Professional Documents
Culture Documents
and Challenges
T.L. Chac on-Lee and G.E. Gonz alez-Mari no
Abstract: Microalgae have the potential to become a novel source of bioactive molecules, especially for those who
might wish to enhance the nutritional and functional quality of foods. Spirulina, one of the most popular microalgae, has
been described by the World Health Organization as one of the greatest superfoods on earth serving as an example of the
potential of microalgae. This review provides background on current and future uses of microalgae in the human diet,
lists the most common species of microalgae used to this end, and describes some production methods used in research
and industrial production and recovery. The review also discusses some of the difculties so far encountered such as low
productivities and recovery rates, as well as challenges in the production of compounds of interest. Many scientists and
engineers in research centers around the globe are currently dedicated to solve these problems as the various capabilities
of microalgae have caught the attention of the energy, environmental, and agricultural industries, we propose that the
food industry should as well evaluate the potential of microalgae as a novel source of health promoting compounds.
Introduction
Microalgae are microscopic photosynthetic organisms that are
found in both marine and freshwater environments. Their pho-
tosynthetic mechanism is similar to that of land-based plants.
They are generally more efcient in converting solar energy into
biomass, mainly because of their simple cellular structure and being
submerged in an aqueous environment with access to water, CO
2
,
and other nutrients. These organisms constitute a polyphyletic and
highly diverse group of prokaryotic and eukaryotic organisms. The
classication into divisions is based on various properties such as
pigmentation, chemical nature of photosynthetic storage prod-
uct, the organization of photosynthetic membranes, and other
morphological features. The most abundant microalgal classes
are Cyanophyceae (blue-green algae), Chlorophyceae (green al-
gae), Bacillariophyceae (including the diatoms), and Chryso-
phyceae (including golden algae) (Carlsson and others 2007).
Since the end of the Second World War (1945), many pri-
vate and public research groups have dedicated time and effort to
present microalgae to the public as a very important and plen-
tiful source of protein, based on its quality, and as one of the
best to be encountered. Since Tamiya and others (1963), who
under the sponsorship of the Carnegie Inst. reported that the mi-
croalgae Chlorella could be cultivated on a large scale, a great
deal of research has been reported regarding these tiny but very
special species. In the last 3 decades, there have been numerous
attempts by researchers and prot-seeking companies to commer-
MS 20100409 Submitted 4/14/2010, Accepted 7/3/2010. Authors are with the
Grupo de Procesos Agroindustriales at the Faculty of Engineering at the Univ. de
La Sabana, Campus Univ. Puente del Com un, Km 7 Autopista Norte de Bo-
got a, ChaCundinamarca, Colombia. Direct inquiries to author Gonz alez-Mari no
(E-mail: Gloria.gonzalez@unisabana.edu.co).
cialize production of microalgae and cyanobacteria. Some of these
companies have been in business for many years and are success-
fully producing biomass of these organisms and marketing it in
various forms (Gantar and Svir cev 2008). Despite this, microalgae
have not become the major source of food that was expected by
scientists when their nutritional properties were discovered.
It is important to agree upon common ground regarding what
we consider as food. According to author Hutton (2002) from the
Royal Society of Chemistry, Food is derived from plants, animals,
and microbes which are, in essence, highly organized chemical
systems. Many of the chemicals within food are essential for human
lifeothers just happen to be associated with the material we
actually want to eat. Some (avor and texture components and
color) actually persuade us to eat the food. We choose to eat
certain foods because of a combination of the chemicals they
contain that give it a pleasant taste and appearance and those that
we actually need in order to survive.
Humans are no strangers to the use of microalgae as a food
source, even if the commercial exploitation of this resource is only
a few decades old, since the early 1950s, when the focus was set
on a possible insufcient protein supply due to the rapid increase
of the world population (Spolaore and others 2006). Microalgae
appeared then as a good source of protein and has continued as
such, but with an increased interest due to the unique bioactive
ingredients recently found in these small microorganisms, which
gives them great potential as a food source and as a source of
functional molecules.
This review intends to give a critical point of view on the
technological possibilities of microalgae, an untapped resource
waiting to be exploited by professionals in the food science and
technology arena. The scope of the review goes beyond the highly
agreed-upon opinions about the use of species such as Chlorella,
Spirulina, Dunaliella, and others as a nutritional supplement and
c
2010 Institute of Food Technologists
Vol. 9, 2010
r
Comprehensive Reviews in Food Science and Food Safety 657
Microalgaepossibilities and challenges . . .
Table 1(Continued)
Topic of information Microalgae species Reference
Scenedesmus almeriensis S anchez and others 2008
Botryococcus braunii Mendes and others 2003
Arthrospira maxima
Various Burja and others 2001
Molina and others 2003
Pulz and Gross 2004
Singh and others 2005
Cardozo and others 2007
Plaza and others 2009
Inclusion of microalgae in foods or as food Spirulina platensis Morist and others 2001
Desmorieux and Hernandez 2004
Gouveia and others 2008a
Chlorella vulgaris Gouveia and others 2006, 2007a, 2008a
Andrade and others 2007
Schizochytriumsp. ANZFA 2002
Valencia and others 2007
Haematococcus pluvialis Gouveia and others 2006, 2008a
Isochrysis galbana Valenzuela-Espinoza and others 2002
Gouveia and others 2008b
Scenedesmus sp. Quevedo and others 2008
Anabaena Loreto and others 2003
Porphyridiumcruentum Guil-Guerrero and others 2004
Nannocloropsis spp.
Phaeodactylumtricornutum
Spirulina maxima Gouveia and others 2008a
Diacronema vlkianum
Various Liang and others 2004
Lee 1997
Table 2General composition (N% of dry matter) of different algae and comparison values with traditional sources of food.
Species Protein Carbohydrates Lipids
Spirulina platensis 63 (a) 15 (a) 11 (a)
61.32 to 64.43 (d) 15.09 to 15.81 (d) 7.09 to 8.03 (d)
Arthrospira maxima 60 to 71 (a) 13 to 16 (a) 6 to 7 (a)
Chlorella vulgaris 51 to 58 (a) 12 to 17 (a) 14 to 22 (a)
47.82 (d) 8.08 (d) 13.32 (d)
Chlorella pyreinodosa 57 (a) 26 (a) 2 (a)
Dunaliella salina 57 (a) 32 (a) 6 (a)
Porphyridiumcruentum 28 to 39 (a) 40 to 57 (a) 9 to 14 (a)
34.1 (c) 32.1 (c) 6.53 (c)
Scenedesmus obliquus 50 to 56 (a) 10 to 17 (a) 12 to 14 (a)
Aphanizomenon os-aquae 62 (a) 23 (a) 3 (a)
Chlamydomonas rheinhardtii 48 (a) 17 (a) 21 (a)
Anabaena cylindrica 43 to 56 (a) 25 to 30 (a) 4 to 7 (a)
Euglena gracilis 39 to 61 (a) 14 to 18 (a) 14 to 20 (a)
Spirogyra sp. 6 to 20 (a) 33 to 64 (a) 11 to 21 (a)
Synechococcus sp. 46 to 63 (a) 8 to 14 (a) 4 to 9 (a)
Nannocloropsis spp. 28.8 (b) 35.9 (b) 18.36 (b)
Haematococcus pluvialis 48 (e) 27 (e) 15 (e)
Isochrisis galbana 26.99 (d) 16.98 (d) 17.16 (d)
Conventional foods
Bakers yeast 39 (e) 38 (e) 1 (e)
Meat 43 (e) 1 (e) 34 (e)
Egg 47 (e) 4 (e) 41 (e)
Milk 26 (e) 38 (e) 28 (e)
Rice 8 (e) 77 (e) 2 (e)
Soya 37 (e) 30 (e) 20 (e)
Values expressed as percent dry matter.
(a) Becker 2007.
(b) Rebolloso-Fuentes and others 2001.
(c) Rebolloso-Fuentes and others 2000.
(d) Tokusoglu and
Unal 2003.
(e) Gouveia and others 2008a.
source of unlimited potent biologically active compounds, such
as carotenoids, phycobilins, fatty acids, polysaccharides, vitamins,
and sterols, which all deliver important benets to the human
consumer (Gouveia and others 2007a).
Micro- and macronutrients found in microalgae
Many analyses of gross chemical composition have been pub-
lished for different strains of microalgae under different growth
conditions (Tokusoglu and
Unal 2003; Becker 2004; Liang
and others 2004; Shimamatsu 2004; Spolaore and others 2006;
Rodriguez-Garcia and Guil-Guerrero 2008).
There are new evaluations of microalgal protein content, such
as the protein efciency ratio, the apparent biological value, and
the true digestibility value of protein content (Becker 2004). In
all of these tests, microalgae have compared favorably with the
reference and other food proteins in the amino acid content and
proportion and availability of amino acids in their protein prole
(Table 3).
658 Comprehensive Reviews in Food Science and Food Safety
r
Vol. 9, 2010
c
2010 Institute of Food Technologists
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2010 Institute of Food Technologists
Vol. 9, 2010
r
Comprehensive Reviews in Food Science and Food Safety 659
Microalgaepossibilities and challenges . . .
Microalgae are also a ne source of carbohydrates, found in
the form of starch, cellulose, sugars, and other polysaccharides.
The available carbohydrates have good overall digestibility and,
therefore, few limitations on their uses and applications.
The average lipid content in microalgae varies between 1% and
40% and, according to growing conditions, can be as high as 85%
of dry weight. Algal lipids are typically composed of glycerol, sug-
ars, or bases esteried to fatty acids, with carbon numbers in the
range of C
12
to C
22
. The most important lipids are the essen-
tial polyunsaturated fatty acids such as linoleic, eicosapentaenoic
(EPA), and docosahexaenoic (DHA). Probably the most valuable
compounds found in microalgae are the polyunsaturated fatty acids
because they are of great importance to human health (Table 4).
They are slightly higher in concentration than in sh oil, have less
chemical contamination than seafood lipids, and may have greater
purity after extraction (Pulz and Gross 2004). Oil from algae shows
additional benets as a long-chain PUFA supplier over sh oils,
including low taste intensity and off-odor problems (Valencia and
others 2007). Microalgae represent a valuable source of nearly all
important vitamins, which improve the nutritional value of algal
biomass.
Due to their phototrophic life, microalgae are often exposed to
high oxygen and free-radical stresses, which has resulted in the
evolution of numerous efcient protective systems against oxida-
tive and radical stressors. Among these protective systems is the
production of pigments, such as carotenes, chlorophylls, and phy-
cobiliproteins, all having high antioxidant and protective properties
(Pulz and Gross 2004).
Many toxicological trials are required for any new food item
before it can be declared safe for human consumption. Most of
these investigations are detailed toxicological tests to prove the
harmlessness of the product, like in the case of unconventional
protein sources, such as microalgae. By considering the available
information on possible toxic properties, or any other adverse
effects of the different algae tested so far, it can be stated that none
of them have shown negative effects. All tests, including human
studies, have failed to reveal any evidence that would restrict the
utilization of properly processed algal material (Becker 2007).
Commonly utilized microalgal species used for human
consumption
Microalgae such as Spirulina, Chlorella, Dunaliella, Haematococcus,
and Schizochytrium are classied as food sources falling into the
GRAS (Generally Regarded as Safe) category by the U.S. Food
and Drug Administration. Consequently, many high-value com-
pounds produced by microalgae can be administered as a powder
of dried or freeze-dried biomass with no extraction undertaken
(Walker and others 2005).
Among the most used microalgae are Chlorella and Spirulina,
in addition, Dunaliella, Haematococcus, Schizochytrium, Scenedesmus,
Aphanizomenon, Odontella, and Porphyridiumare gaining acceptance
in the food and health-food market. It might be useful to take a
brief look at what makes each of these microalgae special, both
from the consumer point of view, and from the point of view of
the food industry (Table 5), since their individual attributes will
allow for an adequate selection according to the need at hand.
Spirulina is one of the richest algal sources of -linolenic acid
(GLA). GLA is an essential polyunsaturated fatty acid and a po-
tent nutraceuticaI (Sajilata and others 2008). Various studies have
asserted its pharmaceutical value, especially in lowering the low-
density lipoprotein in hypercholesterolemic patients (Ishikawa and
others 1989) and alleviation of symptoms of premenstrual syn-
drome (Horrobin 1983) and atopic eczema (Biagi and others
1988). In vitro and in vivo studies have shown GLA to selectively
kill tumor cells without harming normal cells (Reddy and others
1998). GLA is also implicated in the amelioration of a number
of diseased states including schizophrenia, multiple sclerosis, der-
matitis, diabetes, and rheumatoid arthritis (Ziboh 1989; Sajilata
and others 2008).
Spirulina is an excellent source of phycobiliproteins. These com-
pounds are being studied due to their high free-radical scavenging
capacity, which could make them a potential antitumor and an-
ticancer drug (Hu 2004). Spirulina is a good source of vitamin
B1 (Desai and Sivakami 2004). Due to the easy bioavailability of
nutrients, including minerals, Spirulina may be a good choice for
women during pregnancy and lactation and is also benecial for
malnourished children. The World Health Organization (WHO)
has called Spirulina as one of the greatest superfoods on earth and
NASA considers it as an excellent compact food for space travel,
as a small amount can provide a wide range of nutrients (Khan and
others 2005). Spirulina has been incorporated in noodles, cook-
ies, nutritional bars, and other functional food products (Pulz and
Gross 2004). Spirulina also supports digestive functions and helps
to maintain bacteria in the gut.
Chlorella cells contain -1,3-glucan, an active immunostimula-
tor, which acts as a free-radical scavenger and as a reducer of blood
lipids (Becker 2004). A polysaccharide also found in Chlorella has
been linked to antitumor effects (Iwamoto 2004). Chlorella vulgaris
is also a rich source of proteins, 8 essential amino acids, vita-
mins (B-complex, ascorbic acid), minerals (potassium, sodium,
magnesium, iron, and calcium), -carotene, chlorophyll, CGF
(Chlorella growth factor), as well as other health-promoting sub-
stances (Rodriguez-Garcia and Guil-Guerrero 2008).
Dunaliella is known for its capacity to produce high concen-
trations of carotenes, especially -carotene. Among the other
carotenoids produced by Dunaliella are lutein, neoxanthin, zeaxan-
thin, violaxanthin, cryptoxanthin, and -carotene, which are gen-
erally marketed together as a carotenoid mix (Ben-Amotz 2004).
Haematococcus produces a carotenoid known as astaxanthin.
There is increasing evidence that astaxanthin surpasses -carotene,
zeaxanthin, canthaxanthin, vitamin C, and vitamin E regarding an-
tioxidant benets. Animal studies have shown that astaxanthin can
protect skin from UV radiation effects, protect against chemically
induced cancers, and enhance the immune system (Cysewski and
Lorenz 2004). It also has antiinammatory properties, which may
help alleviate arthritis, muscle pain, and carpal tunnel syndrome
(Walker and others 2005). Astaxanthin is a product of recent com-
mercialization and is sold under many different names, one of
which is BioAstin by Cyanotech Corp. (Kailua-Kona, Hawaii,
U.S.A.).
Porphyridium cruentum contains relatively rare polyunsaturated
fatty acids such as arachidonic acid and EPA, both important in
human nutrition (Arad and Richmond 2004).
Aphanizomen os-aquae is a cyanobacterium with a rather short
history of human consumption. Aphanizomen has many benecial
health effects such as antiinammatory, exhaustion relief, assisting
digestion, and general improvement of overall well being (Hu
2004).
Current Biomass Production Systems and Downstream
Processes
The chemical composition of microalgae is not an intrinsically
constant factor, it varies among strains and batch cultures, and
according to environmental parameters such as temperature, pH,
660 Comprehensive Reviews in Food Science and Food Safety
r
Vol. 9, 2010
c
2010 Institute of Food Technologists
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Vol. 9, 2010
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Vol. 9, 2010
r
Comprehensive Reviews in Food Science and Food Safety 663
Microalgaepossibilities and challenges . . .
mineral content of water, light exposure, and agitation, all of which
come down to the type of culturing method used, open or closed,
indoors or outdoors.
The factors to be considered in this selection include the biology
of the alga, the cost of land, labor, energy, water, and nutrients,
as well as climate (if the culture is outdoors) and the type of nal
product desired. These parameters can be controlled in such a way
that the metabolism of the microalgae will favor a high production
of the particular compound of commercial interest, such as fatty
acids or antioxidants among others (Sierra and others 2008).
An efcient algal separation process should be able to process
a large volume of broth, yield a product with a high dry weight
percentage, and require modest investment, low consumption of
energy, and low maintenance cost (Poelman and others 1997).
Currently, recovery of biomass operations from culture broth can
account up to 20% to 30% of the total cost of production of the
biomass (Molina and others 2003), thus there is need for future
research directed to diminish costs and increase efciencies in this
step of the production. Figure 2 compiles information regarding
commonly used production systems, with the parameters that af-
fect productivity of microalgae and the biomass recovery systems
currently in use.
Photobioreactor designs for biomass production
Most commercial systems used today are open-air systems. The
4 major types of open-air systems currently in use are shallow
big ponds, tanks, circular ponds, and raceway ponds. Open-pond
systems for microalgae are of easy construction and operation
(Borowitzka 1999), but have been inappropriate when high pro-
ductivity is desired. Before the 1990s, most systems for growing
microalgae were open pond and carrousel (circular) types, which
allowed cellular densities of up to 0.7 g cells per liter (Contreras-
Flores and others 2003). An open system usually was a closed-
circuit canal about 15 to 20 cm deep, with a paddle rotation
system able to move the culture medium all around the circuit.
It required a large area of land, but was economical to build and
operate (Borowitzka 1999). Unfortunately, productivity of these
systems seems to have reached its maximum, impairing somewhat
the further development of microalgae biotechnology.
Culturing microalgae in open ponds and raceways has been
well developed and is still in use, but only a few species can
be maintained in the traditional open systems, those that control
contamination by using highly alkaline or saline selective envi-
ronments (Molina and others 2001). An example of this kind of
system would be a Cyanotech Corp. (www.cyanotech.com) open-
pond operation for Spirulina and Haematococcus in Hawaii, and of
Earthrise Nutritionals (www.earthrise.com) for the production of
cyanobacteria for food in California (Spolaore and others 2006).
Open systems have other disadvantages, such as ease of contam-
ination, difculties with the recovery of biomass, and problems
with temperature control, which all must be taken into account
when selecting an outdoor system. These problems have led to the
Figure 2Commonly used production systems, parameters, and recovery operations for the production of microalgae.
664 Comprehensive Reviews in Food Science and Food Safety
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Vol. 9, 2010
c
2010 Institute of Food Technologists
Vol. 9, 2010
r
Comprehensive Reviews in Food Science and Food Safety 665
Microalgaepossibilities and challenges . . .
Table 6Processing parameters for the production of microalgae.
Processing parameters Microalgae used Reference
Culture medium Spirulina Soletto and others 2005
Oliveira and Vieira Costa 2006
Colla and others 2007
Chlorella vulgaris/emersonii Scragg and others 2002
Bertoldi and others 2006
Dunaliella salina/Bardawil G omez and others 2003
Zhu and Jiang 2008
Haematococcus pluvialis Kobayashi and others 1997
Brinda and others 2004
Isochrysis galbana Valenzuela-Espinoza and others 2002
Scenedesmus obliquus/almeriensis/sp. Becker 1984
Martnez and others 1999
Makulla 2000
Quevedo and others 2008
Porphyridiumcruentum F abregas and others 1998
Anabaena Loreto and others 2003
Various Piorreck and others 1984
Janssen and others 2000
Carbon dioxide consumption efciency Spirulina platensis Greque de Morais and Vieira Costa 2007
Soletto and others 2008
Chlorella vulgaris/sp./Buitenzorg Wijanarko and others 2004
Cheng and others 2006
Chiu and others 2008
Scenedesmus Greque de Morais and Vieira Costa 2007
General Camacho and others 1999
Kurano and Miyachi 2004
Biomass production Spirulina platensis Oliveira and Vieira Costa 2006
Oliveira and others 2009
Chlorella vulgaris/emersonii Scragg and others 2002
Haematococcus pluvialis Brinda and others 2004
Scenedesmus almeriensis/sp. S anchez and others 2008
Quevedo and others 2008
Isochrysis aff. Galbana Valenzuela-Espinoza and others 2002
Phaeodactylumtricornutum S anchez and others 2002
General Grobbelaar 2000
Molina and others 2003
Light source/supply/cycle/irradiance Spirulina platensis Wu and others 2005
Soletto and others 2008
Chlorella sorokiniana Ugwu and others 2007
Haematococcus pluvialis Garca-Malea and others 2006
Scenedesmus almeriensis S anchez and others 2008
Phaeodactylumtricornutum S anchez and others 2002
Chlamydomonas reinhardtii Janssen and others 2000
Dunaliella tertiolecta
Anabaena Loreto and others 2003
Cyanobacteria Jacob-Lopes and others 2009
Simmer and others 1994
General Pulz and others 1995
Molina and others 1999
Ogbonna and others 1999
Kommareddy and Anderson 2004
Grobbelaar 2009
Mass transfer General Thomas and Gibson 1990
Molina and others 1999
Dissolved oxygen Chlorella sorokiniana Ugwu and others 2007
Phaeodactylumtricornutum S anchez and others 2004
General Camacho and others 1999
Temperature Spirulina platensis Colla and others 2007
Chlorella sorokiniana Ugwu and others 2007
Scenedesmus almeriensis/obliquus Martnez and others 1999
S anchez and others 2008
General Hancke and others 2008
Biomass recovery and downstreamprocessing Spirulina platensis Morist and others 2001
Desmorieux and Hernandez 2004
Oliveira and others 2008
Chlorella vulgaris Hee-Mock and others 2001
Dunaliella salina Orset and others 1999
Ben-Amotz 2004
Zhu and Jiang 2008
General Bilanovic and Shelef 1988
Sukenik and others 1988
Chisti and Moo-Young 1991
Petrusevski and others 1995
Poelman and others 1997
Borowitzka 1999
Olaizola 2003
Molina and others 2003
Danquah and others 2009
Lee and others 2009
666 Comprehensive Reviews in Food Science and Food Safety
r
Vol. 9, 2010
c
2010 Institute of Food Technologists
Vol. 9, 2010
r
Comprehensive Reviews in Food Science and Food Safety 667
Microalgaepossibilities and challenges . . .
Figure 3Solar energy operated tubular photobioreactor.
to this observations was that, in the presence of daylight and/or
high growth rate phase (exponential phase), the microalgal cells
are actively photosynthesizing with a high metabolism rate and
unicellular mobility, and this retards their agglomeration rate and
therefore lowers their settling rate. On the other hand, microalgal
cells exposed to darkness and/or low growth rate phase (stationary
phase) do not photosynthesize, hence their metabolism rate is low
and this causes the cells to agglomerate and settle faster.
Flocculation is a method that has gained popularity for dewater-
ing microalgae biomass, but with limited applications in the food
industry because of the addition of substances to promote the
formation of aggregates or occules that are not allowed in food
processing, for example multivalent metal salts or cationic poly-
mers (Bilanovic and Shelef 1988). Bioocculation is an interesting
option, but one that has been considered to be unreliable (Bene-
mann and Oswald 1996). It is based on the possibility of inducing
the aggregation of cells by environmental stresses such as extreme
pH, nutrient depletion, or temperature changes. The difculty of
this method is achieving the desired aggregation of cells without
modifying the cell composition. In applications such as biodiesel
production from algal biomass, microbial occulation has rendered
very good results (Al-Shahwani and others 1986; No ue and others
1992; Hee-Mock and others 2001; Lee and others 2009). Finding
microbial occulants safe for human use would be of great interest
for the recovery of microalgal biomass.
Downstreamprocesses for biomass drying and preservation
Biomass drying can be achieved using sunlight shining onto heat
trays containing biomass and thus evaporate the residual water;
conventional ovens are used as well. But the most commonly used
methods are spray-drying and freeze-drying, the latter usually is
not economically feasible.
Desmorieux and Hernandez (2004) compiled information re-
garding traditional drying methods of spirulina at an industrial
level, according to their report paper, spray-drying is the com-
monly used method at the most important farms. Cyanotechs
patented Ocean Chill method is a process that combines the use
of spray-drying with air that has a very low concentration of oxy-
gen to protect sensitive nutrients from oxidation by this element.
Hot air is commonly used on semiindustrial farms and artisanal
production farms where the biomass paste is extruded into small
cylinders, placed on trays, and dried by convective hot air, or di-
rectly by sun exposure. Another method reported by Desmorieux
and Hernandez (2004) is that of adding freshly ltrated spirulina
to precooked and dried hot our, mixed, and dried until a low
moisture content is achieved.
Not much information can be found regarding the operational
parameters of these processes, since on a laboratory scale, freeze-
drying and oven-drying are commonly used as means of obtaining
dried weight measurements, and preserving the biomass for fur-
ther analysis, and these methodologies are not easily scalable or
economically feasible. Once the production of microalgae turns
to commercial and industrial scale, this information is not largely
published or is even protected by patents, some references can be
found in Table 4.
Oliveira and others (2008) characterize the thin-layer drying
of S. platensis utilizing experimental curves to determine the best
condition of drying. A statistical model was applied to analyze the
effects of independent variables (air temperature and solids) on the
response of solubility in acid medium. Desmorieux and Hernan-
dez (2004) reported problems encountered while drying spirulina
biomass using conventional drying methods, such as protein and
sugar losses occurring in a drying oven that varies according to
the temperature of the air, and they reported a higher loss of sugar
content (about 30%) compared to proteins (10% to 20%); at a tem-
perature of 60
C there was a higher loss of protein by convective
or infrared drying.
Desmorieux and Hernandez (2004) also reported that the best
method to recover proteins and total sugars was freeze-drying,
but Orset and others (1999) stated that freeze-drying of microal-
gae biomass is a time-consuming process that results in a highly
hygroscopic powder and is poorly applicable on a large scale.
Morist and others (2001) published a comprehensive research
report on the possibilities of spirulina biomass as an auto-
regenerative biological life support system for men in outerspace.
They designed a process for spirulina biomass recovery and fur-
ther treatment to be used as food in 2 forms, liquid and dry.
It includes washing, pasteurization, and spray-drying and they
presented discussions on biomass quality regarding potential mi-
crobial contamination and changes in composition during the
process.
Another of the great controversies surrounding the industrial
production of microalgae is the search for an adequate use for
the used-up spent culture medium that can no longer be reused
or concentrated. A proposal by us is that since these spent media
contain a high concentration of nutrients and exocellular products,
they could be used as biofertilizers, thus providing added value to
the process and by helping the overall production to be friendlier
to the environment. This alternative should be evaluated before
drawing any denite conclusion.
Future and Perspective of Microalgae Applications
in So-Called Health Foods
At the moment, even with all the studies referring to the possible
benets of incorporating microalgae in food, such as improving
cardiovascular systems (Khan and others 2005), their slimming
properties (Lyons and OBrien 2002), energizing properties (Desai
and Sivakami 2004), antioxidant capabilities (Lyons and OBrien
2002), and cholesterol and triglyceride lowering effects (Geppert
and others 2006), the most popular way to consume microalgae
is as a diet supplement in tablet, capsule, or powder form (Molina
and others 2003).
The incorporation of microalgal biomass into traditional prod-
ucts has been found inconvenient in some cases because of its
strong green color, shy taste, and odor, as well as its powdery
consistency. All these aspects constitute main areas in need of
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Microalgaepossibilities and challenges . . .
Figure 4Challenges for food scientists and engineers.
food scientists and engineers around the world, shouldering social
responsibility, and helping to achieve popularity and production of
microalgal-based foods in such a way that this nutritional product
may adequately reach people of lower incomes, especially preg-
nant women, babies, and young children in poverty-stricken areas
around the world.
Suggested approaches to use microalgae in healthy foods
The situation as described earlier shows a highly favorable
panorama for the development of foods with high nutritional con-
tents and functional properties. It is necessary to take into account
that to achieve this important goal, many technological challenges
must be surpassed rst, especially regarding new technologies in
food engineering. Figure 4 displays some of the challenges that
are yet to be surpassed regarding microalgae production and use
in foods.
A solution to the strong avor of microalgae might reside in
the production of exotic-avored snacks and foods, with microal-
gae incorporated, along with the traditional Asian and Indian
spices, which will give the Western consumer a chance to accept
these new tastes along with the new products, instead of forcing
a new taste, color, and odor into well loved, everyday foods. Or,
maybe, more technical solutions are needed, such as encapsulation
of biomass to provide masking and improved rheological proper-
ties, or identication and removal of odor-producing compounds,
allowing an increase of concentration of microalgae in foods. Ul-
timately, it is left in the hands of scientists and food engineers to
nd the best solution.
But beside the avor of microalgae and its impact on prod-
uct acceptability, there are still many other aspects that need to
be resolved from a food engineers point of view, but necessarily
with help from other related disciplines. These aspects regard the
stability of the functional compounds found in microalgae and
their bioavailability according to their structure and the food ma-
trix where they are included, as well as considerations concerning
preservation, packaging, and shelf life.
An additional challenge for the preservation processes of mi-
croalgae biomass is that of effectively entering nonthermic process-
ing technologies, which could greatly contribute to a reduction
in costs compared to processes like freeze-frying, while helping
to maintain intact all the properties of the protein and the func-
tional biomolecules of interest. Such technologies would involve
cryoconcentration, microwaves, and high pressures.
The industrial production of microalgal biomass also presents
itself with the technical challenges to obtain higher yields, lower
energy consumption rates, higher biomass recoveries, and lower
production costs in closed photobioreactors. These challenges are
not new, and many investigators have been, and are, currently at
work to improve microalgal photobioreactor performances and
biomass recovery systems. It is of great importance to also con-
duct studies regarding used-up culture media. Water conservation
programs and agricultural programs might nd interest, if the used
culture media can be utilized for irrigation of traditional crops,
especially if there are compounds present that might be bene-
cial for the preservation of the land or the growth and quality of
crops.
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