Enhanced Production of Bioactive Compounds from Shrimp-shell Waste in a Fed-batch Biodegradation
- Alternative Title
- 유가식 생물학척 분해에서 새우 컵질 폐기물로부터 생리활성 물질의 향상된 생산
- Abstract
- Biodegradation of shrimp shell powder using Bacillus cereus EW5 strain was conducted for 96 h in a bioreactor by batch, and fed-batch strategies and the production of bioactive compounds were assayed and compared. In batch degradation, the bioreactor was filled with 1575 ml of productive medium containing 1% shrimp shell powder and 175 ml (10%, v/v) inoculum. In fed-batch strategy, culture broth was fed during 14, 42, and 70 h of degradation periods with pulse addition at a constant rate of 46.80 ml/h. The final working volume was 1.75 L for batch and 3.0 L for fed-batch operation. The cell dry weight, reducing sugar production, antioxidant activity, TLC analysis, and DNA damage inhibition activity was determined. The result of the fed-batch degradation was better compared to the batch system. The highest amount of reducing sugar (0.297±0.05 mg/ml), antioxidant activity (DPPH, 92.35%, ABTS, 98.16%), was achieved during 48 h of degradation in fed-batch mode. The highest reducing power (at A700nm = 1.55 per ml) was recorded during 96 h of degradation in fed-batch mode. Periodic addition of substrate in fed-batch system leads the higher biomass production (34.57 g/L) which was 61.77% higher than the batch (21.37 g/L) biodegradation, and consequently higher reducing sugar, and higher antioxidant activity.
- Author(s)
- Harun Ar RASHID
- Issued Date
- 2018
- Awarded Date
- 2018.2
- Type
- Dissertation
- Keyword
- Shrimp-shell waste Bacillus cereus EW5 Bioreactor Bioactive compounds Fed-batch biodegradation.
- Publisher
- 부경대학교
- URI
- https://repository.pknu.ac.kr:8443/handle/2021.oak/13900
http://pknu.dcollection.net/common/orgView/200000010520
- Affiliation
- 부경대학교 글로벌수산대학원
- Department
- 글로벌수산대학원 국제수산과학협동과정
- Advisor
- 김중균
- Table Of Contents
- Table of Contents····················································································i
List of Figures·······················································································iv
Abstract·······························································································v
Abbreviations······················································································vii
1. Introduction·······················································································1
2. Materials and Methods··········································································4
2.1. Strain culture medium·········································································4
2.2. Optimization of culture condition ···························································5
2.3. Batch and fed-batch biodegradation in bioreactor·········································6
2.3.1. Batch biodegradation ·······································································9
2.3.2. Fed-batch biodegradation ··································································9
2.4. Biomass concentration·······································································10
2.5. Measurement of reducing sugar ·········· ·················································11
2.6. Antioxidant activity of biodegraded SSW ················································13
2.6.1. DPPH radical scavenging assay ·························································13
2.6.2. ABTS radical cation decolorization assay··············································14
2.6.3. Reducing power assay ····································································15
2.7. Thin Layer Chromatography ·······························································15
2.8. Determination of DNA damage inhibition················································16
3. Results and discussion ·········································································18
3.1. Batch biodegradation ········································································18
3.1.1. Biomass concentration ····································································19
3.1.2. pH ····························································································21
3.1.3. Production of reducing sugar ····························································23
3.1.4. Antioxidant activity ·······································································26
3.1.4.1. DPPH free radical scavenging activity ···············································26
3.1.4.2. ABTS radical cation decolorization assay ···········································29
3.1.4.3. Reducing power assay ··································································32
3.2. Fed-batch biodegradation ···································································35
3.2.1. Biomass concentration ····································································35
3.2.2. pH ····························································································36
3.2.3. Production of reducing sugar ····························································37
3.2.4. Antioxidant activity ·······································································38
3.2.4.1. DPPH free radical scavenging activity ···············································38
3.2.4.2. ABTS radical cation decolorization assay ···········································39
3.2.4.3. Reducing power assay ··································································39
3.3. Thin Layer Chromatography································································41
3.4. DNA damage inhibition activity····························································43
4. Conclusion·······················································································45
5. Acknowledgements·············································································46
6. References·······················································································48
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