a), the pellet diameter notably reduced by 38.61%, 49.10%, and 62.24% when adjusting the medium pH to 6.0, 7.0, and 8.0, respectively. This trend was mirrored in the biomass of the pellets, as depicted in Figure 2b, where decreases of 53.75%, 56.5%, and 87.62% were observed at pH values of 6.0, 7.0, and 8.0, respectively, compared to the biomass at pH 4.0.
Remarkably, acidic conditions were found to be particularly conducive to the formation of well-defined pellets. Specifically, at pH 6.0, uniformly sized and well-segregated pellets were generated, characterized by an average diameter falling within the range from 1.4 to 1.6 mm. Conversely, at pH 4.0, although pellet size was relatively large, the pellets were not uniformly distributed, with an average diameter of 2.58 ± 0.19 mm. In contrast, at pH 8.0, pellet size was markedly smaller, with an average diameter of 0.97 ± 0.05 mm.

3.2. Effect of Different Carbon and Nitrogen Sources on Pellet Formation

In our investigation of the impact of six diverse carbon sources on pellet formation under an initial medium pH of 5.5, we observed variations in pellet formation among these sources. Notably, sucrose, xylose, mannitol, and soluble starch led to reductions of 32.10%, 56.72%, 17.17%, and 4.49%, respectively, in biomass compared to the glucose group (Figure 3a). Conversely, citric acid as the sole carbon source resulted in a 58.51% increase in biomass relative to glucose.
The choice of carbon source also influenced pellet diameter, with sucrose, mannitol, soluble starch, and citric acid contributing to increases of 2.40%, 10.51%, 17.15%, and 50.52%, respectively, in pellet diameter (Figure 3b). Xylose, however, led to a 37.48% decrease in pellet diameter. Interestingly, under carbon sources of soluble starch and xylose, a mixture of free-suspending mycelium and mycelium-forming clumps was observed.
Although citric acid yielded higher pellet biomass and diameter compared to the glucose group, visual examination revealed excessively large pellets with signs of autolysis in the central region. Consequently, our findings suggest that glucose is the preferred carbon source for optimal pellet formation.
For the effect of nitrogen sources on pellets, our study explored the impact of NH4Cl, peptone, yeast extract powder, soybean meal powder, fish meal, and C5H8NNaO4 as the sole nitrogen sources. NH4Cl, yeast extract powder, soybean meal powder, and C5H8NNaO4 significantly increased pellet biomass, resulting in respective enhancements of 49.14%, 52.17%, 48.39%, and 54.18% relative to peptone as the nitrogen source (Figure 4a). In terms of pellet diameter, NH4Cl, soybean meal powder, and C5H8NNaO4 decreased pellet diameter by 33.40%, 24.65%, and 8.84%, respectively, compared to peptone (Figure 4b). Yeast extract powder, as the sole nitrogen source, resulted in mycelium with uneven density distribution.

3.3. Effect of Inoculum Volume on Pellet Formation

In our study, inoculum volumes were set at 1.5 × 103, 1.5 × 104, 1.5 × 105, 1.5 × 106, and 1.5 × 107 spores/mL. Minimal pellet formation was observed at the 1.5 × 103 and 1.5 × 104 spores/mL levels. However, increasing the inoculum size led to elevated Monascus biomass, while pellet diameter exhibited a negative correlation with inoculum size. Relative to the 1.5 × 105 spores/mL concentration, biomass increased by 1.72-fold and 2.39-fold at the 1.5 × 106 and 1.5 × 107 spores/mL levels (Figure 5a), respectively, while pellet diameter decreased by 18.6% and 41.06% under these respective conditions (Figure 5b). Pellets tended to form at inoculum levels below 108 spores/mL, with higher concentrations favoring dispersed mycelial growth [22].

3.4. Relationship between Pellet Size and Citrinin

During the fermentation process, the intricate relationship between the production of secondary metabolites and the morphology of filamentous fungi becomes evident [23]. Varied pellet diameters seem to exert distinct influences on citrinin synthesis, with larger pellet diameters (average diameter of 2.04 ± 0.008 mm) correlating with higher citrinin content, while smaller pellet diameters (average diameter of 1.4 ± 0.07 mm) are associated with lower citrinin levels in the fermentation. This correlation is visually represented in Figure 6b, showcasing the differences in citrinin content across various pellet diameters, ranging from a few hundred micrometers to one mm (Figure 6c–e).
The internal structure of fungal pellets is characterized by a dense kernel of tightly packed hyphae [24]. While the conventional method for pellet analysis involves microscopic examination [25], this approach has limitations, including sample squeezing that can impact biomass size and the loss of three-dimensional pellet information. To comprehensively understand pellet morphology, we employed scanning electron microscopy (SEM) for both overall and internal pellet visualization, supplemented by paraffin sections to observe the internal mycelial structure.
SEM images at 170× and 1000× magnifications (Figure 7a) unveiled the formation of pellets through the interweaving of mycelium, creating gaps between the mycelial elements. In comparison, control pellets with a mean diameter of 1.7 ± 0.08 mm exhibited a looser surface, while smaller-diameter pellets were tightly ensconced by mycelium. Notably, the mycelium structure within larger pellets appeared relatively less dense than their smaller counterparts, facilitating the expulsion of metabolites.
For a more detailed examination of the internal mycelial structure, paraffin sections were prepared for mycelial pellets cultured for 168 h (Figure 7b). Optical microscopy at 40× and 200× magnifications revealed robust overall growth and a uniform, dense distribution of mycelium within smaller pellets (average diameter of 1.4 ± 0.07 mm). In contrast, larger pellets (average diameter of 2.04 ± 0.008 mm) displayed sparse mycelium that appeared lighter in color following staining. This detailed analysis provides valuable insights into the complex interplay between pellet morphology and citrinin production.

4. Discussion

Industrial fermentation processes encounter challenges with filamentous fungi, and the adoption of a pelletized growth form may present solutions to some of these issues [26]. While prior studies have explored various filamentous fungal species like Rhizopus [10], Aspergillus [27], and Penicillium [13], all demonstrating pellet growth, it was surprising that, before this investigation, there were no reports of Monascus exhibiting pellet morphology. In our study, we successfully induced Monascus to adopt pellet form by intentionally manipulating four key factors: pH (ranging from 4.0 to 10.0), carbon source selection (including glucose, sucrose, mannitol, soluble starch, xylose, and citric acid), nitrogen source variation (NH4Cl, peptone, yeast leavening, soybean meal, fish powder, and C5H8NNaO4), and spore concentration (ranging from 1.5 × 103 to 1.5 × 107 spores/mL). The morphological transformations in the pellets were closely monitored over a 168 h fermentation period. Furthermore, our investigation explored the correlation between citrinin production and pellet characteristics, revealing a noteworthy observation: pellets with smaller diameters exhibited lower citrinin levels.
In our study, we systematically examined the impact of various factors on Monascus pellet formation, with a particular focus on pH and inoculum size. The role of pH in shaping pellet morphology is well-established, although its effects can vary among different fungal strains [11]. Our findings underscored the pivotal role of pH in Monascus pellet formation, with acidic conditions, specifically in the pH range of form 5 to 6, proving to be particularly conducive. Previous research on Cordyceps sinensis Cs-Hk1 and Rhizopus oryzae has reported similar observations, where lower pH levels (around 3.3 to 2.6) promoted the development of small, uniformly distributed pellets [15,28]. In our study, Monascus pellets formed under acidic conditions exhibited distinct characteristics, including small diameters, uniform and densely packed internal distributions, robust pellet integrity, and lower citrinin levels. This aligns with the general trend observed in fungal spores, which are negatively charged and exhibit variations in surface charges and isoelectric points [21]. The negative charge of fungal spores, expressed through electrophoretic mobility or zeta potential, increases with higher pH values, inhibiting spore aggregation [29,30]. This was substantiated by experimental demonstrations showing that increased pH hindered spore adherence to negatively charged surfaces [31]. Additionally, pH significantly influences the hydrophobicity of proteins, particularly those with hydrophobic characteristics that strongly impact adhesion [32].
Conversely, higher pH levels (7 to 8) in our study led to reduced biomass production and uneven pellet distribution. This observation in Monascus aligns with the notion that, in general, an increase in pH impedes spore aggregation due to the heightened negative charge on the conidial cell wall surface. The robust association we observed between initial pH levels and well-defined pellet formation in Monascus, particularly favoring acidic conditions, adds valuable insights to the understanding of fungal pelletization dynamics. Our investigation highlights the intricate relationship between initial pH conditions and Monascus pellet morphology, emphasizing the favorable conditions for pellet development under acidic pH values (5–6).
In shaping the morphology of filamentous fermentation, critical factors such as the quantity, type, and age of the inoculum play pivotal roles. Our study focused on elucidating the impact of spore concentration, revealing noteworthy insights into Monascus pellet formation. Lower spore concentrations, specifically at 1.5 × 107 spores/mL, were associated with the development of small, uniformly distributed pellets. These findings align with the observed inverse relationship between spore quantity and pellet size in various Aspergillus species [33]. Similar trends, indicating a decrease in spore inoculum leading to the formation of larger pellets, were documented in the study conducted by Posch and Herwig [34]. Notably, there exists a discrepancy in the literature regarding the preferred inoculum concentrations for optimal pellet formation [35].
To reconcile these disparities, our study integrated insights from the morphological development of Aspergillus niger with spore inoculum analyses [36]. The observed trends may be attributed to the interplay between NH4+ uptake, glucosamine concentration, and dissolved oxygen levels. Higher inoculum concentrations appear to enhance mycelial aggregation through an accelerated NH4+-uptake rate, subsequently leading to the faster conversion and release of glucosamine. This released glucosamine acts as a cohesive substance, promoting mycelial aggregation and pellet formation. As the inoculum concentration continued to increase, we observed a reduction in pellet diameter, accompanied by significant changes in roughness and densification. Assigning specific factors responsible for mycelial aggregation and disaggregation proves challenging, as discussed in the review by Braun et al. [37]. Our results underscore the significance of the inoculum amount in determining mycelial morphology by influencing the internal environment of the fermentation broth and the overall fermentation rate.
Monascus, like other filamentous fungi, relies on organic carbon and nitrogen sources to support its growth, providing essential energy for fungal development. Our investigation explored the impact of various carbon and nitrogen sources on pellet formation, revealing diverse effects on Monascus morphology. Organic compounds crucial for fungal growth, including sugars like D-glucose, D-fructose, and D-sucrose, are readily assimilated and utilized by Monascus. Additionally, Monascus exhibits the capacity to utilize a spectrum of other compounds, such as polysaccharides, organic acids, amino acids, alcohols, and hydrocarbons [38]. In our experiment, different carbon sources, excluding citric acid, did not significantly decrease pellet size but influenced both biomass and pellet dimensions. All studied carbon sources yielded pellet sizes ranging from 1 mm to 3 mm, showcasing well-developed mycelium on the pellet surface, and stable-sized pellets were consistently observed. Notably, the medium supplemented with glucose as the carbon source exhibited the highest biomass, consistent with findings from other studies highlighting glucose as a preferred carbon source for biomass production [39]. Mycelia, recognized as pivotal sites for growth and branching [40], play a crucial role in the expansion of pellets. While the exact mechanism behind the influence of glucose on pellet size and biomass remains unclear, it is evident that glucose contributes to increased pellet size by directly providing energy and carbon.
Changes in nitrogen sources led to variations in both biomass and pellet diameter. Pellet diameters for all nitrogen sources, except yeast extracts, fell within the 1 mm–3 mm range and exhibited robust development. However, NH4Cl and C5H8NNaO4 resulted in a significant decrease in pellet size, aligning with similar findings in the work of Jonsbu et al. [41]. These salts were observed to induce a growth lag, effectively controlling pellet growth. Earlier reports emphasizing the promotion of pellet formation by organic nitrogen sources due to their nutrient-rich composition supporting cell growth were corroborated in our study [42]. Our investigation highlighted the profound impact of carbon- and nitrogen-source selection on Monascus pellet formation. These findings underscore the pivotal role of nutrient sources in shaping fungal morphology. Glucose emerged as the preferred carbon source for optimal pellet formation, while peptone and fish meal demonstrated favorability as nitrogen sources for promoting pelleting.
While the optimal pellet morphology for maximizing secondary metabolite production in Monascus remains undetermined, studies have demonstrated a positive correlation between productivity and specific features, such as short, swollen branches [43]. Generally, a less dense internal structure within pellets is associated with higher productivity, a trend observed in the highly productive lactic acid formation from the pellet morphology of Rhizopus oryzae [44]. Despite this, smaller pellets are often considered more compact and stable. The overall connection between pellet size and productivity underscores the importance of oxygen and substrate availability, highlighting the need for pellets with open channels for optimal productivity. In summary, the relationship between pellet morphology and productivity in Monascus fermentation is intricate, with attention to features like short, swollen branches and internal structure density playing a key role in secondary metabolite production.

5. Conclusions

In conclusion, the production of vital secondary metabolites by Monascus, including pigments, γ-aminobutyric acid, Monacolin K, and citrinin, is significantly influenced by changes in mycelial morphology. Our findings established a correlation between citrinin content and pellet diameter, indicating that larger pellets tend to exhibit higher citrinin content. This correlation may be attributed to the autolysis tendency of large-diameter pellets, leading to the elimination of metabolites due to their sparse distribution within the pellet structure.
To explore the growth of Monascus pellets, our study emphasized the pivotal roles of pH and inoculum size in pellet formation, highlighting the pH range from 5 to 6 as optimal for fostering pellet growth. Additionally, we uncovered a relationship between pellet diameter and citrinin content, demonstrating that smaller pellets harbor lower citrinin levels. Nevertheless, further research is imperative to unravel the underlying molecular mechanisms and key molecules that drive pellet formation in filamentous fungi.

Author Contributions

X.Z.: Conceptualization, Methodology, Investigation, Formal analysis, Writing—Original Draft. H.L.: Methodology, Formal analysis. M.Z.: Formal analysis, W.C.: Conceptualization, Investigation, Supervision, Writing—Review and Editing. C.W.: Conceptualization, Methodology, Investigation, Project administration, Funding acquisition. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by National Natural Science Foundation of China [grant number 32372298]; Beijing Municipal Natural Science Foundation-Beijing Municipal Education Commission Science and Technology Plan Key Joint Project [grant number KZ202010011016]; Xinjiang ‘Two Zones’ Science and Technology Development Plan Project [grant number 2022LQ02003]; Construction of China Food Flavor and Nutrition Health Innovation Center [grant number 19008023032]; Beijing Engineering Technology Research Center Platform Construction Project [grant number 19008022080]; The Construction of High-Precision Disciplines in Beijing-Food Science and Engineering [grant number 19008021085].

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Data will be made available on request.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Wei, L.; Yan, L.; Frear, C.; Shulin, C. A new approach of pellet formation of a filamentous fungus—Rhizopus oryzae. Bioresour. Technol. 2007, 98, 3415–3423. [Google Scholar]
  2. Pirt, S.J. A theory of the mode of growth of fungi in the form of pellets in submerged culture. Proc. R. Soc. London Ser. B Biol. Sci. 1966, 166, 369–373. [Google Scholar]
  3. Veiter, L.; Rajamanickam, V.; Herwig, C. The filamentous fungal pellet-relationship between morphology and productivity. Appl. Microbiol. Biotechnol. 2018, 102, 2997–3006. [Google Scholar] [CrossRef] [PubMed]
  4. Hille, A.; Neu, T.R.; Hempel, D.C.; Horn, H. Effective diffusivities and mass fluxes in fungal biopellets. Biotechnol. Bioeng. 2009, 103, 1202–1213. [Google Scholar] [CrossRef] [PubMed]
  5. Iram, A.; Ozcan, A.; Yatmaz, E.; Turhan, I.; Demirci, A. Effect of Microparticles on Fungal Fermentation for Fermentation-Based Product Productions. Processes 2022, 10, 2681. [Google Scholar] [CrossRef]
  6. Karahalil, E.; Coban, H.B.; Turhan, I. A current approach to the control of filamentous fungal growth in media: Microparticle enhanced cultivation technique. Crit. Rev. Biotechnol. 2019, 39, 192–201. [Google Scholar] [CrossRef] [PubMed]
  7. Saberi, A.; Jalili, H.; Nikfarjam, A.; Koohsorkhi, J.; Jarmoshti, J.; Bizukojc, M. Monitoring of Aspergillus terreus morphology for the lovastatin production in submerge culture by impedimetry. Biochem. Eng. J. 2020, 159, 107615. [Google Scholar] [CrossRef]
  8. Moore, J.; Bushell, M.E. The effect of morphology and oxygen uptake on penicillin production by Aspergillus nidulans in submerged culture. Mycol. Res. 1997, 101, 1237–1241. [Google Scholar] [CrossRef]
  9. Jin, S.; Sun, F.; Hu, Z.; Liu, L.; Li, J.; Du, G.; Li, Y.; Shi, G.; Chen, J. Improving Aspergillus niger seed preparation and citric acid production by morphology controlling-based semicontinuous cultivation. Biochem. Eng. J. 2021, 174, 108102. [Google Scholar] [CrossRef]
  10. Liu, Y.; Liao, W.; Chen, S. Study of pellet formation of filamentous fungi Rhizopus oryzae using a multiple logistic regression model. Biotechnol. Bioeng. 2008, 99, 117–128. [Google Scholar] [CrossRef]
  11. Metz, B.; Kossen, N.W.F. The growth of molds in the form of pellets–a literature review. Biotechnol. Bioeng. 1977, 19, 781–799. [Google Scholar] [CrossRef]
  12. Jia, Z.; Zhang, X.; Cao, X. Effects of carbon sources on fungal morphology and lovastatin biosynthesis by submerged cultivation of Aspergillus terreus. Asia-Pac. J. Chem. Eng. 2009, 4, 672–677. [Google Scholar] [CrossRef]
  13. Saraswathy, A.; Hallberg, R. Mycelial pellet formation by Penicillium ochrochloron species due to exposure to pyrene. Microbiol. Res. 2005, 160, 375–383. [Google Scholar] [CrossRef]
  14. Zheng, X.M.; Cairns, T.C.; Ni, X.M.; Zhang, L.H.; Zhai, H.H.; Meyer, V.; Zheng, P.; Sun, J.B. Comprehensively dissecting the hub regulation of PkaC on high-productivity and pellet macromorphology in citric acid producing Aspergillus niger. Microb. Biotechnol. 2022, 15, 1867–1882. [Google Scholar] [CrossRef] [PubMed]
  15. Zhou, Y.; Du, J.X.; Tsao, G.T. Mycelial pellet formation by Rhizopus oryzae ATCC 20344. Appl. Biochem. Biotechnol. 2000, 84–86, 779–789. [Google Scholar] [CrossRef] [PubMed]
  16. Chen, W.; He, Y.; Zhou, Y.; Shao, Y.; Feng, Y.; Li, M.; Chen, F. Edible Filamentous Fungi from the Species Monascus: Early Traditional Fermentations, Modern Molecular Biology, and Future Genomics. Compr. Rev. Food Sci. F. 2015, 14, 555–567. [Google Scholar] [CrossRef]
  17. Liu, W.W.; An, C.Y.; Shu, X.; Meng, X.X.; Yao, Y.P.; Zhang, J.; Chen, F.S.; Xiang, H.; Yang, S.Y.; Gao, X.; et al. A Dual-Plasmid CRISPR/Cas System for Mycotoxin Elimination in Polykaryotic Industrial Fungi. ACS Synth. Biol. 2020, 9, 2087–2095. [Google Scholar] [CrossRef]
  18. Kim, H.J.; Kim, J.H.; Oh, H.J.; Shin, C.S. Morphology control of Monascus cells and scale-up of pigment fermentation. Process Biochem. 2002, 38, 649–655. [Google Scholar] [CrossRef]
  19. Yang, X.; Dong, Y.; Liu, G.; Zhang, C.; Cao, Y.; Wang, C. Effects of nonionic surfactants on pigment excretion and cell morphology in extractive fermentation of Monascus sp. NJ1. J. Sci. Food Agric. 2019, 99, 1233–1239. [Google Scholar] [CrossRef]
  20. Shi, R.; Gong, P.; Liu, Y.; Luo, Q.; Chen, W.; Wang, C. Linoleic acid functions as a quorum-sensing molecule in Monascus purpureus-Saccharomyces cerevisiae co-culture. Yeast 2023, 40, 42–52. [Google Scholar] [CrossRef]
  21. Douglas, H.W.; Collins, A.E.; Parkinson, D. Electric charge and other surface properties of some fungal spores. Biochim. Biophys. Acta 1959, 33, 535–538. [Google Scholar] [CrossRef] [PubMed]
  22. Papagianni, M.; Moo-Young, M. Protease secretion in glucoamylase producer Aspergillus niger cultures: Fungal morphology and inoculum effects. Process Biochem. 2002, 37, 1271–1278. [Google Scholar] [CrossRef]
  23. Chen, G.; Wang, M.; Tian, X.; Wu, Z. Analyses of Monascus pigment secretion and cellular morphology in non-ionic surfactant micelle aqueous solution. Microb. Biotechnol. 2018, 11, 409–419. [Google Scholar] [CrossRef] [PubMed]
  24. Cox, P.W.; Paul, G.C.; Thomas, C.R. Image analysis of the morphology of filamentous micro-organisms. Microbiol. (Read. Engl.) 1998, 144, 817–827. [Google Scholar] [CrossRef] [PubMed]
  25. Posch, A.E.; Spadiut, O.; Herwig, C. A novel method for fast and statistically verified morphological characterization of filamentous fungi. Fungal Genet. Biol. 2012, 49, 499–510. [Google Scholar] [CrossRef]
  26. Nair, R.B.; Lennartsson, P.R.; Taherzadeh, M.J. Mycelial pellet formation by edible ascomycete filamentous fungi, Neurospora intermedia. AMB Express 2016, 6, 31. [Google Scholar] [CrossRef]
  27. Fujita, M.; Iwahori, K.; Tatsuta, S.; Yamakawa, K. Analysis of pellet formation of Aspergillus niger based on shear stress. J. Ferment. Bioeng. 1994, 78, 368–373. [Google Scholar] [CrossRef]
  28. Liu, Y.S.; Wu, J.Y. Effects of Tween 80 and pH on mycelial pellets and exopolysaccharide production in liquid culture of a medicinal fungus. J. Ind. Microbiol. Biotechnol. 2012, 39, 623–628. [Google Scholar] [CrossRef]
  29. Zhang, J.; Zhang, J. The filamentous fungal pellet and forces driving its formation. Crit. Rev. Biotechnol. 2016, 36, 1066–1077. [Google Scholar] [CrossRef] [PubMed]
  30. Lytle, D.A.; Johnson, C.H.; Rice, E.W. A systematic comparison of the electrokinetic properties of environmentally important microorganisms in water. Colloids Surf. B. 2002, 24, 91–101. [Google Scholar] [CrossRef]
  31. Lee, I.; Chung, E.; Kweon, H.; Yiacoumi, S.; Tsouris, C. Scanning surface potential microscopy of spore adhesion on surfaces. Colloids Surf. B. 2012, 92, 271–276. [Google Scholar] [CrossRef] [PubMed]
  32. Pascual, S.; De Cal, A.; Magan, N.; Melgarejo, P. Surface hydrophobicity, viability and efficacy in biological control of Penicillium oxalicum spores produced in aerial and submerged culture. J. Appl. Microbiol. 2000, 89, 847–853. [Google Scholar] [CrossRef]
  33. Prosser, J.I.; Tough, A.J. Growth mechanisms and growth kinetics of filamentous microorganisms. Crit. Rev. Biotechnol. 1991, 10, 253–274. [Google Scholar] [CrossRef] [PubMed]
  34. Posch, A.E.; Herwig, C. Physiological description of multivariate interdependencies between process parameters, morphology and physiology during fed-batch penicillin production. Biotechnol. Prog. 2014, 30, 689–699. [Google Scholar] [CrossRef] [PubMed]
  35. Znidarsic, P.; Komel, R.; Pavko, A. Influence of some environmental factors on Rhizopus nigricans submerged growth in the form of pellets. World J. Microbiol. Biotechnol. 2000, 16, 589–593. [Google Scholar] [CrossRef]
  36. Papagianni, M.; Mattey, M. Morphological development of Aspergillus niger in submerged citric acid fermentation as a function of the spore inoculum level: Application of neural network and cluster analysis for characterization of mycelial morphology. Microb. Cell Fact. 2006, 5, 3. [Google Scholar] [CrossRef]
  37. Braun, S.; Vecht-Lifshitz, S.E. Mycelial morphology and metabolite production. Trends Biotechnol. 1991, 9, 63–68. [Google Scholar] [CrossRef]
  38. Papagianni, M. Fungal morphology and metabolite production in submerged mycelial processes. Biotechnol. Adv. 2004, 22, 189–259. [Google Scholar] [CrossRef]
  39. Kumar, P.; Dubey, K.K. Mycelium transformation of Streptomyces toxytricini into pellet: Role of culture conditions and kinetics. Bioresour. Technol. 2017, 228, 339–347. [Google Scholar] [CrossRef]
  40. Celler, K.; Picioreanu, C.; van Loosdrecht, M.C.M.; van Wezel, G.P. Structured morphological modeling as a framework for rational strain design of Streptomyces species. Anton. Leeuw. Int. J. G. 2012, 102, 409–423. [Google Scholar] [CrossRef]
  41. Jonsbu, E.; Ellingsen, T.E.; Nielsen, J. Effects of nitrogen sources on cell growth and production of nystatin by Streptomyces noursei. J. Antibiot. 2000, 53, 1354–1362. [Google Scholar] [CrossRef] [PubMed]
  42. Wen, T.-c.; Li, G.-r.; Kang, J.-c.; Kang, C.; Hyde, K.D. Optimization of Solid-state Fermentation for Fruiting Body Growth and Cordycepin Production by Cordyceps militaris. Chiang Mai J. Sci. 2014, 41, 858–872. [Google Scholar]
  43. Papagianni, M. Advances in citric acid fermentation by Aspergillus niger: Biochemical aspects, membrane transport and modeling. Biotechnol. Adv. 2007, 25, 244–263. [Google Scholar] [CrossRef] [PubMed]
  44. Liao, W.; Liu, Y.; Chen, S. Studying pellet formation of a filamentous fungus Rhizopus oryzae to enhance organic acid production. Appl. Biochem. Biotechnol. 2007, 137, 689–701. [Google Scholar] [PubMed]
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Figure 1. Description of the process of coagulative and non-coagulative types of pellets.
Figure 1. Description of the process of coagulative and non-coagulative types of pellets.
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Figure 2. Effect of M. purpureus fermentation broth pH on diameter and biomass of pellets. (a) Diameter, (b) dry weight. Data labeled with different lowercase letters indicate significant differences (p < 0.05).
Figure 2. Effect of M. purpureus fermentation broth pH on diameter and biomass of pellets. (a) Diameter, (b) dry weight. Data labeled with different lowercase letters indicate significant differences (p < 0.05).
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Figure 3. Effect of carbon source in M. purpureus fermentation broth on diameter and biomass of pellets. (a) Dry weight, (b) diameter. Data labeled with different lowercase letters indicate significant differences (p < 0.05).
Figure 3. Effect of carbon source in M. purpureus fermentation broth on diameter and biomass of pellets. (a) Dry weight, (b) diameter. Data labeled with different lowercase letters indicate significant differences (p < 0.05).
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Figure 4. Effect of nitrogen source in M. purpureus fermentation broth on diameter and biomass of pellets. (a) Dry weight, (b) diameter. Data labeled with different lowercase letters indicate significant differences (p < 0.05).
Figure 4. Effect of nitrogen source in M. purpureus fermentation broth on diameter and biomass of pellets. (a) Dry weight, (b) diameter. Data labeled with different lowercase letters indicate significant differences (p < 0.05).
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Figure 5. Effect of M. purpureus spore addition on diameter and biomass of pellets. (a) Dry weight, (b) diameter. Data labeled with different lowercase letters indicate significant differences (p < 0.05).
Figure 5. Effect of M. purpureus spore addition on diameter and biomass of pellets. (a) Dry weight, (b) diameter. Data labeled with different lowercase letters indicate significant differences (p < 0.05).
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Figure 6. Determination of citrinin in the fermentation broth of M. purpureus. (a) Total ion flow diagram in fermentation broths, (b) content of citrinin in different pellet diameters. (c–e) Pellets of different diameters, (c) the average diameter of 1.7 ± 0.08 mm. (d) The average diameter of 1.4 ± 0.07 mm. (e) The average diameter of 2.04 ± 0.008 mm.
Figure 6. Determination of citrinin in the fermentation broth of M. purpureus. (a) Total ion flow diagram in fermentation broths, (b) content of citrinin in different pellet diameters. (c–e) Pellets of different diameters, (c) the average diameter of 1.7 ± 0.08 mm. (d) The average diameter of 1.4 ± 0.07 mm. (e) The average diameter of 2.04 ± 0.008 mm.
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Figure 7. Comparison of the morphology of pellets of different diameter sizes. (a) Scanning electron microscope observation of the microstructure of pellets at ×170 (left) and ×1000 (right). (b) Paraffin sections were observed under a light microscope at×40 (left) and ×200 (right).
Figure 7. Comparison of the morphology of pellets of different diameter sizes. (a) Scanning electron microscope observation of the microstructure of pellets at ×170 (left) and ×1000 (right). (b) Paraffin sections were observed under a light microscope at×40 (left) and ×200 (right).
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Zhang, X.; Liu, H.; Zhang, M.; Chen, W.; Wang, C. Enhancing Monascus Pellet Formation for Improved Secondary Metabolite Production. J. Fungi 2023, 9, 1120. https://doi.org/10.3390/jof9111120

AMA Style

Zhang X, Liu H, Zhang M, Chen W, Wang C. Enhancing Monascus Pellet Formation for Improved Secondary Metabolite Production. Journal of Fungi. 2023; 9(11):1120. https://doi.org/10.3390/jof9111120

Chicago/Turabian Style

Zhang, Xizi, Huiqian Liu, Mengyao Zhang, Wei Chen, and Chengtao Wang. 2023. "Enhancing Monascus Pellet Formation for Improved Secondary Metabolite Production" Journal of Fungi 9, no. 11: 1120. https://doi.org/10.3390/jof9111120

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