Isolasi Identifikasi Bakteri Penghasil Xilanase Serta Karakterisasi Enzimnya

Xylanase is an extracellular enzyme produced bymicroorganisms. This enzyme is able to hydrolise xylane(hemicellulose) to produce xylooligosaccharide and xylose.Thermoalkaliphilic xylanase is an agent that can be used asa substitute in the pulp whitening process instead of chlorine.A study was done to isolate, identificate of bacteria andcharacterize xylanase. The isolation of xylanase producingbacteria has been done from soil and waste of starch industry.Colonies which produced clearing zone were presumedas xylanolytic bacteria and chosen for further screening.Identification of potential isolate in xylanase production wasdone using 16S ribosomal RNA sequencing. Isolate Bacilluspumilus RXA-III5 originated from lime or alkaline soil wasmore potential isolate in xylanase production than other 24isolates. Precipitation of xylanase, that was done usingammonium sulphate followed by dialyzes produced xylanaseof a higher specific activity (267.1 U.mg-1) than that usingacetone (131.1 U.mg-1) and ethanol (186.65 U.mg-1). Xylanasewas done at purification produced three fractions of xylanase.Xylanase characteristics consist of pH and temperature(9 and 50oC), Km and Vmaks value 6 mg.ml-1 and 0.2mol.minute-1, respectively. The Fe2+ was the strongest activetorand Mg2+ was the strongest inhibitor activity. This enzymewas detected as a cellulose-free xylanase. Xylanase is aprospective agent for bio-bleaching of paper

Potency of (Poly) Acrylic/Carboxymethyl Starch-Chitosan Biohydrogel for Curcumin Oral Delivery Matrix

Objective: Biohydrogel has gathered great interest in the pharmaceuticals field. This natural polymers were biodegradable, non-toxic, biocompatible, and its specific ability to response environment change can be considered for the controlled released matric of bioactive compound. In this study, the biohydrogel was synthesized by graft-copolymerization of acrylic acid onto carboxymethyl starch (CMS) and chitosan. The objective of this research was to determine the effect of CMS-chitosan ratio on the biohydrogel characteristic. Methods: The acrylic acid was grafted on to the backbone (3:1) by using cerric ammonium nitrate as the inisiator. A standarded curcumin was applied to test the binding potency of matrix. Results: A higher CMS ratio in the polymer mixture (4:1) revealed the highest swelling power (16.9 w/w) and percentage of curcumin absorption (17.34%). All the samples have the pH-responsive swelling properties, with the swelling trend was observed in the order of distilled water > HCl solution > phospathe buffer solution. FTIR spectra and SEM micrographs has confirmed the graft-copolymerization of PAA/CMSCs biohydrogel by describing the appearance of peak around 1600 cm-1 and the morphology of granula structure, respectively. Conclusion: The graft-copolymerization of acrylic acid onto the two anionic natural polymer by cerric ammonium nitrate as the initiator has resulted a pH-dependent swelling biohydrogel, and it has the ability to deliver curcumin in stomach-targeted system

Isolasi Identifikasi Bakteri Penghasil Xilanase serta Karakterisasi Enzimnya

Xylanase is an extracellular enzyme produced bymicroorganisms. This enzyme is able to hydrolise xylane(hemicellulose) to produce xylooligosaccharide and xylose.Thermoalkaliphilic xylanase is an agent that can be used asa substitute in the pulp whitening process instead of chlorine.A study was done to isolate, identificate of bacteria andcharacterize xylanase. The isolation of xylanase producingbacteria has been done from soil and waste of starch industry.Colonies which produced clearing zone were presumedas xylanolytic bacteria and chosen for further screening.Identification of potential isolate in xylanase production wasdone using 16S ribosomal RNA sequencing. Isolate Bacilluspumilus RXA-III5 originated from lime or alkaline soil wasmore potential isolate in xylanase production than other 24isolates. Precipitation of xylanase, that was done usingammonium sulphate followed by dialyzes produced xylanaseof a higher specific activity (267.1 U.mg-1) than that usingacetone (131.1 U.mg-1) and ethanol (186.65 U.mg-1). Xylanasewas done at purification produced three fractions of xylanase.Xylanase characteristics consist of pH and temperature(9 and 50oC), Km and Vmaks value 6 mg.ml-1 and 0.2mol.minute-1, respectively. The Fe2+ was the strongest activetorand Mg2+ was the strongest inhibitor activity. This enzymewas detected as a cellulose-free xylanase. Xylanase is aprospective agent for bio-bleaching of paper

Produksi Bioetanol dari Hidrolisat Asam Tepung Ubi Kayu dengan Kultur Campuran Trichoderma viride dan Saccharomyces cerevisiae

The objective of this research was to produce bioethanol from acid hydrolysate cassava flour with mix cultured Trichoderma viride and Saccharomyces cerevisiae. The hydrolysis of cassava flour to glucose was conducted by 0.4 M sulfuric acid using autoclave at 121°C, pressure at 1 atm for 10 min. The fermentation were performed in batch system for 96 hours in 30°C. Mixed culture of T. viride and S. cerevisiae in the fermentation process of acid hydrolysate carried out in two methode that is gradually and simultaneously. The results showed the acid hydrolyzate of cassava flour has a total sugar concentration of 38.93 ± 8.09% (w/v) and reducing sugar concentration of 22.04 ± 4.31% (w/v) . In the bioethanol production process shows that the bioethanol concentration 6.77 ± 1.23% (v/v), yield 27,97% (v/w) and fermentation effciency 59,01% of the theoretical value was achieved using gradually addition of mixed culture, while simultaneously addition of mixed culture was produced ethanol concentration 4.96 ± 0.39%(v/v), yield 19.85% (v/w) and fermentation effciency 62.72% of the theoretical value.ABSTRAKTujuan dari penelitian ini adalah untuk memproduksi bioetanol dari hidrolisat asam tepung ubi kayu dengan menggunakan kultur campuran Trichoderma viride and Saccharomyces cerevisiae. Hidrolisis tepung ubi kayu untuk menghasilkan glukosa dilakukan dengan menggunakan H2SO4 0.4M, pada suhu 121°C, tekanan 1 atm selama 10 menit. Proses fermentasi dilaksanakan secara batch selama 96 jam pada suhu 30°C. Pencampuran kultur T. viride dan S. cerevisiae pada proses fermentasi hidrolisat asam dilakukan dalam dua metode yaitu secara bertahap dan secara simultan. Hasil penelitian menunjukkan hidrolisat asam tepung ubi kayu mempunyai konsentrasi total gula 38,93 ± 8,09% (b/v) dan konsentrasi gula reduksi 22,04 ± 4,31% (b/v). Pada proses produksi bioetanol menunjukan bahwa dengan pencampuran kultur secara bertahap menghasilkan konsentrasi bioetanol 6,77 ± 1,23% (v/v), rendemen 27,97% (v/w) dan efisiensi fermentasi 59,01% dari perolehan bioetanol secara teoritis, sedangkan dengan pencampuran kultur secara simultan menghasilkan konsentrasi bioetanol 4,96 ± 0,39%(v/v), rendemen 19,85% (v/w) dan efisiensi fermentasi 62,72% dari perolehan bioetanol secara teoritis

KARAKTERISASI GEN PENYANDI PEDIOSIN PAF-11 PADA Pediococcus Acidilactici F-11 [Characterization of the Pediocin PaF-11 Encoding Gene in Pediococcus Acidilactici F-11]

Pediocin PaF-11 is a ribosomally synthesized antimicrobial peptide produced by Pediococcus acidilactici F-11. The objectives of this research is to find out the location and the nucleotide sequence of gene, which is involved in the production of pediocin PaF-11. Results showed that the pediocin PaF-11 from the cured cell of P. acidilactici F-11 loss the activity, suggested that the pediocin PaF-11 gene was carried in the plasmid. Agarose gel electrophoresis of P. acidilactici F-11 plasmid DNA with marker λDNA/HindIII showed that pediocin PaF-11 gene was carried in 12 kb plasmid. Amplification pediocin PaF-11 gene from P. acidilactici F-11 showed that uncured P.acidilactici F-11 culture contain plasmid DNA, indicated by amplification of the papA gene (256 bp). Cured P. acidilactici F-11 culture, plasmid eliminated, indicted by no aplicon DNA detected. This result also suggested that pediocin PaF-11 gene in P. acidilactici F-11 was carried in plasmid. Nucleotide of pediocin PaF-11 encoding gene was sequenced The alignment of that nucleotide sequence showed that pediocin PaF-11 encoding gene have the same sequence with pediocin PA.1 encoding gene in P. acidilactici PAC1.0 and P. acidilactici K10 and pediocin AcH encoding gene in P. acidilactici LB 42-923 and P .parvulus ATO77, and pediocin CP2 in P. acidilactici MTCC 5101

Optimasi Waktu Fermentasi Produksi Bioetanol Dari Dedak Sorghum Manis (Sorghum Bicolor L) Melalui Proses Enzimatis

Salah satu energi baru terbarukan (EBT) yang potensial untuk dikembangkan adalah penggunaan bioetanol. Bioetanol merupakan salah satu EBT yang banyak dipertimbangkan sebagai bahan bakar pensubtitusi minyak bumi. Sorgum merupakan tanaman yang dapat dijadikan sebagai bahan baku untuk produksi bioetanol. Tujuan penelitian ini yaitu untuk memperoleh konsentrasi enzim terbaik saat hidrolisis dan waktu fermentasi yang optimum pada produksi bioetanol dari dedak sorgum manis. Penelitian dilaksanakan di Laboratorium Balai Besar Penelitian dan Pengembangan Pascapanen Pertanian, Bogor pada bulan Januari-Mei 2016. Bahan-bahan yang digunakan meliputi dedak sorgum manis, enzim amilase, enzim glukoamilase dan Saccharomyces cereviseae. Pada penelitian ini terdapat tiga tahapan kegiatan, yang meliputi: 1). Karakteristik bahan baku, 2). Optimasi hidrolisis enzimatis terhadap produksi gula dari dedak sorgum 3). Optimasi pengaruh perlakuan penambahan konsentrasi enzim (α-amilase dan glukoamilase) dan lama fermentasi terhadap produksi bioetanol dari dedak sorgum. Hasil penelitian menunjukkan bahwa dedak sorgum manis dapat digunakan sebagai bahan baku pembuatan bioetanol dengan waktu fermentasi optimum selama 48 jam dengan penambahan konsentrasi enzim α-amilase : glukoamilase (0,5 : 1,5) ml/kg dengan hasil rendemen sebanyak 20,88%

KARAKTERISASI GEN PENYANDI PEDIOSIN PAF-11 PADA Pediococcus acidilactici F-11

Pediocin PaF-11 is a ribosomally synthesized antimicrobial peptide produced by Pediococcus acidilactici F-11. The objectives of this research is to find out the location and the nucleotide sequence of gene, which is involved in the production of pediocin PaF-11. Results showed that the pediocin PaF-11 from the cured cell of P. acidilactici F-11 loss the activity, suggested that the pediocin PaF-11 gene was carried in the plasmid. Agarose gel electrophoresis of P. acidilactici F-11 plasmid DNA with marker λDNA/HindIII showed that pediocin PaF-11 gene was carried in 12 kb plasmid. Amplification pediocin PaF-11 gene from P. acidilactici F-11 showed that uncured P.acidilactici F-11 culture contain plasmid DNA, indicated by amplification of the papA gene (256 bp). Cured P. acidilactici F-11 culture, plasmid eliminated, indicted by no aplicon DNA detected. This result also suggested that pediocin PaF-11 gene in P. acidilactici F-11 was carried in plasmid. Nucleotide of pediocin PaF-11 encoding gene was sequenced The alignment of that nucleotide sequence showed that pediocin PaF-11 encoding gene have the same sequence with pediocin PA.1 encoding gene in P. acidilactici PAC1.0 and P. acidilactici K10 and pediocin AcH encoding gene in P. acidilactici LB 42-923 and P .parvulus ATO77, and pediocin CP2 in P. acidilactici MTCC 5101