African Journal of Biotechnology
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African Journal of Biotechnology Vol. 2 (12), pp.620-630, December 2003 ISSN 1684-5315 © 2003 Academic Journals Review Utilization of fungi for biotreatment of raw wastewaters COULIBALY
Lacina1*, GOURENE Germain1, AGATHOS N Spiros2 1Laboratoire
d’Environnement et de Biologie Aquatique (LEBA), UFR-Sciences
et Gestion de l’Environnement,
Université d’Abobo-Adjamé, 02 BP 801 Abidjan 02, Côte d’Ivoire 2Unit
of Bioengineering, Catholic University of Louvain, Place
Croix du Sud 2 Bte 19, 1348 Louvain-la-Neuve, Belgium Corresponding
author. E-mail: lacina91@hotmail.com.
Phone: 00 (225) 07 49 71 53. Accepted 8 December 2003
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Fungal
biomasses are capable of treating metal-contaminated effluents with
efficiencies several orders of magnitude superior to activated carbon
(F-400) or the industrial resin Dowex-50. Additionally, fungal biomasses
are susceptible to engineering improvements and regeneration of their
capabilities. With regard to organic pollutants, excessive nutrients and
dyes, fungi can remove them from wastewaters, leading to a decrease in
their toxicities. However, the detoxification rates seem to be dependent
on media and culture conditions. The postreatement by anaerobic
bioprocesses of effluents that have been pretreated with fungi can lead to
higher biogas than the original effluents. In addition to the degradation
of organic pollutants, fungi produce added-value products such as enzymes
(LiP, MnP, Lacc, amylase, etc.) and single-cell protein (SCP). Most
research on fungal capacities to purify polluted effluents has been
performed on a laboratory scale, hence there is a need to extend such
research to pilot scale and to apply it to industrial processes. Key words: Wastewaters, effluents, fungi, biodegradation, biosorption, decolourisation, value-added treatment.
Abbreviations;
SCP: single-cell protein, LiP: lignin peroxidase, MnP: manganese
peroxidase, MIP: manganese independent peroxidase, Lacc: laccase, COD:
chemical oxygen demand, HTL: heat treatment liquor, BOD: biochemical
oxygen demand, OMW: olive mill wastewaters, WWTP: wastewater treatment
plant.
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Fungi
are recognized for their superior aptitudes to produce a large
variety of extracellular proteins, organic acids and other
metabolites, and for their capacities to adapt to severe
environmental constraints (Lilly and Barnett, 1951; Cochrane, 1958).
For example, Aspergillus
niger is the prototypical fungus for the production of citric
acid (Clark, 1962; Lal, 1980; Grewal and Kalra, 1995), homologous
proteins (esp. enzymes) and heterologous proteins (Archer et al.,
1994; Prasertsan et al., 1997; Radzio and Kuck, 1997; Wongwicharn et
al., 1999;
Xu et
al., 2000).
Moreover,Phanerochaete chrysosporium is the model of
white-rot fungi for the production of peroxidases (Bumpus et al.,
1985; Rodriguez et al., 1999). Beyond the production of such
relevant metabolites, fungi have been attracting a growing interest
for the biotreatment (removal or destruction) of wastewater
ingredients such as metals, inorganic nutrients and organic
compounds (Akthar and Mohan, 1986; Field et al., 1993; Feijoo and
Lema, 1995; Palma et al., 1999; Coulibaly, 2002). The focus of this review therefore concerns the use of fungi to remove or degrade various wastewater constituents. Some instances of synthetic wastewaters are reported, but only the contributions of fungal biomass in the biological treatment of raw wastewater are discussed in some length. |
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Domestic
sewage |
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Domestic sewage contains carbon and nutrient sources that can be removed by fungal biomass. In an early investigation, Thanh and Simard (1973) demonstrated the capacities of seventeen fungal biomasses to remove phosphates (84.1%), ammonia (73.3%), total nitrogen (68.1%) and chemical oxygen demand (COD) (39.3%). They obtained fungal growth on this effluent with an accumulation of biomass (451.2 mg l-1) that contained protein (47% g g-1). There was variability in fungal capacities as to the removal of pollutants (see Table 1). In fact, Trichothecium roseum was the best in phosphate removal (97.5%), whilst Epicoccum nigrum, Geotrichum candidum and Trichoderma sp. were the best in the removal of ammonia (84%), total nitrogen (86.8%) and COD (72.3%), respectively. Concerning cell-protein production, Paecilomyces carneus had the highest ratio of protein to biomass (92.5%). However, this fungus did not grow very well on domestic sewage. In our laboratory, domestic wastewater pretreatment by a strain of A. niger has been investigated under transient conditions. This fungal biomass removed about 72% of COD and 65% of protein (Coulibaly, 2002). Despite the differences between the bioprocess investigated in these two studies, COD and protein removal rates are in the same order. The overall feasibility of domestic wastewater treatment under sewer-simulating conditions has been explored recently both experimentally and by simulation (Coulibaly, 2002; Coulibaly et al., 2002; Coulibaly and Agathos, 2003). The heat treatment liquor (HTL) of an activated sludge was decolourised by Coriolus hirsutus (Fujita et al., 2000). This fungal strain exhibited a strong ability to decolourise HTL (70%) with an accumulation of manganese independent peroxidase (MIP) and manganese peroxidase (MnP). Optimising the culture medium by adding nitrogen and carbon sources and improving the biomass quality resulted in increased colour removal capacity by C. hirsutus (Kumar et al., 1998; Miyata et al., 2000; Fujita et al., 2000). Although fungal applications have shown good capacities on sewage treatment, they are still underutilised in practice. This could be explained, in part, by a widespread a priori assumption that fungal strains do not perform as well as bacteria.
Table 1. Examples of fungi used to treat domestic sewage, starch processing and metal bearing effluents. Optimal culture condition and the effect of fungal pretreatment are reported.
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Agroindustrial
effluents
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Industries
of olive oil, tapioca starch, distillery (molasses), cotton bleaching,
pulp and paper processing produce several billion litres of coloured,
often toxic and harmful wastewaters over the world annually. Those
effluents have strong concentrations of COD (10-200 g l-1),
phenol and its derivatives (0.5-8 g l-1) and often contain
proteins, cyanides, chlorinated lignin compounds and dyes (Borja et al.,
1992, 1997; Nieto et al., 1992; Bengtsson and Triet, 1994; Garcia et al.,
1997; Jimenez and Borja, 1997; Yesilada et al., 1998; Kahmark and Unwin,
1999). The large amount of lignin derivatives of these effluents is
responsible of
their dark-brown
colour (Calvo et
al., 1995). The phenolic compounds of such wastewaters exert some
bactericidal effects on wastewater treatment plant (WWTP) microorganisms (Borja
et al., 1996; Fang and Chan, 1997; Vassilev et al., 1997; Sayadi et al.,
2000). Fungal pretreatment (Table 2) of these effluents under aerobic
conditions makes it possible to obtain phenol reduction (51-100%), good
decolourisation (31-100%), biochemical oxygen demand (BOD) reduction up to
85.4%, and enzyme production (protease, Lacc (EC 1.10.3.2); LiP (EC
1.11.1.14), MnP (EC
1.11.1.13), amylase, etc.) (Vinciguerra et al., 1995; Yesilada et al.,
1995; Garcia et al., 1997, 2000; D’Annibale et al., 1998; Setti et al.,
1998; Gharsallah et al., 1999; Robles et al., 2000; Kissi et al., 2001). Amendment
of olive mill wastewater (OMW) composition (addition of co-substrate,
nutrients, salts) influences the removal of COD, phenols and colours (Yesilada
et al., 1998). In fact, Garcia et al. (2000) noted that G. candidum
removed COD but did not degrade phenols. However, by optimising OMW
composition (COD:N:S = 100:5:2) for G. candidum growth, Assas et
al. (2000) obtained a complete degradation of phenols and 70%
decolourisation. Miranda et al. (1996) maximized colour removal from
molasses wastewaters (up to 69%) with A. niger, after the amendment
of the culture medium with co-substrate and mineral nutrients (MgSO4,
KH2PO4 and NH4NO3). Some of
the consequences of OMW pretreatment by fungi are the 23- to 30-fold
higher increases in biogas production and the fertilizing effect on plants
(Trifolium repens) compared to non-pretreated effluent (Borja et
al., 1993, 1995 a,b,c; Jimenez and Borja, 1997; Vassilev et al., 1998).
Table 2. Examples of fungi used to treat distillery wastewaters. Optimal culture condition and the effect of fungal pretreatment are reported.
The
influence of co-substrate (see Table 3) upon paper and pulp industrial
wastewater treatment, detoxification and decolourisation rates has also
been observed with Ceriporiopsis subvermispora, P. chrysosporium,
Trametes versicolor, Rhizopus oryzae and Rhizomucor
pusillus (Manzanares et al., 1995; van Driessel and Christov, 2002;
Nagarathnamma and Bajpai, 1999; Nagarathnamma et al., 1999). The
mechanisms of decolourisation of agroindustrial effluents by fungi are
reported to include biosorption and/or biodegradation (Ohmomo,
1988; Sayadi and Ellouz, 1995; Soares and Duran, 1998; Christov et al., 1999; Nagarathnamma et al.,
1999). Some “mycoreactors” such as rotating biological contactor (MYCOR),
trickling filter reactor (MYCOPOR) and continuous column reactor have been
developed to decolourise pulp and paper wastewaters (Eaton et al., 1982;
Messner et al., 1990; Bajpai et al., 1993). These reactors were able to
run over several weeks by maintaining their colour removal rates.
Ligninolytic enzymes are also involved in the degradation of organic
compounds, including dyes (see below), within these effluents (Chivukula
et al., 1995).
The enzymatic oxidation mechanism of those pollutants has been well
discussed elsewhere and is not the aim of this contribution
(Young and
Yu, 1997;
Mester and
Tien, 2000). Beneficial effects of the fungal pretreatment of pulp
mill effluent upon its subsequent anaerobic digestion have been reported (Feijoo
et al., 1995). Anaerobic digestion of Kraft pulp mill effluent pretreated
by P. chrysosporium gave increased degradation of high molecular
weight compounds (79%) according to these authors. Also, an important
decolourisation (79%) was also observed, that was correlated with MnP
accumulation.
Table 3. Examples of fungi used to treat wood processing wastewaters. Optimal culture condition and the effect of fungal pretreatment are reported.
With regard to other agroindustrial wastewaters that are relatively non toxic (e.g. dilute lignocellulosics, starch, rice and mussels processing, sauce production, etc.) (see Table 1), fungal growth on them has been reported to produce single-cell protein (SPC), enzymes, chitosan, amylolytic preparations and a good reduction of COD (up to 97.8%) (Morimura et al., 1992, 1994 a,b; Murado et al., 1993; Kida et al, 1995; Yang and Lin, 1998; Yokoi et al., 1998; Jin et al., 1998, 1999, 2001).
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Dyed
effluents
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The
effluents of pharmaceutical industries, dyeing, printing, photographs,
textile and cosmetics contain dyes (McMullan et al, 2001). For example,
over 7 X 107 tons dyes are produced annually worldwide, of
which about 10% are lost in industrial effluent (Vaidya and Datye, 1982).
Wastewaters from textile industries are a complex mixture of many
polluting substances such as organochlorine-based pesticides, heavy
metals, pigments and dyes. Their compositions have been discussed in
detail by O’Neill et al. (1999). The majority of these dyes are slowly
removed by the WWTP, because of their toxicities to indigenous
microorganisms. Dye removal from wastewaters by established WWTP processes
are expensive and need careful application (Vandevivere et al., 1998;
Robinson et al., 2001). Furthermore, following anaerobic digestion,
nitrogen-containing dyes are transformed into aromatic amines that are
more toxic and mutagenic than the parent molecules (Shaul et al., 1985;
Chung and Stevens, 1993; Ganesh et al., 1994). To overcome these
difficulties, fungi are being investigated for their potential to
decolourise effluents. Among them, the most widely studied are the
white-rot fungi P. chrysosporium (a model, primarily laboratory
organism) and T. versicolor (a promising organism for industrial
applications). Nowadays other fungi have also shown some capacities to remove dyes from industrial effluents. Dyes are removed by fungi by biosorption (Contato and Corso, 1996; Tatarko and Bumpus, 1998; Payman et al., 1998; Zheng et al., 1999; Fu and Viraraghavan, 2000), biodegradation (Nigam et al., 1995; Conneely et al., 1999) and enzymatic mineralisation (LiP, MnP, manganese independent peroxidase (MIP), Lacc) (Young and Yu, 1997; Ferreira et al., 2000; Ollikka et al., 1998; Podgornik et al., 1999; Wong and Yu, 1999; Zheng et al., 1999; Pointing and Vrijmoed, 2000; Wesenberg et al., 2003). However, one or more of these mechanisms could be involved in colour removal, depending on the fungus used. Other fungal biomasses applied to the decolourisation of raw textile effluents include Botrytis cinerea, Endothiella aggregata, Geotrichum fici, R. oryzae, Tremella fuciformis, Xeromyces bisporus, Hirschioporus larincinus, Inonotus hispidus, Phebia tremellosa and C. versicolor (Banat et al., 1996; Kirby, 2000; Polman and Breckenridge, 1996). It is reported that raw effluents can only partially be decolourised upon fungal treatment (maximum of 49-80% but often much less). For example, a complex mixture of real textile effluents containing many reactive dyes could be decolourised upon partial dilution by using the agaric white-rot fungus Clitocybula dusenii (Wesenberg et al., 2002). The weak decolourisation of these effluents by complete cultures could be explained by the influences of temperature, pH, salts, inhibitory molecules (sulphur compounds, surfactants, heavy metals, bleaching chemicals), carbon and nutrients within these solutions (Chao and Lee, 1994; Jacob et al., 1998; Swamy and Ramsay, 1999; Mester and Tien, 2000). Concerning enzymatic (Lacc, LiP, MnP) degradations, these reactions are quite complicated, involving numerous low molecular weight cofactors that serve as redox mediators (Reyes et al., 1999; Wesenberg et al., 2003). These cofactors, in addition to the enzymes themselves, influence fungal colour removal rates.
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Metal
containing effluents
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Metallurgical
industries, mining, surfaces cleaning, waste incinerators produce large
wastewater polluted by metals. Dissolved metals escaping into the
environment pose a serious health hazard. Because they accumulate in
living tissues throughout the food chain, which has human at its top.
There is a need to remove heavy metals before they enter the complex
ecosystem. Physicochemical treatments evolved in very diluted
water-containing metals (precipitation, electrochemical, flocculation,
coagulation, ion exchange) are expensive. Utilization of biomasses in
general (Volesky, 1994; Veglio and Beolchini, 1997; Kratochvil and Volesky,
1998; McKay et al., 1999; Gupta et al., 2000) and particularly that of
fungi are considered to be best alternatives for those waters purification
(Kapoor and Viraraghavan, 1995; Modak and Natarajan, 1995; Sag et al.,
1998; Volesky and Holan, 1995; Atkinson et al., 1998; Kratochvil and
Volesky, 1998; Mogollon et al., 1998; Savvaidis, 1998; Tobin and Roux,
1998). Indeed, the purification of the water-containing metals by fungal
biomass is cheaper and it presents the following advantages: (i)
production of residual small volume; (ii) possibility of valorisation of
fungal waste biomasses from industrial fermentations; (iii) fast removal
and (iv) easy installation of the process.
Fungal
biomasses walls are composed of macromolecules (chitin, chitosan, glucan,
lipid, phospholipides), which contain carboxyl groups (R-COOH), amino
groups (R2NH, R-NH2), phosphates, lipids, melanin,
sulphates (R-OSO3-) and hydroxides (OH-)
(Caesartonthat et al., 1995; Kapoor and Viraraghavan, 1998 a,b; Fogarty
and Tobin, 1996; Kapoor et al., 1999). Those functional groups are metals
sorption sites (Tsezos and Volesky, 1982; Mullen et al., 1992; Guibal et
al., 1995; Gardea Torresdey et al., 1996; Kapoor and Viraraghavan, 1997;
Matheickal and Yu, 1997; Zhang et al., 1998; Sarret et al., 1999; McHale
and McHale, 1994; Mashitah et al., 1999; Tereshina et al., 1999; Zhou,
1999). Fungi remove metals essentially by adsorption, chemisorptions (ion
exchange), complexation, coordination, chelation, physical adsorption and
microprecipitation (Guibal et al., 1995; Huang and Huang, 1996; Kapoor and
Viraraghavan, 1997; Sarret et al., 1998). There are also possible oxydo-reduction
taking place in the biosorbent. When metals are removed by ionic exchange,
they generally replace K+, Mg2+, Ca2+ and
H+ contained in biomasses (Akthar et al., 1995; Zhou, 1999;
Gomes et al., 1999; Mashitah et al., 1999). Table 1 gives a synthesis of
some works on metals removal from wastewaters by some fungi. Biomasses
used to remove metals from wastewaters are generally produced against few
residual biomasses from fermentation (Fourest et al., 1994; Meyer and
Wallis, 1997). Metals sequestrations by fungi are influenced by the
mineral and organic compositions content of the medium in which biomasses
are produced. Biomasses granulometries and physiological states (living or
dead), co-ions, metals concentrations and physical parameters
(temperature, pH, ionic force, presence of others metals) influence also
metals removal from polluted waters (Volesky, 1994; Akthar et al., 1995;
Gomes and Linardi, 1996; Modak et al., 1996; Gardea Torresdey et al.,
1997; Yu and Kaewsan, 1999; Zhou, 1999). Metals by fungi from various raw
effluents (gold
mining effluent, tanning effluent, swine water, polluted
lake waters)
are sometimes completely removed (see Table 1). However, these outputs
depend on the metal and fungus involved.
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Discussion
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Essential works on fungal utilization for raw wastewaters biopurification
have been laboratory tests. This situation can be explained by the fact
that fungal utilization in environmental biotechnology is still under
investigation to assess information’s on process implementation. To gain
confidence with the results, these investigations are performed on
synthetics wastewaters. The good results obtained in laboratory tests
depend on growth
medium optimisation (addition of co-substrate, nutrients, mediators
molecules, physical parameters optimisation) and a good handling of
biomasses. However, these works amongst other things prove some advantages
when a mycoreactor is introduced in effluents treatment lines. In fact,
there are some reductions of bactericidal effects and an increase in
biogas production. Consequently work on pilot and the development of
treatment plants are to be encouraged. The
degradation and the mineralisation of some recalcitrant dyes and
organochlorinated compounds are effective by certain white rot fungi.
However fungal aptitudes for raw wastewaters remain dependent on salts
concentration, culture conditions and especially on the amendment of
carbon and nutriment sources. Among
the co-susbstrates tested for effluent pretreatment by fungi, glucose and
sucrose were the best, when they were used at 5 to 10 g l-1. To
minimise the mycoreactor integration cost in the treatment line, the
co-substrate could be provided by feeding the reactors with amylaceous
effluents or others wastewaters rich in sucrose or glucose as these carbon
sources proved to be the best co-substrate. About the growth medium impact
on fungal capacities to decolourise HTL, one could use C. hirsutus
in post processing of an activated wastewater, because of its sensitivity
to organic nitrogen. The oxidoreductases activities could be more
significant, thanks to the use of substrate that could ensure the role of
mediators’ molecules and guarantee the generation of H2Ò2
in the reaction medium. Salts constraint could be overcome while
proceeding to the desalinisation of the effluents before their treatment
with fungi. |
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Conclusion
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This
review highlighted the capacities of certain fungi to pretreat raw
wastewaters. However, essential works on this subject are still
laboratories tests and they are of less industrial scale application. The
white rot fungi are suitable for the degradation of a large variety of
pollutants and to produce at the same time metabolites of great added
values (proteins, enzymes). However, an optimisation of the culture media
in carbon sources or nutrients and mediators molecules is very important
to obtain a good output of pollutants degradations. With
regard to other fungi, those also contribute to effluents purification
with proteins and enzymes productions (for example, A. awamory and A.
niger). Some residual biomasses from fungal fermentation, have been
used to remove metals and dyes from effluents. Ultimately, the fungal
biomasses present many assets for biopurification of wastewaters. Acknowledgements This research was supported by a fellowship of The Ministry of Higher Education, Scientific Research and Technological innovation of Côte d’Ivoire. We thank all of our colleagues from LEBA and Unit of Bioengineering for their useful discussions. |
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