Abstract:A novel method for simultaneous bioflocculation and pretreatment of algae is revealed. The method includes bioflocculation of precultured algae (Chroococcus sp.) using pellet forming filamentous fungus (Aspergillus lentulusFJ172995) resulting in nearly 100% harvesting within 6 h without addition of any nutrient and carbon source at the optimized fungal/algal (F/A) ratio of 1:3. The algal-fungal interactions require metabolically active fungus with opposite charge. The bioflocculation process is replicable at r… Show more
“…The present study can be closely related to the above-mentioned cases as it also reports extracellular secretions from A. fumigatus , mediating cell wall changes in the C. pyrenoidosa cells. These secretions might help A. fumigatus to provide signal to the C. pyrenoidosa cell and bring it into close vicinity for nutritional benefits or enzymatic degradation [32]. Similar phenomenon of microalgal–fungal attachment has been reported by our group with wide range of microalgal species encompassing green algae ( Chlorella sp.…”
Section: Discussionsupporting
confidence: 62%
“…Apart from biodiesel aspect, harvesting of microalgae using filamentous fungi also increases its biogas potential. Prajapati et al [32] reported enhanced bio-methane production from algal–fungal pellets due to the enzymatic degradation of microalgal cell wall by the fungi. All these studies show that harvesting algae with filamentous fungi is a favorable process for biofuel production.…”
Section: Discussionmentioning
confidence: 99%
“…However, the studies with co-cultivation of fungi and algae have reported the interaction time to be between 24 and 72 h [22, 25–31]. In a more straight-forward approach, it has been observed that the attachment of algal cells (green algae or cyanobacteria) to fungal pellets could take place within 4–6 h using pre-cultivated fungal biomass [12, 32]. Such interaction of algae and PFF [12] is intriguing as it does not follow the simple kinetics of bio-harvesting [13, 33, 34].…”
Section: Introductionmentioning
confidence: 99%
“…Relatively simple phytoplankton–parasitic fungal (Chytrids) interactions controlled by cell-to-cell contact also exist in nature, which are driven by chemotaxis [37]. In our recent studies, somewhat similar action of fungus was observed in algal–fungal pellets as fungus used algal cells as nutrient source by enzymatically degrading it [32]. However, what drives the interaction between C. pyrenoidosa and A. fumigatus at the molecular level is not clear.…”
Background
Algal harvesting is a major cost which increases biofuel production cost. Algal biofuels are widely studied as third-generation biofuel. However, they are yet not viable because of its high production cost which is majorly contributed by energy-intensive biomass harvesting techniques. Biological harvesting method like fungal-assisted harvesting of microalgae is highly efficient but poses a challenge due to its slow kinetics and poorly understood mechanism.
Results
In this study, we investigate
Aspergillus fumigatus
–
Chlorella pyrenoidosa
attachment resulting in a harvesting efficiency of 90% within 4 h. To pinpoint the role of extracellular metabolite, several experiments were performed by eliminating the
C. pyrenoidosa
or
A. fumigatus
spent medium from the
C. pyrenoidosa
–
A. fumigatus
mixture. In the absence of
A. fumigatus
spent medium, the harvesting efficiency dropped to 20% compared to > 90% in the control, which was regained after addition of
A. fumigatus
spent medium. Different treatments of
A. fumigatus
spent medium showed drop in harvesting efficiency after periodate treatment (≤ 20%) and methanol–chloroform extraction (≤ 20%), indicating the role of sugar-like moiety. HR-LC–MS (high-resolution liquid chromatography–mass spectrometry) results confirmed the presence of
N
-acetyl-
d
-glucosamine (GlcNAc) and glucose in the spent medium. When GlcNAc was used as a replacement of
A. fumigatus
spent medium for harvesting studies, the harvesting process was significantly faster (
p
< 0.05) till 4 h compared to that with glucose. Further experiments indicated that metabolically active
A. fumigatus
produced GlcNAc from glucose. Concanavalin A staining and FTIR (Fourier transform infrared spectroscopy) analysis of
A. fumigatus
spent medium- as well as GlcNAc-incubated
C. pyrenoidosa
cells suggested the presence of GlcNAc on its cell surface indicated by dark red dots and GlcNAc-specific peaks, while no such characteristic dots or peaks were observed in normal
C. pyrenoidosa
cells. HR-TEM (High-resolution Transmission electron microscopy) showed the formation of serrated edges on the
C. pyrenoidosa
cell surface after treatment with
A. fumigatus
spent medium or GlcNAc, while Atomic force microscopy (AFM) showed an increase in roughness of the
C. pyrenoidosa
cells surface upon incubation with
A. fumigatus
spent medium.
Conclusions
Results strongly suggest that GlcNAc prese...
“…The present study can be closely related to the above-mentioned cases as it also reports extracellular secretions from A. fumigatus , mediating cell wall changes in the C. pyrenoidosa cells. These secretions might help A. fumigatus to provide signal to the C. pyrenoidosa cell and bring it into close vicinity for nutritional benefits or enzymatic degradation [32]. Similar phenomenon of microalgal–fungal attachment has been reported by our group with wide range of microalgal species encompassing green algae ( Chlorella sp.…”
Section: Discussionsupporting
confidence: 62%
“…Apart from biodiesel aspect, harvesting of microalgae using filamentous fungi also increases its biogas potential. Prajapati et al [32] reported enhanced bio-methane production from algal–fungal pellets due to the enzymatic degradation of microalgal cell wall by the fungi. All these studies show that harvesting algae with filamentous fungi is a favorable process for biofuel production.…”
Section: Discussionmentioning
confidence: 99%
“…However, the studies with co-cultivation of fungi and algae have reported the interaction time to be between 24 and 72 h [22, 25–31]. In a more straight-forward approach, it has been observed that the attachment of algal cells (green algae or cyanobacteria) to fungal pellets could take place within 4–6 h using pre-cultivated fungal biomass [12, 32]. Such interaction of algae and PFF [12] is intriguing as it does not follow the simple kinetics of bio-harvesting [13, 33, 34].…”
Section: Introductionmentioning
confidence: 99%
“…Relatively simple phytoplankton–parasitic fungal (Chytrids) interactions controlled by cell-to-cell contact also exist in nature, which are driven by chemotaxis [37]. In our recent studies, somewhat similar action of fungus was observed in algal–fungal pellets as fungus used algal cells as nutrient source by enzymatically degrading it [32]. However, what drives the interaction between C. pyrenoidosa and A. fumigatus at the molecular level is not clear.…”
Background
Algal harvesting is a major cost which increases biofuel production cost. Algal biofuels are widely studied as third-generation biofuel. However, they are yet not viable because of its high production cost which is majorly contributed by energy-intensive biomass harvesting techniques. Biological harvesting method like fungal-assisted harvesting of microalgae is highly efficient but poses a challenge due to its slow kinetics and poorly understood mechanism.
Results
In this study, we investigate
Aspergillus fumigatus
–
Chlorella pyrenoidosa
attachment resulting in a harvesting efficiency of 90% within 4 h. To pinpoint the role of extracellular metabolite, several experiments were performed by eliminating the
C. pyrenoidosa
or
A. fumigatus
spent medium from the
C. pyrenoidosa
–
A. fumigatus
mixture. In the absence of
A. fumigatus
spent medium, the harvesting efficiency dropped to 20% compared to > 90% in the control, which was regained after addition of
A. fumigatus
spent medium. Different treatments of
A. fumigatus
spent medium showed drop in harvesting efficiency after periodate treatment (≤ 20%) and methanol–chloroform extraction (≤ 20%), indicating the role of sugar-like moiety. HR-LC–MS (high-resolution liquid chromatography–mass spectrometry) results confirmed the presence of
N
-acetyl-
d
-glucosamine (GlcNAc) and glucose in the spent medium. When GlcNAc was used as a replacement of
A. fumigatus
spent medium for harvesting studies, the harvesting process was significantly faster (
p
< 0.05) till 4 h compared to that with glucose. Further experiments indicated that metabolically active
A. fumigatus
produced GlcNAc from glucose. Concanavalin A staining and FTIR (Fourier transform infrared spectroscopy) analysis of
A. fumigatus
spent medium- as well as GlcNAc-incubated
C. pyrenoidosa
cells suggested the presence of GlcNAc on its cell surface indicated by dark red dots and GlcNAc-specific peaks, while no such characteristic dots or peaks were observed in normal
C. pyrenoidosa
cells. HR-TEM (High-resolution Transmission electron microscopy) showed the formation of serrated edges on the
C. pyrenoidosa
cell surface after treatment with
A. fumigatus
spent medium or GlcNAc, while Atomic force microscopy (AFM) showed an increase in roughness of the
C. pyrenoidosa
cells surface upon incubation with
A. fumigatus
spent medium.
Conclusions
Results strongly suggest that GlcNAc prese...
“…Furthermore, algal-fungal copelletization improved oil extraction efficiency because fungal secreted hydrolytic enzymes disrupted the thick cell walls of Tetraselmis suecica (Muradov et al, 2015). The same was seen between Aspergillus lentulus FJ172995 and Chroococcus sp., where algal and fungal cells formed a pellet, and nearly 100% of biomass settled down within 6 h at an optimized fungal/algal ratio of 1:3 (Prajapati et al, 2016).…”
Section: Downstream Processing Of Algal Biomass Using Symbiontsmentioning
SummaryMicrobes are ubiquitously distributed, and they are also present in algae production systems. The algal microbiome is a pivotal part of the alga holobiont and has a key role in modulating algal populations in nature. However, there is a lack of knowledge on the role of bacteria in artificial systems ranging from laboratory flasks to industrial ponds. Coexisting microorganisms, and predominantly bacteria, are often regarded as contaminants in algal research, but recent studies manifested that many algal symbionts not only promote algal growth but also offer advantages in downstream processing. Because of the high expectations for microalgae in a bio‐based economy, better understanding of benefits and risks of algal–microbial associations is important for the algae industry. Reducing production cost may be through applying specific bacteria to enhance algae growth at large scale as well as through preventing the growth of a broad spectrum of algal pathogens. In this review, we highlight the latest studies of algae–microbial interactions and their underlying mechanisms, discuss advantages of large‐scale algal–bacterial cocultivation and extend such knowledge to a broad range of biotechnological applications.
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