Optimization of ethanol, citric acid, and α-amylase production from date wastes by strains of Saccharomyces cerevisiae, Aspergillus niger, and Candida guilliermondii
Abstract:The present study deals with submerged ethanol, citric acid, and α-amylase fermentation by Saccharomyces cerevisiae SDB, Aspergillus niger ANSS-B5, and Candida guilliermondii CGL-A10, using date wastes as the basal fermentation medium. The physical and chemical parameters influencing the production of these metabolites were optimized. As for the ethanol production, the optimum yield obtained was 136.00 ± 0.66 g/l under optimum conditions of an incubation period of 72 h, inoculum content of 4% (w/v), sugars con… Show more
“…Monga et al (2011) have also reported the use of casein and peptone for the biosynthesis of amylase using various Aspergillus species. Acourene and Ammouche (2012) reported that urea was the most compatible elicitor for biosynthesis of amylase from A. niger which disagrees with the present findings.…”
Section: Discussioncontrasting
confidence: 99%
“…Aspergillus awamori nakazawa was also reported as an effective producer of glucoamylases and proteases in solid state fermentation with wheat bran as substrate (Negi and Banerjee, 2009). Acourene and Ammouche (2012) have produced α-amylase using three fungal strains, Saccharomyces cerevisiae, A. niger , and Candida guilliermondii from date wastes. Roses and Guerra (2009) have optimized production of amylase by A. niger using sugarcane bagasse as the substrate by solid-state fermentation.…”
Section: Discussionmentioning
confidence: 99%
“…and Rhizopus spp., probably due to their ubiquity and non-pretentious nutritional requirements. Substrates like vegetable waste, rice husk, banana peels (Khan and Yadav, 2011), wheat bran (Negi and Banerjee, 2010), date wastes (Acourene and Ammouche, 2012), sugarcane baggase (Roses and Guerra, 2009), wheat straw, rye straw, corncob leaf, oil cakes, and many others (Bhargav et al, 2008) have been utilized for the biosynthesis of amylases. Consequently, SSF process is of particular economic concern for such countries which have generation of huge plant biomass and agro-industrial wastes.…”
In this investigation, Aspergillus terreus NCFT4269.10 was employed in liquid static surface (LSSF) and solid state (SSF) fermentation to assess the optimal conditions for α-amylase biosynthesis. One-variable-at-a-time approach (quasi-optimum protocol) was primarily used to investigate the effect of each parameter on production of amylase. The maximum amylase production was achieved using pearl millet (PM) as substrate by SSF (19.19 ± 0.9 Ug−1) and also in presence of 1 mM magnesium sulfate, 0.025% (w/v) gibberellic acid, and 30 mg/100 ml (w/v) of vitamin E (~60-fold higher production of amylase) with the initial medium pH of 7.0 and incubation at 30 °C for 96 h. In addition, maltose, gelatin and isoleucine also influenced the α-amylase production. Amylase was purified to homogeneity with molecular mass around 15.3 kDa. The enzyme comprised of a typical secondary structure containing α-helix (12.2%), β-pleated sheet (23.6%), and β-turn (27.4%). Exploitation of PM for α-amylase production with better downstream makes it the unique enzyme for various biotechnological applications.
“…Monga et al (2011) have also reported the use of casein and peptone for the biosynthesis of amylase using various Aspergillus species. Acourene and Ammouche (2012) reported that urea was the most compatible elicitor for biosynthesis of amylase from A. niger which disagrees with the present findings.…”
Section: Discussioncontrasting
confidence: 99%
“…Aspergillus awamori nakazawa was also reported as an effective producer of glucoamylases and proteases in solid state fermentation with wheat bran as substrate (Negi and Banerjee, 2009). Acourene and Ammouche (2012) have produced α-amylase using three fungal strains, Saccharomyces cerevisiae, A. niger , and Candida guilliermondii from date wastes. Roses and Guerra (2009) have optimized production of amylase by A. niger using sugarcane bagasse as the substrate by solid-state fermentation.…”
Section: Discussionmentioning
confidence: 99%
“…and Rhizopus spp., probably due to their ubiquity and non-pretentious nutritional requirements. Substrates like vegetable waste, rice husk, banana peels (Khan and Yadav, 2011), wheat bran (Negi and Banerjee, 2010), date wastes (Acourene and Ammouche, 2012), sugarcane baggase (Roses and Guerra, 2009), wheat straw, rye straw, corncob leaf, oil cakes, and many others (Bhargav et al, 2008) have been utilized for the biosynthesis of amylases. Consequently, SSF process is of particular economic concern for such countries which have generation of huge plant biomass and agro-industrial wastes.…”
In this investigation, Aspergillus terreus NCFT4269.10 was employed in liquid static surface (LSSF) and solid state (SSF) fermentation to assess the optimal conditions for α-amylase biosynthesis. One-variable-at-a-time approach (quasi-optimum protocol) was primarily used to investigate the effect of each parameter on production of amylase. The maximum amylase production was achieved using pearl millet (PM) as substrate by SSF (19.19 ± 0.9 Ug−1) and also in presence of 1 mM magnesium sulfate, 0.025% (w/v) gibberellic acid, and 30 mg/100 ml (w/v) of vitamin E (~60-fold higher production of amylase) with the initial medium pH of 7.0 and incubation at 30 °C for 96 h. In addition, maltose, gelatin and isoleucine also influenced the α-amylase production. Amylase was purified to homogeneity with molecular mass around 15.3 kDa. The enzyme comprised of a typical secondary structure containing α-helix (12.2%), β-pleated sheet (23.6%), and β-turn (27.4%). Exploitation of PM for α-amylase production with better downstream makes it the unique enzyme for various biotechnological applications.
“…Using bioethanol instead of gasoline leads to the reduction of carbon emission by 80% and overall gasoline consumption by more than 30% (Elsanhoty et al, 2012). The production of bioethanol from lignocellulose raw materials requires generally the incorporation of an efficient pretreatment, followed by a scarification of the carbohydrates to obtain satisfactory effectiveness (Acourene and Ammouche, 2012). Compared to the use of gasoline, bioethanol helps to reduce CO 2 emission to about 80% (Li et al, 2008).…”
Date by-products constitute the principal food for the oasis populations in Middle East and North Africa. Dates contents consist of 70 to 80% of reducing sugars, and do not require an intensive energy and labour for thermophysical pre-treatment. They can serve as a good feedstock for bioethanol generation through fermentation and distillation. Algeria is among the top sixth producers of dates in the world with more than 250,000 tons/year; from these, more than 30% can be lost for different reasons and may be of low quality. In the laboratory, after an alcoholic fermentation of the substrate of the date varieties, Teggaza and Lebghel (T & L) using bakery yeast at 30°C for 72 h, the distilled and rectified date juice generated the highest ethanol ( 88° and 90°) with acceptable productions of 2.5 and 2.78 mL/kg/h, and assessed scale efficiencies of 23.57 and 26.2%. This is unlike the one (ethanol; 50%) directly generated by chemical reaction using the same quantity of sugar. The efficiencies that were obtained seem satisfactory and encourage the great scaling development of bioethanol generation using date waste biomass abundant in Algerian Sahara.
“…On the other hand, the high level of sugarcane bagasse production after the completion of Khuzestan province projects (three million tons per year) and the problems caused due to its storage require a comprehensive measurement in the direction of its optimized utilization and citric acid production (6)(7)(8)(9)(10)(11)(12)(13)(14)(15)(16).…”
Background: Citric acid is produced in insignificant quantities in Iran. Despite its great range of utilizations, and from another aspect, high level of production of sugarcane bagasse, the related problems arising from maintenance of this acid require thinking of a measure in the direction of its optimal usage and production. Objectives: The objective of the present study is to obtain effectual variables in producing citric acid from sugarcane bagasse through Solid State Fermentation (SSF) method using Aspergillus niger mold and to optimize its mass production by employing Taguchi method.
Materials and Methods:The effective parameters such as spore inoculation level, methanol percentage, solvent type, spore age, humidity percentage, initial pH of substrate, fermentation period and temperature, initial sugar percentage, autoclaving duration, nitrogen source and etc. were studied for producing citric acid from sugarcane bagasse with respect to Tagouchi method. Results: By considering the findings obtained from the tests, the highest production rate of citric acid g/kg out of untreated sugarcane bagasse is 75.45 based on the consumed sugar and a yield of 15.1 g/kg of sugarcane was achieved per day. Application of sodium hydroxide and acid pretreated sugarcane bagasse increased the production of citric acid in such a fashion that the production rates were 97.81 g/kg and 87.32 g/kg of sugarcane bagasse, respectively, compared to sodium hydroxide and acid untreated sugarcane bagasse.
Conclusions:The obtained findings in the present study indicated that sugarcane bagasse is an ideal substrate in producing citric acid and the aforementioned process could be considered as a beneficial and cost-effective method in citric acid production.
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