Bioconversion of Gelatinised Sago Starch to Fermentable Sugar Using Recombinant Saccharomyces Cerevisiae
Bioconversion of sago starch to fermentable sugar was investigated using three genetically modified Saccharomyces cerevisiae strains, YKU107 (expressing α- amylase), YKU131 (expressing glucoamylase) and YKU 132 (expressing α-amylase and glucoamylase). Alpha-amylase (YKU107) and glucoamylase (YKU1...
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| Format: | Thesis |
| Language: | English English |
| Published: |
2004
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| Online Access: | http://psasir.upm.edu.my/id/eprint/24/ http://psasir.upm.edu.my/id/eprint/24/1/FSMB_2004_16.pdf |
| _version_ | 1848838674730450944 |
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| author | Mohamad Nazri, Azlian |
| author_facet | Mohamad Nazri, Azlian |
| author_sort | Mohamad Nazri, Azlian |
| building | UPM Institutional Repository |
| collection | Online Access |
| description | Bioconversion of sago starch to fermentable sugar was investigated using three
genetically modified Saccharomyces cerevisiae strains, YKU107 (expressing α-
amylase), YKU131 (expressing glucoamylase) and YKU 132 (expressing α-amylase
and glucoamylase). Alpha-amylase (YKU107) and glucoamylase (YKU131) was
partial purified using acetone and ammonium sulphate precipitation, respectively
before characterisation studies were carried out. The enzymes were purified by about
2.78 and 1.08 fold with recovery of 41.93% and 33.64%, respectively. Through
DEAE-cellulose column chromatography, only 26.31% α-amylase and 36.68%
glucoamylase were recovered with purification fold of 6.90 and 1.81. Futher
characterisation showed that both enzymes were stable at pH 5.5, temperature 30oC
and ionic strength of 0.05 M, evidenced with residual activity higher than 90%.
Optimum pH, temperature and initial starch concentration for glucose production
were determined as 5.5, 30oC and 20gL-1, respectively. From influence of various
starches studied, potato starch was hydrolysed efficiently, followed by corn, sago,
cassava and rice starch. However, the maximum yield of glucose based on utilised
starch followed the sequence: sago > corn > potato > cassava > rice starch. Batch
fermentation using 2 L fermenter showed that strains YKU107, YKU131 and
YKU132 were able to hydrolyse about 97.82%, 86.86% and 88.06%, respectively
during 60 hours cultivation with maximum glucose concentration of 9.32 gL-1, 3.63
gL-1 and 0.85 gL-1, respectively. Based on maximum glucose production, YKU107
was selected for futher studies. The influence of rpm examined by this strain
indicated that the glucose production consistently increased with rpm. Repeatedbatch
fermentation at maximum glucose concentration produced 6.91 gL-1 of
glucose and 12.35 gL-1 of biomass. The continuous culture was performed in order to
increase the glucose production. The maximum glucose concentration of 7.80 gL-1
was obtained at 0.075 h-1 dilution rate and suggested that the optimum operating
conditions for glucose production is just at the critical dilution rate. The plasmid was
categorised as stable even after 348 hours of continuous cultivation (43 residence
times). |
| first_indexed | 2025-11-15T06:59:19Z |
| format | Thesis |
| id | upm-24 |
| institution | Universiti Putra Malaysia |
| institution_category | Local University |
| language | English English |
| last_indexed | 2025-11-15T06:59:19Z |
| publishDate | 2004 |
| recordtype | eprints |
| repository_type | Digital Repository |
| spelling | upm-242013-05-27T06:45:05Z http://psasir.upm.edu.my/id/eprint/24/ Bioconversion of Gelatinised Sago Starch to Fermentable Sugar Using Recombinant Saccharomyces Cerevisiae Mohamad Nazri, Azlian Bioconversion of sago starch to fermentable sugar was investigated using three genetically modified Saccharomyces cerevisiae strains, YKU107 (expressing α- amylase), YKU131 (expressing glucoamylase) and YKU 132 (expressing α-amylase and glucoamylase). Alpha-amylase (YKU107) and glucoamylase (YKU131) was partial purified using acetone and ammonium sulphate precipitation, respectively before characterisation studies were carried out. The enzymes were purified by about 2.78 and 1.08 fold with recovery of 41.93% and 33.64%, respectively. Through DEAE-cellulose column chromatography, only 26.31% α-amylase and 36.68% glucoamylase were recovered with purification fold of 6.90 and 1.81. Futher characterisation showed that both enzymes were stable at pH 5.5, temperature 30oC and ionic strength of 0.05 M, evidenced with residual activity higher than 90%. Optimum pH, temperature and initial starch concentration for glucose production were determined as 5.5, 30oC and 20gL-1, respectively. From influence of various starches studied, potato starch was hydrolysed efficiently, followed by corn, sago, cassava and rice starch. However, the maximum yield of glucose based on utilised starch followed the sequence: sago > corn > potato > cassava > rice starch. Batch fermentation using 2 L fermenter showed that strains YKU107, YKU131 and YKU132 were able to hydrolyse about 97.82%, 86.86% and 88.06%, respectively during 60 hours cultivation with maximum glucose concentration of 9.32 gL-1, 3.63 gL-1 and 0.85 gL-1, respectively. Based on maximum glucose production, YKU107 was selected for futher studies. The influence of rpm examined by this strain indicated that the glucose production consistently increased with rpm. Repeatedbatch fermentation at maximum glucose concentration produced 6.91 gL-1 of glucose and 12.35 gL-1 of biomass. The continuous culture was performed in order to increase the glucose production. The maximum glucose concentration of 7.80 gL-1 was obtained at 0.075 h-1 dilution rate and suggested that the optimum operating conditions for glucose production is just at the critical dilution rate. The plasmid was categorised as stable even after 348 hours of continuous cultivation (43 residence times). 2004-03 Thesis NonPeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/24/1/FSMB_2004_16.pdf Mohamad Nazri, Azlian (2004) Bioconversion of Gelatinised Sago Starch to Fermentable Sugar Using Recombinant Saccharomyces Cerevisiae. Masters thesis, Universiti Putra Malaysia. Saccharomyces cerevisiae. Starch. Sago. English |
| spellingShingle | Saccharomyces cerevisiae. Starch. Sago. Mohamad Nazri, Azlian Bioconversion of Gelatinised Sago Starch to Fermentable Sugar Using Recombinant Saccharomyces Cerevisiae |
| title | Bioconversion of Gelatinised Sago Starch to Fermentable Sugar Using Recombinant Saccharomyces Cerevisiae |
| title_full | Bioconversion of Gelatinised Sago Starch to Fermentable Sugar Using Recombinant Saccharomyces Cerevisiae |
| title_fullStr | Bioconversion of Gelatinised Sago Starch to Fermentable Sugar Using Recombinant Saccharomyces Cerevisiae |
| title_full_unstemmed | Bioconversion of Gelatinised Sago Starch to Fermentable Sugar Using Recombinant Saccharomyces Cerevisiae |
| title_short | Bioconversion of Gelatinised Sago Starch to Fermentable Sugar Using Recombinant Saccharomyces Cerevisiae |
| title_sort | bioconversion of gelatinised sago starch to fermentable sugar using recombinant saccharomyces cerevisiae |
| topic | Saccharomyces cerevisiae. Starch. Sago. |
| url | http://psasir.upm.edu.my/id/eprint/24/ http://psasir.upm.edu.my/id/eprint/24/1/FSMB_2004_16.pdf |