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AKTIVITAS ANTIBAKTERI EKSTRAK BIJI JERUK SIAM (Citrus reticulata) PADA BAKTERI Escherichia coli 大肠杆菌中的暹罗柑橘籽提取物(Citrus reticulata)的抗菌活性
Jurnal Bioteknologi & Biosains Indonesia (JBBI) Pub Date : 2020-11-24 DOI: 10.29122/JBBI.V7I2.4194
Mohammad Arfi Setiawan, Mita Dewi Retnoningrum, Febriyandhi Yahya, Resa Ragil Andika, D. H. A. Sudarni
{"title":"AKTIVITAS ANTIBAKTERI EKSTRAK BIJI JERUK SIAM (Citrus reticulata) PADA BAKTERI Escherichia coli","authors":"Mohammad Arfi Setiawan, Mita Dewi Retnoningrum, Febriyandhi Yahya, Resa Ragil Andika, D. H. A. Sudarni","doi":"10.29122/JBBI.V7I2.4194","DOIUrl":"https://doi.org/10.29122/JBBI.V7I2.4194","url":null,"abstract":"Antibacterial Activity of Citrus seed (Citrus reticulata) Extract on Escherichia coli\u0000Indonesian agriculture provides a resource of medicinal plants whose potential needs to be explored in order to benefit society. One of them is the use of Siam orange seeds (Citrus reticulata) which has the potential for the production of antibacterial compounds. This study aims to test the antibacterial activity of the ethanol and n-hexane extract of orange seeds. The extract was obtained through maceration techniques using ethanol and n-hexane as solvents. The antibacterial activity test of orange seeds against Escherichia coli used the paper disc diffusion method with nutrient agar (NA) media. The concentration of orange seed extract for the determination of MIC (Minimum Inhibitory Concentration) was 0.5, 2, 8, 10, 20 mg mL-1. The results showed that the ethanol and n-hexane extract of orange seeds had antibacterial activity against E. coli. However, the ethanol extract had a higher antibacterial effect than the n-hexane orange seed extract. From the results of this study, it is hoped that the waste of orange seeds will provide beneficial contribution for pharmaceutical development.\u0000Pertanian Indonesia memiliki sumber tanaman obat yang perlu digali potensinya agar bermanfaat bagi masyarakat. Salah satunya pemanfaatan biji jeruk siam (Citrus reticulata) yang berpotensi menghasilkan senyawa antibakteri. Penelitian ini bertujuan untuk menguji aktivitas antibakteri ekstrak etanol dan n-heksana biji jeruk. Ekstrak diperoleh melalui teknik maserasi menggunakan pelarut etanol dan n-heksana. Uji aktivitas antibakteri biji jeruk terhadap Escherichia coli menggunakan metode difusi paper disc dengan media nutrient agar (NA). Konsentrasi ekstrak biji jeruk untuk penentuan MIC (Minimum Inhibitory Concentration) adalah 0,5, 2, 8, 10, 20 mg mL-1. Hasil penelitian menunjukkan bahwa ekstrak etanol dan n-heksana biji jeruk memiliki aktivitas antibakteri terhadap E. coli. Namun, ekstrak etanol memiliki efek antibakteri yang lebih tinggi dibandingkan ekstrak biji jeruk n-heksana. Dari hasil penelitian ini, limbah biji jeruk diharapkan dapat memberikan kontribusi bermanfaat bagi pengembangan farmasi.","PeriodicalId":231498,"journal":{"name":"Jurnal Bioteknologi & Biosains Indonesia (JBBI)","volume":"17 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2020-11-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"128841035","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
AKTIVITAS ANTIFUNGI ASAP CAIR DARI TANDAN KOSONG Elaeis guineensis Jacq.TERHADAP Colletotrichum sp. (WA2) 杀菌剂活性从空碱基中产生的液体烟。反对收藏sp。
Jurnal Bioteknologi & Biosains Indonesia (JBBI) Pub Date : 2020-11-24 DOI: 10.29122/JBBI.V7I2.3582
E. R. P. Wardoyo, Widya Anggraeni, .. Rahmawati, H. A. Oramahi
{"title":"AKTIVITAS ANTIFUNGI ASAP CAIR DARI TANDAN KOSONG Elaeis guineensis Jacq.TERHADAP Colletotrichum sp. (WA2)","authors":"E. R. P. Wardoyo, Widya Anggraeni, .. Rahmawati, H. A. Oramahi","doi":"10.29122/JBBI.V7I2.3582","DOIUrl":"https://doi.org/10.29122/JBBI.V7I2.3582","url":null,"abstract":"Antifungal Activity of Wood Vinegar derived from Oil Palm Empty Bunches against Colletotrichum sp. (WA2)\u0000Colletotrichum sp. is a fungus that causes anthracnose in cayenne pepper (Capsicum frutescens L.).  An alternative natural control for this fungus is using wood vinegar. The aim of this study was to evaluate antifungal properties of wood vinegar from oil palm empty bunches (Elaeis guineensis Jacq.) against Colletotrichum sp. The antifungal test was carried out using the solid dilution method by poisoning food in potato dextrose agar (PDA) media. Colletotrichum sp. used was isolated from red chili which had anthracnose symptoms. This experimental research method used a completely randomized design (CRD) with 9 treatments, namely, negative control (non-liquid smoke), positive control (Dithane M45 at 0.20%), liquid smoke concentration of 0.40; 0.42; 0.44; 0.46; 0.48; 0.50; and 0.52%. Anova test results showed wood vinegar from empty fruit bunches of E. guineensis at concentrations of 0.40; 0.42; 0.44; 0.46 and 0.48% differed significantly from negative control, positive control, and concentrations of 0.50 and 0.52%. The concentration of 0.42% was the minimum inhibitory concentration with an average value of 87.98% inhibition and a very strong activity level. In conclusion, the wood vinegar from E. guineensis can be used to control Colletotrichum sp fungus at an effective concentration of 0.42%.\u0000Colletotrichum sp. merupakan jamur penyebab penyakit antraknosa pada tanaman cabai rawit (Capsicum frutescens L.). Salah satu alternatif pengendalian secara alami terhadap jamur tersebut adalah dengan menggunakan asap cair. Penelitian ini bertujuan untuk mengevaluasi sifat antijamur asap cair dari tandan kosong Elaeis guineensis Jacq (kelapa sawit) terhadap Colletotrichum sp. Uji antijamur dilakukan dengan metode dilusi padat melalui cara poisoning food dalam media potato dextrose agar (PDA). Isolat jamur Colletotrichum sp. yang digunakan merupakan hasil isolasi dari tanaman cabe merah yang bergejala antraknosa. Metode penelitian ini mengunakan rancangan acak lengkap (RAL) dengan 9 perlakuan, yaitu kontrol negatif (tanpa asap cair), kontrol positif (Dithane M45 sebesar 0,20%), konsentrasi asap cair sebesar 0,40; 0,42; 0,44; 0,46; 0,48; 0,50; dan 0,52%. Hasil uji Anova menunjukkan asap cair dari tandan kosong E. guineensis pada konsentrasi 0,40; 0,42; 0,44; 0,46; dan 0,48% berbeda secara signifikan dengan kontrol negatif, kontrol positif dan konsentrasi 0,50 dan 0,52%. Konsentrasi 0,42% merupakan konsentrasi hambat minimum dengan nilai rata-rata penghambatan sebesar 87,98% dan tingkat aktivitas sangat kuat. Dengan demikian dapat disimpulkan bahwa asap cair dari tandan kosong E. guineensis dapat digunakan untuk mengendalikan jamur Colletotrichum sp. pada konsentrasi efektif 0,42%.","PeriodicalId":231498,"journal":{"name":"Jurnal Bioteknologi & Biosains Indonesia (JBBI)","volume":"94 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2020-11-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"121702763","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Front Cover JBBI Vol 6, No 1, June 2019 《JBBI》第6卷第1期封面2019年6月
Jurnal Bioteknologi & Biosains Indonesia (JBBI) Pub Date : 2019-08-06 DOI: 10.29122/jbbi.v6i1.3704
Catur Sriherwanto
{"title":"Front Cover JBBI Vol 6, No 1, June 2019","authors":"Catur Sriherwanto","doi":"10.29122/jbbi.v6i1.3704","DOIUrl":"https://doi.org/10.29122/jbbi.v6i1.3704","url":null,"abstract":"","PeriodicalId":231498,"journal":{"name":"Jurnal Bioteknologi & Biosains Indonesia (JBBI)","volume":"84 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"124126326","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Appendix JBBI Vol 6, No 1, June 2019: Keyword Index and Author Index JBBI第6卷第1期,2019年6月:关键词索引和作者索引
Jurnal Bioteknologi & Biosains Indonesia (JBBI) Pub Date : 2019-08-05 DOI: 10.29122/jbbi.v6i1.3692
Catur Sriherwanto
{"title":"Appendix JBBI Vol 6, No 1, June 2019: Keyword Index and Author Index","authors":"Catur Sriherwanto","doi":"10.29122/jbbi.v6i1.3692","DOIUrl":"https://doi.org/10.29122/jbbi.v6i1.3692","url":null,"abstract":"","PeriodicalId":231498,"journal":{"name":"Jurnal Bioteknologi & Biosains Indonesia (JBBI)","volume":"44 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-08-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"128743875","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Back Cover JBBI Vol 6, No 1, June 2019 封底JBBI第6卷第1期2019年6月
Jurnal Bioteknologi & Biosains Indonesia (JBBI) Pub Date : 2019-07-18 DOI: 10.29122/jbbi.v6i1.3618
Catur Sriherwanto
{"title":"Back Cover JBBI Vol 6, No 1, June 2019","authors":"Catur Sriherwanto","doi":"10.29122/jbbi.v6i1.3618","DOIUrl":"https://doi.org/10.29122/jbbi.v6i1.3618","url":null,"abstract":"","PeriodicalId":231498,"journal":{"name":"Jurnal Bioteknologi & Biosains Indonesia (JBBI)","volume":"32 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-07-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"128124341","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
SKRINING DAN IDENTIFIKASI MIKROBA LIGNINOLITIK PADA PENGOMPOSAN ALAMI TANDAN KOSONG KELAPA SAWIT 对空棕榈油自然堆肥进行筛选和微生物鉴定
Jurnal Bioteknologi & Biosains Indonesia (JBBI) Pub Date : 2019-07-17 DOI: 10.29122/JBBI.V6I1.3237
Bedah Rupaedah, D. Purwoko, Anna Safarrida, Teuku Tajuddin, A. Wahid, Mahmud Sugianto, Imam Sudjai, Agus Suyono
{"title":"SKRINING DAN IDENTIFIKASI MIKROBA LIGNINOLITIK PADA PENGOMPOSAN ALAMI TANDAN KOSONG KELAPA SAWIT","authors":"Bedah Rupaedah, D. Purwoko, Anna Safarrida, Teuku Tajuddin, A. Wahid, Mahmud Sugianto, Imam Sudjai, Agus Suyono","doi":"10.29122/JBBI.V6I1.3237","DOIUrl":"https://doi.org/10.29122/JBBI.V6I1.3237","url":null,"abstract":"Screening and Identification of Ligninolytic Microbes in the Natural Decomposition of Oil Palm Empty Fruit Bunch  ABSTRACTOPEFB (oil palm empty fruit bunch)could potentially be utilized as organic fertilizer or animal feed through composting. Information on microorganisms that play important roles in the natural decomposition of OPEFB is to date not much known yet. This research was aimed to obtain and, subsequently, to molecularly identify lignin-degrading microbial isolates responsible for naturally decomposing OPEFB in the Oil Plant Plantation and Palm Oil Refinery Plant, PTPN VIII Cikasungka, Bogor. Screening for active lignin-degrading isolates was carried out on 17 naturally decomposing OPEFB samples. A total of 19 isolates of fungi and 80 isolates of bacteria were obtained. Ligninolytic activity was measured by Sundman and Nase testing methods. Ligninolytic activity was found on 13 fungal isolates and 15 bacterial isolates. The active isolates were subsequently identified molecularly based on ITS sequence in the ribosome DNA area for fungi and in 16S rRNA genes for bacteria. The results showed that the lignin-degrading microorganisms obtained consisted of 5 bacterial isolates from the genus Bacillus and 3 fungal isolates from the genus Rhizopus and Aspergillus. Keywords: composting, lignin, microbes, OPEFB, 16S rRNA ABSTRAKTKKS (tandan kosong kelapa sawit) berpotensi dimanfaatkan sebagai pupuk organik atau pakan ternak dengan cara pengomposan. Informasi mikroba yang berperan dalam pengomposan alami TKKS hingga saat ini belum banyak diketahui. Penelitian ini bertujuan mendapatkan isolat mikroba pendegradasi lignin dalam pengomposan alami TKKS asal Perkebunan dan Pabrik Pemerasan Kelapa Sawit, PTPN VIII Cikasungka, Bogor, serta mengidentifikasi mikroba tersebut secara molekuler. Skrining mikroba aktif pendegradasi lignin dilakukan terhadap 17 sampel TKKS yang sudah lapuk secara alami. Sebanyak 19 isolat jamur dan 80 isolat bakteri telah dihasilkan. Aktivitas ligninolitik diukur dengan metode pengujian Sundman dan Nase. Isolat jamur yang memiliki aktivitas ligninolitik sebanyak 13 isolat, sedangkan bakteri sebanyak 15 isolat. Isolat-isolat aktif tersebut selanjutnya diidentifikasi secara molekuler berdasarkan pada sekuen ITS di daerah DNA ribosom untuk jamur dan menggunakan gen 16S rRNA untuk bakteri. Hasil menunjukkan bahwa 5 isolat bakteri yang memiliki kemampuan mendegradasi lignin berasal dari genus Bacillus, sedangkan 3 isolat jamur pendegradasi lignin berasal dari genus Rhizopus dan Aspergillus Kata Kunci: lignin, mikroba, pengomposan, TKKS, 16S rRNA ","PeriodicalId":231498,"journal":{"name":"Jurnal Bioteknologi & Biosains Indonesia (JBBI)","volume":"268 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"116396030","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
TRANSFORMASI GENETIK DAN EKSPRESI MUTAN SUCROSE PHOSPHATE SYNTHASE PADA TANAMAN TOMAT
Jurnal Bioteknologi & Biosains Indonesia (JBBI) Pub Date : 2019-07-10 DOI: 10.29122/JBBI.V6I1.3341
Suwinda Fibriani, Inyana Dwi Agustien, Widhi Dyah Sawitri, Bambang Sugiharto
{"title":"TRANSFORMASI GENETIK DAN EKSPRESI MUTAN SUCROSE PHOSPHATE SYNTHASE PADA TANAMAN TOMAT","authors":"Suwinda Fibriani, Inyana Dwi Agustien, Widhi Dyah Sawitri, Bambang Sugiharto","doi":"10.29122/JBBI.V6I1.3341","DOIUrl":"https://doi.org/10.29122/JBBI.V6I1.3341","url":null,"abstract":"Genetic Transformation and Expression of Sucrose Phosphate Synthase Mutant in Tomato Plant ABSTRACTSucrose phosphate synthase (SPS) is a key enzyme responsible for sucrose biosynthesis. In its regulation, SPS activity is modulated by an allosteric effector glucose-6-phosphate (G6P) suggested to have an ability to bind SPS N-terminus domain. To understand the role of N-terminus in regulating SPS, the SPS gene was mutated with the deletion of N-terminus domain (∆N-SPS). The ∆N-SPS gen was transformed into tomato plants with 5% transformation efficiency. Three transgenic tomato plant 4.20, 5.5.1, and 5.10 were obtained and confirmed by PCR analysis. Transgenic tomato expression was characterized by enzymatic analysis. Result showed that the G6P allosteric regulation in transgenic ∆N-SPS had lost and the SPS activity increased by 2-fold compared to non-transgenic plant. This showed that N-terminus domain-deleted SPS could be actively expressed in plant. Keywords: enzyme, genetic transformation, N-terminus domain deletion, sucrose phosphate synthase, tomato ABSTRAKSucrose phosphate synthase (SPS) merupakan enzim kunci yang bertanggung jawab dalam sintesis sukrosa. Dalam regulasinya, aktifitas SPS dipengaruhi oleh alosterik efektor glukosa-6-fosfat (G6P) yang diduga dapat berikatan pada domain N-terminus SPS. Untuk mengetahui peran N-terminus pada regulasi SPS, dilakukan mutasi SPS dengan penghilangan domain N-terminus (∆N-SPS). Gen ∆N-SPS diinsersi pada tanaman tomat melalui transformasi genetik dengan efisiensi transformasi 5%. Tiga tanaman transgenik tomat (event4.20; 5.5.1; dan 5.10) didapatkan dan positif terkonfirmasi melalui analisis PCR. Ekspresi mutan dikarakterisasi melalui analisis enzimatik. Hasil menunjukkan bahwa tanaman tomat transgenik ∆N-SPS tidak dipengaruhi regulasi alosterik G6P dan aktifitas SPS 2 kali lipat lebih tinggi daripada tanaman bukan transgenik. Ini menunjukkan bahwa SPS dengan delesi domain N-terminus dapat terekspresi aktif pada tanaman.  Kata Kunci: delesi domain N-terminus, enzim, sucrose phosphate synthase, tomat, transformasi genetik ","PeriodicalId":231498,"journal":{"name":"Jurnal Bioteknologi & Biosains Indonesia (JBBI)","volume":"57 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"116468914","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
PERBANDINGAN TIGA KIT EKSTRAKSI RNA UNTUK ANALISIS TRANSKRIPTOMIKA PADA KELAPA SAWIT (Elaeis guineensis Jacq.)
Jurnal Bioteknologi & Biosains Indonesia (JBBI) Pub Date : 2019-07-09 DOI: 10.29122/JBBI.V6I1.3372
Siti Zulaeha, Devit Purwoko, Imam Civi Cartealy, Teuku Tajuddin, .. Karyanti, H. Khairiyah
{"title":"PERBANDINGAN TIGA KIT EKSTRAKSI RNA UNTUK ANALISIS TRANSKRIPTOMIKA PADA KELAPA SAWIT (Elaeis guineensis Jacq.)","authors":"Siti Zulaeha, Devit Purwoko, Imam Civi Cartealy, Teuku Tajuddin, .. Karyanti, H. Khairiyah","doi":"10.29122/JBBI.V6I1.3372","DOIUrl":"https://doi.org/10.29122/JBBI.V6I1.3372","url":null,"abstract":"Comparison of Three RNA Extraction Kits for Transcriptome Analysis of Oil Palm (Elaeis guineensis Jacq.) ABSTRACTObtaining high-quality RNA is very important at an early stage of molecular biology research. To isolate RNA, high skill and caution are required in following laboratory procedures because RNA is easily degraded, especially samples from plant tissue culture. One of the parameters used to check the total RNA quality is RIN (RNA Integrity Number). The aim of this study was to obtain RNA extraction methods on oil palm leaves, callus and somatic embryos that were of good quality and high concentrations for transcriptomic analysis. RNA extraction was carried out using Plant RNA PureLink (Ambion), Genezol RNA Extraction (Geneaid) and RibospinTM Plant (Geneall) kit methods. The results showed that oil palm leaf, callus and somatic embryo RNA were successfully extracted using the RibospinTM (Geneall) kit. Based on the total RNA number of more than 4 μg and the RIN value of more than 7, the extracted RNA could be used in RNA sequencing for transcriptomic analysis. Keywords: callus, oil palm, RNA analysis, RNA quality, somatic embryo ABSTRAKMenghasilkan RNA berkualitas tinggi sangatlah penting pada tahap awal penelitian biologi molekuler. Untuk mengisolasi RNA diperlukan keterampilan dan kehati-hatian tinggi dalam mengikuti prosedur di laboratorium karena RNA lebih mudah terdegradasi, khususnya sampel hasil kultur jaringan tanaman. Salah satu parameter yang digunakan pada pengecekan kualitas RNA total adalah RIN (RNA Integrity Number). Penelitian bertujuan mendapatkan metode ekstraksi RNA pada daun, kalus dan embrio somatik kelapa sawit yang berkualitas baik dan memiliki konsentrasi tinggi untuk analisa transkriptomika.  Ekstraksi RNA dilakukan menggunakan metode kit Plant RNA PureLink (Ambion), Genezol RNA Extraction (Geneaid) dan RibospinTM Plant (Geneall). Hasil menunjukkan bahwa RNA daun, kalus dan embrio somatik kelapa sawit telah berhasil diekstraksi dengan menggunakan kit RibospinTM (Geneall). RNA hasil ekstraksi tersebut dapat digunakan untuk sekuensing RNA dengan tujuan analisis transkriptomika, dilihat dari jumlah total RNA yang lebih dari 4 μg dan nilai RIN lebih dari 7. Kata Kunci: analisis RNA, embrio somatic, kalus, kelapa sawit, kualitas RNA ","PeriodicalId":231498,"journal":{"name":"Jurnal Bioteknologi & Biosains Indonesia (JBBI)","volume":"21 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-07-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"115484089","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
PENGARUH TEKNIK PENGAPUNGAN HAYATI MELALUI FERMENTASI Rhizopus sp. TERHADAP KANDUNGAN NUTRISI PAKAN IKAN APUNG 生物过滤技术对浮鱼营养丰富的影响
Jurnal Bioteknologi & Biosains Indonesia (JBBI) Pub Date : 2019-07-08 DOI: 10.29122/JBBI.V6I1.3477
S. A. Paramadini, Catur Sriherwanto, Nurlaila, I. Suja’i, M. Annisa
{"title":"PENGARUH TEKNIK PENGAPUNGAN HAYATI MELALUI FERMENTASI Rhizopus sp. TERHADAP KANDUNGAN NUTRISI PAKAN IKAN APUNG","authors":"S. A. Paramadini, Catur Sriherwanto, Nurlaila, I. Suja’i, M. Annisa","doi":"10.29122/JBBI.V6I1.3477","DOIUrl":"https://doi.org/10.29122/JBBI.V6I1.3477","url":null,"abstract":"Influence of Biofloatation Technique through Rhizopus sp. Fermentation on the Nutritional Quality of the Floating Fish FeedABSTRACTSolid fermentation using the mold Rhizopus has been used as an alternative method to improve the physical quality of fish feed, namely stability in water and floatability. Although the fermented fish feed produced had been shown previously to have better stability in water and floatability, the effect of the fermentation on the fish feed nutrition has not yet been known. This study aimed to determine the effect of solid fermentation using the mold Rhizopus sp. on the nutrient content of the fermented feed. In addition, the effect of adding tapioca as much as 0, 1, 2, 3, and 4 g to the dry weight loss and density of the fermented feed was investigated. The results showed that the fermented feed contained higher levels of ash and protein than that before fermentation. The addition of tapioca up to 4 g had no significat effect (p>0.01) on the dry weight loss of the fermented feed, but tended to increase its density compared to those without tapioca addition.Keywords: density, fermentation, fish feed, nutrition, Rhizopus ABSTRAKFermentasi padat menggunakan kapang Rhizopus telah digunakan sebagai metode alternatif untuk memperbaiki kualitas fisik pakan ikan, yakni stabilitas dalam air dan daya apung. Meskipun pakan ikan fermentasi yang dihasilkan sebelumnya sudah dibuktikan memiliki stabilitas dalam air dan daya apung yang lebih baik, namun pengaruh fermentasi terhadap nutrisi pakan ikan tersebut belumlah diketahui. Penelitian ini bertujuan mengetahui pengaruh fermentasi padat menggunakan kapang Rhizopus sp. terhadap kandungan nutrisi pakan fermentasi, dan pengaruh penambahan tapioka sebanyak 0, 1, 2, 3, dan 4 g terhadap kehilangan berat kering dan mass jenis pakan hasil fermentasi. Hasilnya menunjukkan bahwa pakan fermentasi mengandung kadar abu dan protein lebih tinggi dibandingkan sebelum difermentasi. Penambahan tapioka hingga 4 g tidak berpengaruh nyata (p>0,01) pada kehilangan berat kering pakan fermentasi, namun cenderung meningkatkan massa jenis dibandingkan tanpa penambahan tapioka.Kata kunci: fermentasi, massa jenis, nutrisi, pakan ikan, Rhizopus","PeriodicalId":231498,"journal":{"name":"Jurnal Bioteknologi & Biosains Indonesia (JBBI)","volume":"9 9 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"116868018","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
PENGARUH VARIASI KONSENTRASI METANOL DAN LAMA INDUKSI TERHADAP EKSPRESI PROINSULIN OLEH Pichia pastoris SECARA INTRASELULER 皮基亚牧师在细胞内对甲醇浓度的变化和长期诱导黄黄素表达的影响
Jurnal Bioteknologi & Biosains Indonesia (JBBI) Pub Date : 2019-07-03 DOI: 10.29122/JBBI.V6I1.3176
Efrida Martius, Andree Triyadi, D. Y. Sofia, Anis Herliyati Mahsunah
{"title":"PENGARUH VARIASI KONSENTRASI METANOL DAN LAMA INDUKSI TERHADAP EKSPRESI PROINSULIN OLEH Pichia pastoris SECARA INTRASELULER","authors":"Efrida Martius, Andree Triyadi, D. Y. Sofia, Anis Herliyati Mahsunah","doi":"10.29122/JBBI.V6I1.3176","DOIUrl":"https://doi.org/10.29122/JBBI.V6I1.3176","url":null,"abstract":"The Effects of Variation in Methanol Concentration and Induction Time on Intracellular Proinsulin Expression by Pichia pastoris ABSTRACTDiabetes is a metabolic disorder characterized by hyperglycemia. There were 215 million diabetic patients in 2014 and the number is expected to rise in 2040. Generally, insulin is used to treat diabetic patients. Insulin production by recombinant technology has been done, though still inefficient, by using E. coli and S. cerevisiae expression system. Another alternative expression system is methylotrophic yeast Pichia pastoris. In this research, proinsulin has been expressed by P. pastoris intracellularly. P. pastoris strains used in this research were X33, GS115, and KM71H. All recombinant strains were MutS. Best cultivation media was BMGY. Proinsulin expression was observed at 25°C. Pichia pastoris strain that expressed proinsulin best was GS115-PI. It was supported by PCR in which the strain GS115-PI gave 504 bp-sized bands. Based on proinsulin formation time, the final methanol concentration of 0.5% in 72 hours was found to be the best treatment.Keywords: BMGY, methanol, phenotype, Pichia pastoris, proinsulin ABSTRAKDiabetes melitus merupakan kelainan yang ditandai dengan hiperglikemia. Penderita diabetes pada tahun 2014 di dunia mencapai 215 juta dan diperkirakan akan meningkat pada tahun 2040. Umumnya penderita diabetes diberi pengobatan insulin sehingga menunjukkan akan ada peningkatan kebutuhan insulin. Produksi insulin dengan teknologi DNA rekombinan telah dilakukan dengan menggunakan sistem ekspresi E. coli dan S. cerevisiae namun masih belum efisien. Sistem alternatif lain adalah ragi metilotropik Pichia pastoris. Dalam penelitian ini dilakukan ekspresi proinsulin dari P. pastoris secara intraseluler. Galur P. pastoris yang digunakan dalam penelitian ini adalah X33, GS115, dan KM71H. Semua galur rekombinan adalah MutS. Media tumbuh terbaik adalah BMGY. Ekspresi proinsulin terlihat pada suhu 25°C. Hasil PCR menunjukkan bahwa galur GS115-PI yang dapat menghasilkan pita amplikon berukuran 504 bp. Hasil PCR ini dibuktikan oleh hasil seleksi galur yang menunjukkan bahwa galur GS115-PI dapat mengekspresi proinsulin dibandingkan galur lainnya. Berdasarkan kecepatan pembentukan pita protein proinsulin, variasi konsentrasi akhir metanol 0,5% dengan lama induksi 72 jam merupakan perlakuan terbaik.Kata Kunci: BMGY, fenotipe, metanol, Pichia pastoris, proinsulin","PeriodicalId":231498,"journal":{"name":"Jurnal Bioteknologi & Biosains Indonesia (JBBI)","volume":"14 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"114574609","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
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