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"L-glutaminase (L-glutamine amidohydrolase, EC 3.5.1.2) telah menarik perhatian para peneliti karena manfaatnya dalam industri farmasi dan makanan. Bakteri laut merupakan sumber penghasil L-glutaminase yang paling diminati, terutama untuk memperoleh L-glutaminase yang tahan garam. Pada penelitian ini telah dilakukan penapisan dan karakterisasi L-glutaminase ekstraselular yang dihasilkan oleh bakteri laut dari perairan Sangihe-Talaud, Sulawesi Utara, Indonesia. Penapisan L-glutaminase secara kualitatif menggunakan media cair (Padma, et.al., 2009) dan metode pengukuran aktivitas L-glutaminase dilakukan secara spektrofotometri berdasarkan metode Imada, et.al (1973). Identifikasi isolat murni dengan aktivitas L-glutaminase paling tinggi dilakukan menggunakan sekuensing gen 16S rRNA. Terdapat 7 isolat menunjukkan hasil positif L-glutaminase, satu diantaranya dengan aktivitas 147,99 U/L atau setara dengan aktivitas spesifik 62,32 Unit/mg dipilih untuk diidentifikasi lebih lanjut. Hasil sekuensing gen 16S rRNA isolat bakteri menunjukkan kemiripan 96% dengan Pseudomonas aeruginosa strain CG-T8. Parameter fisika yang mempengaruhi produksi L-glutaminase menunjukkan produksi optimum pada suhu 30 0C, kecepatan rotasi 100 rpm, pH media 6, dan konsentrasi starter inokulum 5%. Karakterisasi aktivitas L-glutaminase ekstraselular dari Pseudomonas aeruginosa strain CG-T8 (isolat II.1) menunjukkan kondisi optimum aktivitas enzim pada suhu 37-45 0C, dan pH 7. Aktivitas enzim stabil pada penambahan larutan NaCl hingga 8% dan aktivitasnya mulai berkurang pada penambahan larutan NaCl 16% dan 20% dengan aktivitas relatif berturut-turut mencapai 79,00% dan 74,22%. Pengaruh penambahan ion-ion logam seperti Mn2+, Mg2+, dan Co2+ menunjukkan kenaikan aktivitas, sedangkan pada penambahan ion logam Zn2+, Fe3+, dan Ca2+ aktivitas enzim menurun. Bobot molekul L-glutaminase berkisar 42 kDa dan 145 kDa.

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L-glutaminase (L-glutamine amidohydrolase, EC 3.5.1.2) has attracted much attention with respect to proposed applications in both pharmaceuticals and food industries. Salt-tolerant L-glutaminase produced by marine bacteria become the most desirable in food industry. The current work details the screening of L-glutaminase producing marine bacteria from Sangihe-Talaud Sea, in North of Sulawesi, Indonesia. Screening of L-glutaminase was done using a broth medium (Padma et.al., 2009) and measurement of L-glutaminase activity carried out by spectrophotometry (Imada, et.al., 1973). Identification of selected isolate was performed by analysis of 16S rRNA gene sequence. There are seven isolates showed positive results of L-glutaminase, one of them with the activity 147.99 U/L, equivalent to the specific activity of 62.32 units / mg was selected for further study.

Bacterial identification based on 16S rRNA gene sequencing has revealed the isolate 96% similarity as Pseudomonas aeruginosa strain CG-T8. Optimization of physical parameters that affect the production of L-glutaminase production showed an optimum at 30 0C, 100 rpm, pH of medium 6, and with 5% of starter inoculum. Characterization of extracellular L-glutaminase from Pseudomonas aeruginosa strain CG-T8 (II.1 isolates) showed the enzyme activity was optimum at temperature 37-45 0C, and pH 7. The enzyme activity was stable in the addition of NaCl solution up to 8% and began to decrease on addition of NaCl solution 16% and 20% with relative activity consecutively 79.00% and 74.22%. The effect of metal ions such as Mn2+, Mg2+, and Co2+ showed increased enzyme activity, whereas the addition of others metal ions (Zn2+, Fe3+, and Ca2+) decreased the activity. The molecular weights of L-glutaminase was found around 42 kDa and 145 kDa."

"[Telah dilakukan penelitian deteksi gen alkana monooksigenase (alkB) pada bakteri laut di Perairan Pulau Pari Kepulauan Seribu, Jakarta. Penelitian bertujuan untuk memperoleh isolat bakteri yang membawa gen alkB dari perairan Pulau Pari Kepulauan Seribu, Jakarta. Penelitian dilakukan selama 5 bulan sejak bulan Februari 2015 sampai bulan Mei 2015 dengan metode Polymerase Chain Reaction (PCR) pada 81 isolat yang telah diremajakan. Isolat bakteri diremajakan menggunakan medium marine agar (MA) dengan metode kuadran streak. Hasil deteksi mendapatkan satu isolat yang membawa gen alkB yaitu isolat nomor 71. Hasil amplifikasi isolat 71 menghasilkan pita DNA dengan ukuran 550 pb. Pita DNA dengan panjang 550 pb merupakan gen alkB. Hasil dari sekuensing menunjukkan bahwa Isolat 71 adalah dari spesies Bordetella sp.;Detection gene alkane monooxygenases (alkB) from marine bacteria in Pari Island Kepulauan Seribu, Jakartahas been researched. The research aims to obtain bacterial isolates that carry the gene alkBin Pari Island Kepulauan Seribu, Jakarta. The study was conducted during the five months from February 2015 to May 2015 with a method of Polymerase Chain Reaction (PCR) from 81 isolates that have been rejuvenated. Bacterial isolates rejuvenated using marine medium agar (MA) with the quadrant streak method. Obtain detection results of the isolates that carry the gene which isolates number 71. alkB amplification results of 71 isolates produce ribbon DNA with size 550 bp. DNA tape with a length of 550 bp is alkB gene.The results of sequencing showed that the isolate 71 is Bordetella sp.;Detection gene alkane monooxygenases (alkB) from marine bacteria in Pari Island Kepulauan Seribu, Jakartahas been researched. The research aims to obtain bacterial isolates that carry the gene alkBin Pari Island Kepulauan Seribu, Jakarta. The study was conducted during the five months from February 2015 to May 2015 with a method of Polymerase Chain Reaction (PCR) from 81 isolates that have been rejuvenated. Bacterial isolates rejuvenated using marine medium agar (MA) with the quadrant streak method. Obtain detection results of the isolates that carry the gene which isolates number 71. alkB amplification results of 71 isolates produce ribbon DNA with size 550 bp. DNA tape with a length of 550 bp is alkB gene.The results of sequencing showed that the isolate 71 is Bordetella sp., Detection gene alkane monooxygenases (alkB) from marine bacteria in Pari Island Kepulauan Seribu, Jakartahas been researched. The research aims to obtain bacterial isolates that carry the gene alkBin Pari Island Kepulauan Seribu, Jakarta. The study was conducted during the five months from February 2015 to May 2015 with a method of Polymerase Chain Reaction (PCR) from 81 isolates that have been rejuvenated. Bacterial isolates rejuvenated using marine medium agar (MA) with the quadrant streak method. Obtain detection results of the isolates that carry the gene which isolates number 71. alkB amplification results of 71 isolates produce ribbon DNA with size 550 bp. DNA tape with a length of 550 bp is alkB gene.The results of sequencing showed that the isolate 71 is Bordetella sp.]"

"[ABSTRAKAlkana merupakan komponen senyawa hidrokarbon terbesar sebanyak 60% penyusun utama minyak bumi. Isolat bakteri potensial pendegradasi alkana telah diisolasi dari daerah perairan tercemar tumpahan minyak di Pulau Pari. Penelitian bertujuan untuk memeroleh isolat dengan kemampuan tinggi mendegradasi alkana. Pengukuran pertumbuhan isolat bakteri dilakukan pada ƛ 600 nm dan analisis degradasi alkana dengan metode GC/MS. Hasil penelitian menunjukkan bahwa dari 15 isolat yang diuji pertumbuhannya dengan menggunakan paraffin oil terdapat 2 isolat mewakili dua tipe kurva pertumbuhan yaitu isolat 97 kelompok I dengan pertumbuhan K(+) rendah (OD < 0,1 pada hari ke-12) dan isolat 19 kelompok II dengan pertumbuhan K(+) tinggi (OD ≥ 0,5 pada hari ke-12). Analisis degradasi alkana menunjukkan penurunan luas area pada isolat 97 dengan kemampuan degradasi docosane (C22H46) paling tinggi sebesar 96,04% dan isolat 19 dengan kemampuan degradasi hexadecane (C16H34) paling tinggi sebesar 61,37%. Identifikasi molekuler menggunakan 16S rRNA menunjukkan isolat 97 sebagai Pseudoalteromonas lypolitica dan isolat 19 sebagai Vibrio alginolyticus.ABSTRACTAlkane is the largest hydrocarbon component of petroleum (60%). Potential alkane degrading bacteria have been isolated from oil contaminated waters at Pari Island. The study aims to obtain isolate with high capability of alkane degradation. The measurement of bacterial growth was performed at ƛ 600 nm and analysis of the alkane degradation with GC/MS method. Isolate 97 and 19 were selected out of 15 isolates with the highest growth represent the two groups of curve growth. Isolate 97 belong to group I with the low growth of K (+) OD <0.1 on day 12 and isolate 19 belong to group II with the high growth of K (+) ≥ 0.5 OD at day 12. The alkane degradation analysis showed isolate 97 had the highest decrease of docosane (C22H46) up to 96.04% and isolates 19 had the highest decrease of hexadecane (C16H34) up to 61.37%. The results of molecular identification using 16S rRNA indicate that isolate 97 and 19 were Pseudoalteromonas lypolitica and Vibrio alginolyticus respectively.;Alkane is the largest hydrocarbon component of petroleum (60%). Potential alkane degrading bacteria have been isolated from oil contaminated waters at Pari Island. The study aims to obtain isolate with high capability of alkane degradation. The measurement of bacterial growth was performed at ƛ 600 nm and analysis of the alkane degradation with GC/MS method. Isolate 97 and 19 were selected out of 15 isolates with the highest growth represent the two groups of curve growth. Isolate 97 belong to group I with the low growth of K (+) OD <0.1 on day 12 and isolate 19 belong to group II with the high growth of K (+) ≥ 0.5 OD at day 12. The alkane degradation analysis showed isolate 97 had the highest decrease of docosane (C22H46) up to 96.04% and isolates 19 had the highest decrease of hexadecane (C16H34) up to 61.37%. The results of molecular identification using 16S rRNA indicate that isolate 97 and 19 were Pseudoalteromonas lypolitica and Vibrio alginolyticus respectively., Alkane is the largest hydrocarbon component of petroleum (60%). Potential alkane degrading bacteria have been isolated from oil contaminated waters at Pari Island. The study aims to obtain isolate with high capability of alkane degradation. The measurement of bacterial growth was performed at ƛ 600 nm and analysis of the alkane degradation with GC/MS method. Isolate 97 and 19 were selected out of 15 isolates with the highest growth represent the two groups of curve growth. Isolate 97 belong to group I with the low growth of K (+) OD <0.1 on day 12 and isolate 19 belong to group II with the high growth of K (+) ≥ 0.5 OD at day 12. The alkane degradation analysis showed isolate 97 had the highest decrease of docosane (C22H46) up to 96.04% and isolates 19 had the highest decrease of hexadecane (C16H34) up to 61.37%. The results of molecular identification using 16S rRNA indicate that isolate 97 and 19 were Pseudoalteromonas lypolitica and Vibrio alginolyticus respectively.]"

"The diversity, ecological role and biotechnological applications of marine fungi have been addressed in numerous scientific publications in the last few years. This book addresses this need. The latest information on topics including molecular taxonomy and phylogeny, ecology of fungi in different marine habitats such as deep sea, corals, dead- sea, fungi in extreme marine environments and their biotechnological applications is reviewed. "

"[Sepanjang 1.200 km garis pantai Provinsi Kepulauan Bangka Belitung terdapat potensi ekonomi yang meliputi perikanan dan wisata bahari. Namun di sisi lain, kemiskinan justru terjadi di wilayah perdesaan yang didominasi oleh desa pesisir. Padahal disitulah letak sumberdaya kelautan dan perikanan berada. Penelitian ini bertujuan untuk mengidentifikasi sektor prioritas dari aktivitas ekonomi yang terkait dengan sektor kelautan dan memproyeksikan estimasi investasi bagi pengelolaan sektor kelautan di Provinsi Kepulauan Bangka Belitung. Analisis Input Output digunakan untuk menentukan aktivitas ekonomi yang terkait di dalamnya. Dengan pendekatan ICOR (Incremental Capital Output Ratio) diproyeksikan estimasi kebutuhan investasi selama kurun waktu 2015-2017. Hasil penelitian menunjukkan bahwa sektor prioritas dikembangkan adalah wisata bahari; perikanan budidaya; industri pengolahan dan pengawetan ikan dan hasil biota air lainnya; jasa kelautan; dan bangunan kelautan . Nilai ICOR Kelautan Provinsi Kepulauan Bangka Belitung adalah 2.93, lebih efisien dibandingkan sektor kelautan secara nasional.;Bangka Belitung Province has 1,200 km coastline with big potential economic including fisheries and marine tourism. Otherwise, poverty has occurred in rural areas with dominated by coastal villages. While therein lies the marine and fisheries resources. This study aims to identify the priority sectors of economic activity associated with the marine sector and project investment estimate for the management of the marine sector in Bangka Belitung Province. Input Output Analysis is used to determine the priority of economic activity. With the approach of ICOR (Incremental Capital Output Ratio) projected of investment for 2015-2017 period. The results showed the priority sectors to be developed are marine tourism; aquaculture; fish processing; marine services; and marine building. ICOR for Marine development of Bangka Belitung Province is 2.93. It is more efficient than the national marine sector, Bangka Belitung Province has 1,200 km coastline with big potential economic including fisheries and marine tourism. Otherwise, poverty has occurred in rural areas with dominated by coastal villages. While therein lies the marine and fisheries resources. This study aims to identify the priority sectors of economic activity associated with the marine sector and project investment estimate for the management of the marine sector in Bangka Belitung Province. Input Output Analysis is used to determine the priority of economic activity. With the approach of ICOR (Incremental Capital Output Ratio) projected of investment for 2015-2017 period. The results showed the priority sectors to be developed are marine tourism; aquaculture; fish processing; marine services; and marine building. ICOR for Marine development of Bangka Belitung Province is 2.93. It is more efficient than the national marine sector]"

"Marine-derived fungi have proven to be a rich source of cytotoxic compounds for the development of new anti cancer drugs. The aims of this research were to: 1) screen cytotoxic activity of marine fungi from Indonesian waters, 2) indentify marine fungus that produced thatproduced the most active cytotoxic compound and 3) investigate inhibition concentration 50 (IC50) value of cytotoxic compound. The fungi were isolated from marine organism collected fromWakatobi Marine National Park-South East Sulawesi, Binuangeun Beach-Banten, Manado watersNorth Sulawesi and Kepulauan Seribu Marine National Park-Jakarta. Liquid cultures of the fungiwere carried out in Malt Extract Broth and Soluble Starch Soytone medium for 4 weeks at 27?28oC without shaking. Molecular identification of fungus was conducted through PCR amplificatin usingprimers of ITS1 and ITS4 primer. Cytotoxic activity of the extract was tested by using MTT (3-(4.4-dimethylthiazol-2-yl)-2.5-diphenyl-tetrazolium bromide) method. The MTT test showed that MFW39strain exhibited the strongest cytotoxic activity. Molecular identification revealed that MFW39 marine fungus was similar to Emericella nidulans with precent identity of 99%. Mycelium and broth extract of MFW39 fungus inhibited the growth of T47D cell with IC 50 values of 21.9 and 169.3 µg/mL, respectively. Further research will be focus on to the strain of MFW39 marine fungi."

"Kanker paru-paru merupakan salah satu jenis kanker yang paling banyak diderita, terutama di negara dengan jumlah perokok dan tingkat polusi yang tinggi seperti Indonesia. Dalam beberapa tahun belakangan, perkembangan obat kanker paru jenis karsinoma bukan sel kecil diarahkan pada pengobatan multitarget karena pada pengobatan target tunggal sering kali proliferasi sel tumor dapat diaktifkan kembali melalui jalur yang lain seperti angiogenesis. Eksplorasi senyawa bioaktif dari bahan laut, termasuk fungi laut, telah mendapat perhatian khusus akhir-akhir ini sebagai pengobatan antikanker. Pada penelitian ini dilakukan pembuatan pangkalan data dan penapisan secara in silico untuk memperoleh senyawa aktif fungi laut yang berpotensi sebagai inhibitor EGFR-TK dan VEGFR2 kinase, yang masing-masing berperan sebagai agen antiproliferatif dan antiangiogenesis, menggunakan AutoDock dan Vina. Berdasarkan hasil penapisan, didapatkan tiga senyawa aktif sebagai inhibitor EGFR-TK (FU0015, FU0051, dan FU0202), satu senyawa aktif sebagai inhibitor VEGFR-2 kinase (FU0033), serta 17 senyawa potensi inhibitor multitarget (FU0018, FU0019, FU0028, FU0034, FU0037, FU0038, FU0029, FU0043, FU0079, FU0105, FU0127, FU0155, FU0156, FU0158, FU0248, FU0254, FU0261). Seluruh senyawa aktif tersebut berasal dari filum Ascomycota sehingga diharapkan dapat dilakukan eksplorasi lebih lanjut fungi laut dari filum Ascomycota.

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Lung cancer is one of the most common type of cancer, especially in countries with high numbers of smokers and high levels of pollution such as Indonesia. In the past few years, drug development of non-small cell lung cancer has been directed to a multitarget treatment as oftentimes on a single-targeted treatment proliferation of tumor cells can be reactivated via other pathways such as angiogenesis. Exploration of bioactive compounds from marine materials, including marine fungi, for anticancer treatment has become a major concern lately. In this research, database was created and in silico screening was conducted to obtain potential marine fungi active compounds as EGFR-TK and VEGFR2 kinase inhibitor, for each act as antiproliferative and antiangiogenesis agents, by using AutoDock and Vina. Based on these screening results have been identified three active compounds as the inhibitor of EGFR-TK (FU0015, FU0051, and FU0202), one active compound as the inhibitor of VEGFR-2 kinase (FU0033), and 17 compounds that potentially become a multitarget inhibitor (FU0018, FU0019, FU0028, FU0034, FU0037, FU0038, FU0029, FU0043, FU0079, FU0105, FU0127, FU0155, FU0156, FU0158, FU0248, FU0254, FU0261). All of these active compounds are from Ascomycota phylum so that further marine fungi exploration can be conducted from Ascomycota phylum."