Serangkaian penelitian dilakukan untuk menggantikan bungkil kedelai (SBM) dengan bungkil inti sawit (PKC) dalam ransum ayam petelur. Tahap pertama dilakukan untuk meningkatkan kandungan protein dan asam amino BIS melalui proses fermentasi dan dilanjutkan dengan penambahan enzim untuk meningkatkan kecernaan asam amino. Selanjutnya dilakukan uji biologis untuk mengetahui efektifitas PKC yang sudah difermentasi (FPKC) dan ditambahkan enzim (EFPKC) untuk menggantikan SBM didalam ransum ayam petelur. Nilai energy (AME) dari PKC, FPKC dan EFPKC diukur dengan menggunakan ayam broiler dan dilanjutkan dengan pengukuran nilai asam amino tercerna pada ileal (IAAD). Nilai AME dan IAAD dari EFPKC kemudian digunakan untuk meramu ransum penelitian. Ransum diberikan pada ayam petelur umur 51 minggu selama 8 minggu. Lima (5) jenis ransum disusun dengan kandungan gizi yang sama, tetapi SBM diganti dengan EFPKC secara bertingkat. Ransum perlakuan terdiri dari 1. Kontrol (tanpa EFPKC), 2. 25% SBM dalam ransum Kontrol diganti dengan EFPKC, 3. 50% SBM dalam ransum Kontrol diganti dengan EFPKC, 4. 75% SBM dalam ransum Kontrol diganti dengan EFPKC and 5. 100% of SBM dalam ransum Kontrol diganti dengan EFPKC. Setiap ransum perlakuan diberikan pada 24 ekor ayam (6 ulangan, 4 ekor/ulangan). Hasil penelitian menunjukkan bahwa fermentasi PKC meningkatkan protein kasar dan asam amino, kecuali threonin dan arginin, tetapi menurunkan AME. Penambahan enzim pada FPKC meningkatkan nilai IAAD. Akan tetapi hanya enzim BS4 yang dapat meningkatkan nilai AME pada EFPKC. Uji biologis menunjukkan bahwa sekitar 25 hingga 50% bungkil kedelai didalam ransum dapat diganti dengan bungkil inti sawit yang sudah difermentasi dan ditambahkan enzim tanpa meyebabkan gangguan yang berarti pada performan ayam petelur.
The use of palm kernel cake (PKC) and palm oil mill effluent (POME), substances from palm oil factory wastes, for monogastric is limited by their high cellulose and mannan contents. Hydrolytic enzymes have been supplemented to increase the nutrient digestibility. The maximal digestibility was obtained in the synergistic action of all enzyme components including B-D-endoglucanase (CMCase), B-D-glucosidase, B-D-mannanase, p-D-mannosidase, and oc-Dgalactosidase. Two kinds of enzymes produced by Eupenicillium javanicum and Aspergillus niger NRRL 337 on the submerged culture containing 3% coconut meal were selected to hydrolyze PKC or dry POME. Enzyme from E. javanicum contained higher CMCase, B-D-mannanase, and a-D-galactosidase activities, while that from A. niger NRRL 337 contained more p-D-glucosidase and p-D-mannosidase activities. Saccharification (hydrolytic) activities of enzyme mixtures on PKC and POME were determined at pH 5.0, the optimal pH for p-D-mannanase from E. javanicum, and at 5.4 the optimal pH for a-D-galactosidase from E. javanicum and P-D-glucosidase from A. niger NRRL 337. The enzyme proportions of E. javanicum and A. niger NRRL 337 were 100 : 0, 80 : 20, 60 : 40, 40 : 60, and 0 : 100%. The highest Saccharification activity on both substrates was observed on the mixture of 80% A. niger NRRL 337. The pH levels did not significantly affect Saccharification activity. Fiber components in PKC were more digestable than in POME. Further analysis on the reducing sugar components using thin layer chromatography showed that more monomers were produced in the 60 or 80% of A. niger NRRL 337. The glycosidases of A. niger NRRL 337 played more important role in the Saccharification activity.
Foot rot disease of black pepper caused by Phytophthora capsici had been reported in Batangas and Laguna, Philippines. The plant was recovered following the application of crop residue (organic substrate) and intercropping with other crops. This study was aimed to isolate, identify, and determine the soil mycoflora from the rhizosphere of black pepper grown on various cropping patterns in Batangas and Laguna. Antagonistic activity of mycoflora isolates was tested against P. capsici using dual culture technique. The result showed that 149 colonies of soil mycoflora isolated were belonging to 14 genera; three of them, i.e. Penicillium, Paecilomyces and Aspergillus, were the most dominant. All of the mycoflora isolates were able to inhibit the growth of the pathogen. Eighteen of them were the most promising antagonists, based on their inhibition growth of more than 60%. It is suggested that antagonistic mechanism of Mucor isolate (1001), Trichoderma (125, 170, 171, 179, 180, 181), Gliocladium (109), Cunninghamella (165, 168), Mortierella (177), and Aspergillus (106) was space competitor (competition for nutrient) since they rapidly overgrew the pathogen. Aspergillus (67, 79, 81, 83, 108, and 202) isolates inhibited the pathogen apparently by producing antibiotic, whereas Trichoderma (125, 170, 171, 179, 180, and 181) isolates were able to penetrate the hyphae of the pathogen. The organic matter percentage in the soil was significantly correlated with the number of antagonistic mycoflora in rhizosphere (R2 = 0.1094), but the cropping pattern wPoultry are not able to digest fiber in the diet. Hydrolytic enzymes including cellulases and hemicellulases have been used as poultry feed supplement. Termites (Glyptotermes montanus) have the ability to digest wood that contains high fiber. The purpose of this experiment was to identify the cellulase and hemicellulase of termite extract. The hydrolytic (saccharification) activity of the termite extract on feedstuffs was then evaluated. It contained high endo-β-D-1,4-glucanase (CMCase) activity, but the activities of avicelase, β-D-1,4-mannanase, β- D-1,4-xylanase, and β-D-1,4-glucosidase were very low. The activities of the enzymes were higher in the fresh extract than those extracted after drying at 40oC with blower oven. CMCase (as cellulase), β-D-1,4-mannanase (as hemicellulase), and β-D- 1,4-glucosidase (as glycosidase) were reevaluated further to determine the optimum pH and temperatures for maximum activities. The optimum pH for CMCase, β-D-1,4-mannanase, and β-D-1,4-glucosidase were 6.2, 5.0, and 5.8 respectively, while the optimum temperatures were 45-50oC, 50-55oC, and 42-45oC, respectively. The enzyme mixture or cocktail was more appropriate in digesting feedstuffs with high lignocellulose (fiber) such as rice bran and pollard than feedstuffs with more soluble starch such as soybean and corn meals. The extracted enzyme could be immobilized with pollard, but CMCase recovery was low (28.6%), while β-D-1,4-mannanase and β-D-1,4-glucosidase recoveries were 89.2% and 272.9%, respectively. Termite extract contained enzyme cocktails of lignocellulases that potentially be used as feed supplement. However, its use is limited by its low activity.as negatively correlated. This study suggests that organic matter increased antagonistic mycoflora in black pepper rhizosphere, which will reduce severity of the disease.
Bacillus pumilus PU4-2 produces xylanase (β-1,4-D-xylan xylanohydrolase; EC 3.2.1.8) in wheat pollard with high activity. Water and NaOH-soaked pollard were used in this research to enhance the production of assayable enzyme. Enzyme activity was produced in minimal media containing 3% w/v untreated or water or NaOH-soaked pollards in 250 ml flasks incubated on shaker incubator at 30°C and 150 rpm for 36 h. The production was also compared to untreated oatmeal known as an inducer substrate. The highest xylanase activity was obtained by using untreated pollard as a sole carbon source. The enzyme activity was 157 U ml -1 with specific activity at 718 U mg -1 . Xylanase production using different soaking time for water pretreated pollard also confirmed that untreated pollard was the best inducer. The production was not influenced by different water soaking times used to remove reducing sugar. Although pretreatment decreased the reducing sugar, the reduction did not enhance assayable enzyme levels. The production was best induced by the soluble oligosaccharides of untreated pollard. We conclude that B. pumilus PU4-2 was able to produce xylanase with reducing sugar content up to 660 ppm present in production medium. With this reducing sugar level, repression of enzyme production was not detected in the production medium.
Foot rot disease of black pepper caused by Phytophthora capsici had been reported in Batangas and Laguna, Philippines. The plant was recovered following the application of crop residue (organic substrate) and intercropping with other crops. This study was aimed to isolate, identify, and determine the soil mycoflora from the rhizosphere of black pepper grown on various cropping patterns in Batangas and Laguna. Antagonistic activity of mycoflora isolates was tested against P. capsici using dual culture technique. The result showed that 149 colonies of soil mycoflora isolated were belonging to 14 genera; three of them, i.e. Penicillium, Paecilomyces and Aspergillus, were the most dominant. All of the mycoflora isolates were able to inhibit the growth of the pathogen. Eighteen of them were the most promising antagonists, based on their inhibition growth of more than 60%. It is suggested that antagonistic mechanism of Mucor isolate (1001), Trichoderma (125, 170, 171, 179, 180, 181), Gliocladium (109), Cunninghamella (165, 168), Mortierella (177), and Aspergillus (106) was space competitor (competition for nutrient) since they rapidly overgrew the pathogen. Aspergillus (67, 79, 81, 83, 108, and 202) isolates inhibited the pathogen apparently by producing antibiotic, whereas Trichoderma (125, 170, 171, 179, 180, and 181) isolates were able to penetrate the hyphae of the pathogen. The organic matter percentage in the soil was significantly correlated with the number of antagonistic mycoflora in rhizosphere (R2 = 0.1094), but the cropping pattern wPoultry are not able to digest fiber in the diet. Hydrolytic enzymes including cellulases and hemicellulases have been used as poultry feed supplement. Termites (Glyptotermes montanus) have the ability to digest wood that contains high fiber. The purpose of this experiment was to identify the cellulase and hemicellulase of termite extract. The hydrolytic (saccharification) activity of the termite extract on feedstuffs was then evaluated. It contained high endo-β-D-1,4-glucanase (CMCase) activity, but the activities of avicelase, β-D-1,4-mannanase, β- D-1,4-xylanase, and β-D-1,4-glucosidase were very low. The activities of the enzymes were higher in the fresh extract than those extracted after drying at 40oC with blower oven. CMCase (as cellulase), β-D-1,4-mannanase (as hemicellulase), and β-D- 1,4-glucosidase (as glycosidase) were reevaluated further to determine the optimum pH and temperatures for maximum activities. The optimum pH for CMCase, β-D-1,4-mannanase, and β-D-1,4-glucosidase were 6.2, 5.0, and 5.8 respectively, while the optimum temperatures were 45-50oC, 50-55oC, and 42-45oC, respectively. The enzyme mixture or cocktail was more appropriate in digesting feedstuffs with high lignocellulose (fiber) such as rice bran and pollard than feedstuffs with more soluble starch such as soybean and corn meals. The extracted enzyme could be immobilized with pollard, but CMCase recovery was low (28.6%), while β-D-1,4-mannanase and β-D-1,4-glucosidase recoveries were 89.2% and 272.9%, respectively. Termite extract contained enzyme cocktails of lignocellulases that potentially be used as feed supplement. However, its use is limited by its low activity.as negatively correlated. This study suggests that organic matter increased antagonistic mycoflora in black pepper rhizosphere, which will reduce severity of the disease.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.