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All Journal HAYATI Journal of Biosciences Jurnal Akuakultur Indonesia Jurnal Ilmu dan Teknologi Kelautan Tropis Torani Journal of Fisheries and Marine Science Jurnal Natur Indonesia Widyariset BERITA BIOLOGI Jurnal Akuatika Indonesia Omni-Akuatika Acta Aquatica: Aquatic Sciences Journal Jurnal Perikanan Universitas Gadjah Mada Indonesian Aquaculture Journal Jurnal Riset Akuakultur Jurnal Medik Veteriner Jurnal Penelitian Perikanan Indonesia Jurnal Iktiologi Indonesia (Indonesian Journal of Ichthyology) Techno-Fish Journal of Aquaculture and Fish Health Jurnal Lemuru : Jurnal Ilmu Perikanan dan Kelautan Indonesia Nekton Jurnal Media Akuakultur Indonesia Jurnal Penelitian Belida Indonesia Journal of Fisheries & Marine

Odang Carman

Budidaya Perairan, Institut Pertanian Bogor, Indonesia

Author-ID : 245949

Agriculture, Biological Sciences & Forestry Biochemistry, Genetics & Molecular Biology Chemical Engineering, Chemistry & Bioengineering Chemistry Decision Sciences, Operations Research & Management Earth & Planetary Sciences Economics, Econometrics & Finance Energy Engineering Environmental Science Health Professions Immunology & microbiology Industrial & Manufacturing Engineering Library & Information Science Materials Science & Nanotechnology Social Sciences Veterinary Other

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Penggunaan Gen GH sebagai Marka Molekuler DNA Gurami, Osphronemus goramy dalam Pengembangan Teknologi Surrogate Broodstock Achmad, Marlina; Alimuddin, Alimuddin; Carman, Odang; Arfah, Harton; Zairin, Muhammad
Jurnal Perikanan Universitas Gadjah Mada Vol 11, No 2 (2009)
Publisher : Universitas Gadjah Mada

The technology of fish germ cell transplantation had been established to create broodstock systems by which a target offspring can be produced from a surrogate parent. Donor cell for transplantation is derived from transgenic fish carrying green fluorescent protein gene functions as a marker to distinguish the donor from recipient cell. In this study, an alternative technique was developed for identifying gouramy-derived donor cell and Nile tilapia as recipient by PCR amplification method using growth hormone (GH) gene as a molecular marker. Specific primer for GH gouramy was designed by using Genetyx version 7 software. ß-actin gene was used as an internal control of DNA loading. The result showed that a specific PCR amplification product of 340 in length was obtained when the DNA template was from gouramy, while no PCR product from Nile tilapia. The minimum concentration of genomic DNA of gouramy mixed with a 700 ng/µl of Nile tilapia that could be detected by PCR was 1 ng/µl. Thus, PCR method with specific GH primer may be useful to detect the incorporation of donor cell in recipient gonad towards development of surrogate broodstock technology.

Aktivitas Promoter â-aktin Ikan Medaka Jepang (Oryzias latipes) pada Ikan Mas (Cyprinus carpio) ', Alimuddin; Purwanti, Lola Irma; Ath-thar, MH. Fariduddin; Muluk, Chairul; Carman, Odang; Sumantadinata, Komar
Jurnal Natur Indonesia Vol 11, No 2 (2009)
Publisher : Lembaga Penelitian dan Pengabdian kepada Masyarakat Universitas Riau

This study was conducted to examine activity of medaka (Oryzias latipes) â-actin promoter (mBP) in common carp(Cyprinus carpio) as the first step towards development of common carp transgenic in country. Gene constructpmBP-hrGFP that consists of mBA promoter and humanized Renilla reniformis green fluorescent protein gene(hrGFP) was injected into cytoplasm of one cell stage of common carp by using microinjector. PmBP-hrGFPconcentration used for microinjection was 50 μg/mL aquabides. Parameters observed were survival rate of embryo(SRe), hatching rate (HR) and expression of hrGFP gene. SRe was calculated before eggs hacthed, while hatchingrate (HR) was after all of eggs hatched. The activity of mBA promoter was analyzed by observation of hrGFP genetransient expression using a fluorescence microscope. The results of experiment showed that SRe (87,5%) andHR (79.2%) of control was respectevily higher than that of injected treatment (75.0% & 61.7%). Expression of hrGFPwas observed firstly at blastula (12 hours after fertilization) to 1-day-old larval stages (24 hours after hatching)with higher gene expression at blastula to late gastrula stages. Percentage of micronjected larvae expressinghrGFP at 6 hours after hatching reached 71.6 ± 6.7%. Conclusion was that mBA promoter could drove hrGFPexpression in common carp, hence it can be used to produce common carp transgenic by changing hrGFP withgenes correlated with important traits in aquaculture.

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.4308/hjb.18.3.135

Molecular marker is useful in the development of testicular cells transplantation for detecting donor-derived germ cells in the recipient gonad. In this study, a giant gourami (Osphronemus goramy) vasa-like gene (GgVLG) was cloned and characterized for use as a molecular marker for germ cells in this species. Nucleotide sequence analysis revealed that GgVLG comprises 2,340 bps with an open reading frame of 1,962 bps encoding 653 amino acids. The deduced amino acid sequence contained 17 arginine-glycine or arginine-glycine-glycine motifs and eight conserved motifs belonging to the DEAD-box protein family. The GgVLG sequence showed high similarity to Drosophila vasa, common carp vasa homolog and tilapia vasa homolog for 66.2, 85.9, and 90.7%, respectively. In adult tissues, the GgVLG transcripts were specifically detected in ovary and testis. In situ hybridization analysis showed that GgVLG mRNA was detected in oocytes of the ovary and spermatogonia of the testis. There was no signal detected in the spermatocytes, spermatids and other gonadal somatic cells. Thus, consensus sequences, specific localization of GgVLG mRNA in the germ cells, amino acid sequence similarity and phylogenic analysis all suggest that GgVLG is the giant gourami vasa-like gene. Further, GgVLG can be used as a molecular marker for giant gourami germ cells.

Heat Shock and Its Consequences on Early Life Performance of Stripped Catfis (Pangasianodon hypophthalmus) Prama Hartami; Odang Carman; Muhammad Zairin; Alimuddin Alimuddin
Journal Omni-Akuatika Omni-Akuatika Special Issue 2nd Kripik SCiFiMaS
Publisher : Fisheries and Marine Science Faculty - Jenderal Soedirman University

Researchers have widely applied heat shock on zygote stadia of domesticated aquatic animals especially for the purpose of ploidy manipulation in fish to accelerate growth, intermediate products for the production of infertile seeds, providing prospective brood stock as well as the monosex population. This is certainly an interesting study to see how far the impact of heat shock on the early development stages. This experiment used a 42 0C heat shock for 2.5 minutes on the zygote at different initial time i.e. 28.5; 29; 29.5; 30 and 30.5 minutes after fertilization. All treated larvae and control were reared in a 25 liters plastic container at density of 5 larvae per liter. The results showed that high percentage of fertilization rate were 92.61 % to 96.32 % and hatching rate was 85.33 % without any abnormalities were achieved in the control. While in all treatments had a very low hatching rate of 4.12 % to 8.93 % with relatively high abnormalities of 12.36 % to 27.60 % and a significant differences (P<0.05) compared to controls, but survival rate, specific growth rate and feed conversion ratio after 30 days rearing period showed no significant difference (P>0,05). In terms of seed production, the heat shock treatment will limit 78 % to 82 % of larvae production.

GROWTH IN NURSERY AND GROW-OUT PHASES OF WHITE SHRIMP AFTER IMMERSED IN RECOMBINANT GIANT GROUPER GROWTH HORMONE Aulia Saputra; Odang Carman; . Alimuddin
Jurnal Ilmu dan Teknologi Kelautan Tropis Vol. 7 No. 2 (2015): Elektronik Jurnal Ilmu dan Teknologi Kelautan Tropis
Publisher : Department of Marine Science and Technology, Faculty of Fisheries and Marine Science, IPB University

The growth of white shrimp (Litopenaeus vannamei) can be improved by using recombinant fish growth hormone through immersion. This research was performed to evaluate the white shrimp growth at nursery and grow-out phases after recombinant giant grouper growth hormone (rElGH) immersion. Shrimp were immersed at different stages in one liter seawater containing 15 mg rElGH for two hours. At the nursery stage 30,000 PL4 that previously immersed at nauplius stage (treatment A1), at PL4 (treatment B1) and control without rElGH immersion (K1) were reared in fiber tanks containing 750 L seawater for 8 days. At the grow-out phase, 100 PL11 that have been immersed in rElGH solution at nauplius stage (treatment A2), at PL4 (B2), PL11 (C2) and control without rElGH immersion (K2) were separately reared in fiber tanks containing 750 L seawater for 55 days. Each treatment consisted of three replications. The results showed that at the end of the nursery phase, B1 treatment increased 19% of body length, 30.2% of the body weight and decreased the coefficient of length variation 34.9% compared to control K1 (P<0.05). At the grow-out phase, C2 treatment enhanced 38.2% of body weight and 32% of biomass compared with control K2 (P<0.05). Thus, hatchery is better to immerse PL4, and the farmer should used rElGH-immersed PL11 for growing-out.Keywords: growth promoting, nursery, grow out, Litopenaeus vannamei, rElGH

TRANSPLANTATION OF GIANT GOURAMY (Osphronemus gouramy) TESTICULAR CELLS IN EARLY HATCHING TILAPIA (Oreochromis niloticus) LARVAE Jasmadi Jasmadi; Odang Carman; Alimuddin Alimuddin
Widyariset Vol 2, No 2 (2016): Widyariset
Publisher : Pusbindiklat - LIPI

Cell transplantation technology has been widely developed in mammals, but less implemented in inland aquaculture fish. Giant gouramy (Osphronemus gouramy) is one of important comercial aquaculture commodities that has a relatively long first reproductive cycle compared to the tilapia (Oreochromis niloticus). Tilapia has a faster reproductive cycle and potential as giant gouramy surrogate broodstock. This study was aimed to applicate testicular cell transplantation technology of giant gouramy in tilapia larvae and to evaluate its success rate trough donor cell colonization. Tilapia larvae of 1-2 dph (days post hatching) and 3-4 dph were injected with ±20.000 giant gouramy testicular cells in the peritoneal cavity, and then groomed for two months. Cell colonization of spermatogonium donor was determined by Polymerase Chain Reaction (PCR), using giant gouramy F1-Growth Hormone and R1-Growth Hormone primers. The result of cell dissociation showed that a bigger giant gouramy (827 g) had lower of spermatogonia composition (4.45%) than a smaller gouramy (608 g) (14.96%). Donor cell colonization in 1-2 dph recipient was higher (100%) than in 3-4 dph recipient (75%). Whereas recipient Survival Rate (SR) was 89.34% for 1-2 dph recipient and 98.96% for 3-4 dph recipient respectively. This study suggests that testicular cell transplantation technology of giant gouramy could be appllied to tilapia (Xenotransplantation) and cell transplantation has a better performance in 1-2 dph than in 3-4 dph recipients. With such success, there is a high potential that the giant gouramy cultivation can be increased through the cell transplantation technology.

RAGAM FENOTIPE IKAN TENGADAK Barbonymus schwanenfeldii (Bleeker 1854) HASIL SILANG LUAR Firda Amalia Sukma; Muhammad Fariduddin Ath-Thar; Odang Carman; Deni Radona
BERITA BIOLOGI Vol 19, No 1 (2020)
Publisher : Research Center for Biology-Indonesian Institute of Sciences

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14203/beritabiologi.v19i1.3773

Outbreed may increase genetic diversity and produce better offspring. Meanwhile, genetic diversity can be inferred from phenotypes variability. This study aimed to analyze the diversity of phenotypic characters from four populations of tinfoil barb outbreed, namely Java (J), Kalimantan (K), ♀ Java × ♂ Kalimantan (JK) and ♀ Kalimantan × ♂ Java (KJ).Analysis of the phenotypic diversity was calculated based on truss morphometric on 30 individuals sampled from each populations. The growth and survival rate were measured for 40 days reared. The study was conducted experimentally using a completely randomized design (CDR) with three replications.Rearing four population of tinfoil barb, beginning with acclimatization for two weeks and was continued reared using 12 aquaria40x30x30 cm3. Each aquaria was filled with 10 individual seeds/20 L-1 water with the size of 18,66±1,34 g weight and 8,28±0,34 cm of length. Feeding was done three times a day on ad-libitum using commercial pellet with protein content of31˗33%. The result of the canonical function analysis of truss morfometrik thetinfoil barb on 21 characteris indicated that the individual morphological characterof population of the tinfoil barb outbreed (JK and KJ) interrelated with each other.The highest sharing component value of inter population was obtained on the fish from outbreed of KJ and JK (13,3%), while the highest of intra population was obtained of K (96,7%) and the lowest of JK (86,7%). The highest survival rate (100%) was recorded on the JK population and significantly different (P>0,05) with survival rate of 90% observed in the J population.

Embriogenesis, Perkembangan Larva dan Viabilitas Reproduksi Ikan Pelangi Iriatherina Werneri Meinken, 1974 pada Kondisi Laboratorium Muh. Herjayanto; Odang Carman; Dinar Tri Soelistyowati
Akuatika Indonesia Vol 2, No 1 (2017): Jurnal Akuatika Indonesia (JAkI)
Publisher : Direktorat Sumber Daya Akademik dan Perpustakaan Universitas Padjadjaran, Grha. Kandaga (P

Ikan pelangi Iriatherina werneri diperdagangkan sebagai ikan hias, karena memiliki warna dan bentuk sirip yang indah terutama untuk individu jantan. Perkembangan budidaya ikan pelangi terkendala oleh kurangnya informasi biologi terkait perkembangan embrio (embriogenesis), perkembangan larva, viabilitas reproduksi dan sejarah kehidupannya. Tujuan dari penelitian untuk mengkaji embriogenesis, perkembangan larva dan viabilitas reproduksi pada ikan pelangi I. werneri sebagai informasi dasar untuk menunjang kegiatan budidaya dan konservasi. Pengamatan embriogenesis menggunakan 100 butir embrio yang dimasukkan pada empat buah wadah inkubasi berukuran (19,5 × 13,5 × 8,5) cm3. Pengamatan viabilitas reproduksi dan pertumbuhan menggunakan 200 butir embrio yang dimasukkan pada lima buah wadah berukuran (19,5 × 19,5 × 19,5) cm3. Hasil penelitian menunjukkan bahwa embrio ikan pelangi berkembang mulai dari fase pembelahan sel, morula, blastula, gastrula, organogenesis dan menetas menjadi larva pada saat 124 jam 5 menit setelah pembuahan. Telur mulai menetas pada hari keempat (15,11%) dan berakhir pada hari keenam (23,35%) dengan puncak penetasan terjadi pada hari kelima (61,54%) setelah pembuahan. Ikan telah menjadi juvenil pada umur 35 hari setelah menetas dengan panjang total >12 mm. Viabilitas reproduksi I. werneri pada penelitian ini yaitu tingkat penetasan sebesar 62,04%; tingkat kelangsungan hidup sampai umur 50 hari setelah menetas sebesar 62,72% dan ikan jantan secara alami sebanyak 20%.

Maskulinisasi Ikan Pelangi Iriatherina werneri Meinken, 1974 Menggunakan Hormon 17α-Metiltestosteron Melalui Perendaman Embrio Muh. Herjayanto; Odang Carman; Dinar Tri Soelistyowati
Akuatika Indonesia Vol 4, No 2 (2019): Jurnal Akuatika Indonesia (JAkI)
Publisher : Direktorat Sumber Daya Akademik dan Perpustakaan Universitas Padjadjaran, Grha. Kandaga (P

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.24198/jaki.v%vi%i.21516

Individu jantan ikan pelangi Iriatherina werneri lebih digemari sebagai ikan hias dibandingkan individu betina. Ikan jantan memiliki bentuk sirip punggung kedua dan sirip anal yang panjang seperti filament dan warna tubuh yang indah. Namun permasalahannya adalah secara alami populasi ikan jantan yang dihasilkan rendah. Oleh karena itu, maskulinisasi diperlukan untuk meningkatkan jumlah populasi ikan jantan. Teknik maskulinisasi menggunakan perendaman embrio fase bintik mata di dalam larutan hormon 17α-metiltestosteron (MT). Tujuan penelitian yaitu mengkaji persentase ikan jantan, tingkat penetasan telur, sintasan, abnormalitas dan pertumbuhan panjang total ikan pelangi melalui perendaman embrio pada dosis MT dan lama perendaman berbeda. Embrio yang digunakan pada fase organogenesis berumur 64 jam 40 menit setelah pembuahan. Perlakuan yang digunakan yaitu dosis MT 15, 30 dan 45 mg L-1, serta lama perendaman selama 6, 12 dan 24 jam. Hasil penelitian menunjukkan kombinasi perlakuan MT dosis 30 mg L-1 dan lama perendaman 6 jam merupakan kombinasi perlakuan terbaik yaitu menghasilkan ikan jantan 56,67%. Kombinasi perlakuan tersebut juga menghasilkan tingkat penetasan telur, abnormalitas dan pertumbuhan panjang total ikan pelangi pada kisaran normal. Pemberian MT dosis tinggi dan pemaparannya yang lama pada embrio dapat menurunkan performa penetasan telur dan kualitas larva ikan pelangi. Bentuk abnormal terlihat pada tulang belakang bengkok dan bentuk mulut yang tidak sempurna. Kajian maskulinisasi pada ikan pelangi masih perlu dilakukan untuk memperoleh sintasan yang lebih baik.

Genotype diversity and morphometric of tinfoil barb Barbonymus schwanenfeldii (Bleeker 1854) from Sumatera, Java, and Kalimantan Deni Radona; Dinar Tri Soelistyowati; Odang Carman; Rudhy Gustiano
Jurnal Iktiologi Indonesia Vol 16 No 3 (2016): October 2016
Publisher : Masyarakat Iktiologi Indonesia (Indonesian Ichthyological Society)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.32491/jii.v16i3.25

Study on genotype and phenotype diversity of initial population tinfoil barb from Sumatera, Java and Kalimantan is an effort to use genetic sources of tinfoil barb for sustainable aquaculture. This study was to evaluate the diversity of genotype and phenotype of tinfoil barb from Sumatra, Java and Kalimantan. Analysis of genotype diversity was con- ducted by RAPD methods using primer (OPA 08, OPA 09 and OPC 02) and phenotype based on truss morphometric measurement. The result showed that the highest genetic polymorphism (40%) was found in the male population of Java and female from Kalimantan with heterozygosity 0.18; while the lowest polymorphism was detected in the female population from Java (18%) with the heterozigosity level at 0.08. Based on the relationship between tinfoil barb from Java, Sumatera and Kalimantan by using three primer of RAPD showed that the genetic distance ranged from 0.48- 0.55, whereas between male and female population was ranged from 0.19-0.24. Canonical analysis using truss morpho- metric from 21 measured characters among three populations showed the different kind of genetic dispersion. From intrapopulation genetic sharing percentage, the highest interpopulation genetic sharing component was found in the tinfoil barb from Java (66.7-86.7 %), while interpopulation genetic sharing component ranged 0-6 % and 0 % were found in the tinfoil barb from Kalimantan and Sumatera, respectively. According to our results, the genotype diversity and phenotype of tinfoil male from Java and female from Kalimantan are genetic resources for developing tinfoil barb aquaculture. Abstrak Studi keragaman genotipe dan fenotipe populasi awal ikan tengadak (Barbonymus schwanenfeldii) asal Sumatera, Jawa, dan Kalimantan merupakan upaya pemanfaatan sumber daya genetik ikan tengadak untuk kegiatan budi daya secara berkelanjutan. Tujuan penelitian ini adalah melakukan evaluasi keragaman genotipe dan fenotipe ikan tengadak asal Sumatera, Jawa, dan Kalimantan. Analisis keragaman genotipe dilakukan secara molekuler dengan metode Random Amplified Polymorphism DNA (RAPD) menggunakan primer OPA 08, OPA 09 dan OPC 02 sedangkan keragaman fenotipe dilakukan berdasarkan pengukuran truss morphometric. Hasil penelitian menunjukkan polimorfisme genetik tertinggi (40%) ditemukan pada ikan jantan populasi asal Jawa dan ikan betina asal Kalimantan dengan nilai heterozi- gositas tertinggi 0,18 sedangkan polimorfisme terendah (18%) ditemukan pada ikan betina populasi asal Jawa dengan tingkat heterozigositas 0,08. Jarak genetik ketiga populasi berkisar 0,48-0,55 sedangkan antara ikan jantan dan betina berki-sar 0,19-0,24. Hasil analisis fungsi kanonikal truss morfometrik ikan tengadak pada 21 karakter terukur menun- jukkan sebaran pengukuran ketiga populasi berada pada kuadran yang berbeda. Persentase indeks keseragaman intra- populasi menunjukkan indeks keseragaman genetik tertinggi pada populasi Jawa (66,7-86,7 %) dengan indeks kesera- gaman interpopulasi (0-6%) pada populasi Kalimantan dan (0%) pada populasi Sumatera. Berdasarkan data keragaman genotipe dan fenotipe ikan jantan asal Jawa dan ikan betina asal Kalimantan berpotensi sebagai sumber genetik donor untuk pengembangan budidaya ikan tengadak.

Co-Authors ', Alimuddin , Alimuddin , Rahman, , . Syafiuddin Abinawanto Abinawanto Agus Oman Sudrajat Ahmad Teduh Alimuddin Alimuddin Alimuddin Alimuddin Alimuddin Alimuddin Alimuddin Alimuddin Alimuddin Alimuddin Alimuddin Alimuddin Alimuddin Alimuddin Alimuddin Alimuddin Alimuddin Alimuddin Alimuddin Alimuddin Alimuddin Alimuddin Alimuddin Alimuddin Alimuddin Amalia Hayati Anang Hari Kristanto Andi Aliah Hidayani Andri Iskandar Angraini, Siti Rena Yulia ANNA OCTAVERA Astri Ayuningtias Aulia Saputra Aulia Saputra Avarre, Jean-Christophe Ayi Santika Budyansah Siregar Cahyono, Tatak Dwi Cecilia Eny Indriastuti Chairul Muluk Ching-Fong Chang D.S. Sjafei Dede Hermawan DEDI JUSADI Dendi Hidayatullah, Dendi Deni Radona Deni Radona Deni Radona Deni Radona, Deni Dian Eka Ramadhani Dian R Herdianto Didik Ariyanto Didik Ariyanto Dinar Tri Soelistyowati Dita Puji Laksana Djamhuriyah S. Said Eddy Supriyono Eka Haris Nurfauzi Elfrida Ratnawati Enang Harris Eni Kusrini Estu Nugroho Eva Ayuzar Fajar Maulana . Fauzan Wahib Alsani Firda Amalia Sukma Firmansyah, Rodhi Flandrianto S. Palimirmo Giri Maruto Darmawangsa GORO YOSHIZAKI Goro Yoshizaki Goro Yoshizaki Guan-Chung Wu Handika Gilang Pramana Putra Harton Arfah Hasan Nasrullah Hendriana, Andri Herjayanto, Muh. Hidayat Hidayat Hidayatush Sholihin Hylda Khairah Putri, Hylda Khairah I. Andriani I. Herviani Ibrahim Satrio Faqih Ibrahim, Yusran Iis Diatin Indra Lesmana Irin Iriana Kusmini IRMA ANDRIYANI Irvan Faizal Irvan Faizal Irvan Faizal Irwan Irwan Iskandar, Andri Jasmadi Jasmadi K. Sumantadinata Kadarusman . Kaliky, Nunun Ainun Putri Sari Banun Kesit Tisna Wibowo Komar Sumantadinata Komar Sumantadinata Komar Sumantadinata Komar Sumantadinata Komar Sumantadinata Komar Sumantadinata Komar Sumantadinata Komar Sumantadinata Komar Sumantadinata Kukuh Adiyana, Kukuh Laurent Pouyaud Lies Emmawati Hadie Lies Emmawati Hadie Lilis Nurjannah Lina Mulyani Lisa Ruliaty Lola Irma Purwanti M. Syaifudin M. Syukur M. Zairin Junior Maharani, Adinda Marlina Achmad Maskur Maskur MH. Fariduddin Ath-thar Mia Setiawati Moh. Abduh Nurhidayat Mubinun Mubinun Muh. Herjayanto Muhamad Fathurrizki Darmawan Muhamad Syukur Muhammad Agus Muljanto MUHAMMAD AGUS SUPRAYUDI Muhammad Fakhri Muhammad Muhammad Muhammad Rafi Muhammad Sami Daryanto Muhammad Zairin Muhammad Zairin Muhammad Zairin Jr Muhammad Zairin Jr. Muslim Muslim N. Sugiri Nadia Mega Aryani, Nadia Mega NM Fatih Asror AM Novi Megawati Nugraha, Media Fitri Isma Nur Bambang Priyo Utomo Prama Hartami Prama Hartami Raden Roro Sri Pudji Sinarni Dewi Rahma Vida Anandasari, Rahma Vida Rahman Rahman Rahmat Hidayat Rahmat Hidayat Rahmi, Kurnia Anggraini Ratu Siti Aliah Rezki, Dinda Wahyu RIDWAN AFFANDI Ronny Rachman Noor Rudhy Gustiano Rudhy Gustiano S. Purwati Salamah Salamah Salsabilla Galby Fataya Samalei, Ermianus Siti Subaidah Siti Subaidah Sri Nuryati Sri Setyo Wulandari, Sri Setyo Sri Sundari Subandriyo Subandriyo Sukenda . Sukenda Sukenda Sumie Etoh Syahril, Alfis Tatang Juanda Toshio Takeuchi Tristiana Yuniarti Wartono Hadie Wartono Hadie Wasmen Manalu Wedaraningtyas Nugrahani Wicaksono, Aryo Wenang Yogi Himawan Yumaidawati, Nurfitriani Siti Yuni Puji Hastuti Zairin Jr., Muhammad

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