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All Journal HAYATI Journal of Biosciences Jurnal Agronomi Indonesia (Indonesian Journal of Agronomy) Jurnal Ilmu Pertanian Indonesia Jurnal Fitopatologi Indonesia Jurnal Teknologi Industri Pertanian Jurnal Pengolahan Hasil Perikanan Indonesia Jurnal Akuatika Microbiology Indonesia Biota: Jurnal Ilmiah Ilmu-Ilmu Hayati Agrointek Jurnal Hortikultura Current Biochemistry BIOTIK: Jurnal Ilmiah Biologi Teknologi dan Kependidikan Jurnal Pengelolaan Sumberdaya Alam dan Lingkungan (Journal of Natural Resources and Environmental Management) Indonesian Journal of Biotechnology Agrokreatif Jurnal Ilmiah Pengabdian kepada Masyarakat Jurnal Sumberdaya Hayati Journal of Tropical Biodiversity and Biotechnology Jurnal Bioteknologi & Biosains Indonesia (JBBI) Jurnal Biodjati Squalen Bulletin of Marine and Fisheries Postharvest and Biotechnology Majalah Ilmiah Biologi BIOSFERA: A Scientific Journal Biosaintifika: Journal of Biology & Biology Education Jurnal Purifikasi Jurnal Pascapanen dan Bioteknologi Kelautan dan Perikanan Menara Perkebunan Jurnal Mangifera Edu Journal of Microbial Systematics and Biotechnology Konservasi Hayati Prosiding Seminar Nasional Biologi, Teknologi dan Kependidikan (Biotik) MADURANCH: JURNAL ILMU PETERNAKAN Makara Journal of Science International Journal of Oil Palm

NISA RACHMANIA MUBARIK

Bogor Agricultural University

Author-ID : 322460

Agriculture, Biological Sciences & Forestry Biochemistry, Genetics & Molecular Biology Chemical Engineering, Chemistry & Bioengineering Decision Sciences, Operations Research & Management Dentistry Earth & Planetary Sciences Economics, Econometrics & Finance Education Energy Engineering Environmental Science Immunology & microbiology Industrial & Manufacturing Engineering Languange, Linguistic, Communication & Media Library & Information Science Materials Science & Nanotechnology Medicine & Pharmacology Neuroscience Nursing Public Health Social Sciences Other

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APLIKASI PUPUK HAYATI (PLANT GROWTH PROMOTING RHIZOBACTERIA) YANG TELAH DISIMPAN TERHADAP PERTUMBUHAN TANAMAN JAGUNG Var. BISMA Nurul Hidayati; Hamim Hamim; Nisa Rachmania Mubarik
MaduRanch: Jurnal Ilmu-Ilmu Peternakan Vol 2, No 1 (2017): MaduRanch: Jurnal Ilmu-Ilmu Peternakan
Publisher : MaduRanch: Jurnal Ilmu-Ilmu Peternakan

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (128.309 KB)

Aplikasi pupuk hayati yang mengandung mikrob hidup dapat memacu pertumbuhan tanaman. Percobaan dimaksudkan untuk menguji viabilitas Bacillus sp., Pseudomonas sp., Azospirillum sp., dan Azotobacter sp. yang terdapat pada pupuk hayati dikeringkan dengan metode kering beku pada beberapa bulan penyimpanan. Viabilitas sel bakteri diuji setelah disimpan 0, 1, 2, 4, dan 6 bulan. Pupuk hayati tersebut diaplikasi pada tanaman jagung var. Bisma untuk diamati efektivitasnya. Penelitian ini dilakukan di rumah kaca dengan menggunakan metode Rancangan Acak Lengkap (RAL) yang terdiri atas 8 perlakuan dengan 5 ulangan. Perlakuan tanah tanpa pemupukan (P1); tanah dengan pupuk NPK (P2); tanah dengan kompos (P3); tanah dengan kompos dan pupuk hayati penyimpanan 0, 1, 2, 4, dan 6 bulan (P4-P8). Hasil uji menunjukkan viabilitas bakteri sedikit menurun setelah proses kering beku (freeze drying) kemudian stabil sampai penyimpanan 2 bulan. Setelah 2 bulan, viabilitas masing-masing bakteri yang terkandung dalam pupuk hayati menurun. Aplikasi pupuk hayati penyimpanan 0, 1, 2, 4, dan 6 bulan meningkatkan pertumbuhan dan produksi tanaman jagung. Namun semakin lama penyimpanan menyebabkan efektivitas pupuk hayati untuk mendukung pertumbuhan dan produksi jagung menurun. Produksi jagung menurun dari 109.36 gram pada P5menjadi 70.46 gram pada P8.

Karakterisasi Enzim Selulase PMP 0126Y dari Limbah Pengolahan Agar Ekowati Chasanah; Isna Rahma Dini; Nisa Rachmania Mubarik
Jurnal Pascapanen dan Bioteknologi Kelautan dan Perikanan Vol 8, No 2 (2013): Desember 2013
Publisher : Balai Besar Riset Pengolahan Produk dan Bioteknologi Kelautan dan Perikanan

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.15578/jpbkp.v8i2.41

Hasil penapisan bakteri penghasil enzim selulase terdahulu mendapatkan isolat PMP 0126 sebagai isolat yang berpotensi yang diisolasi dari limbah pengolahan agar skala UKM di Pamengpeuk, Garut. Isolat tersebut ternyata belum merupakan koloni tunggal, terdiri dari 2 isolat bakteri yaitu PMP 0126Y dan PMP 0126W. Isolat PMP 0126Y memiliki kemampuan mendegradasi selulosa yang lebih besar dibanding PMP 0126W. Tujuan dari penelitian ini adalah untuk memproduksi dan mengkarakterisasi enzim selulase dari isolat PMP 0126Y, serta mengidentifikasi isolat tersebut. Hasil penelitian menunjukkan bahwa enzim selulase diproduksi optimum pada hari ke-3 kultivasi menggunakan medium cair berisi CMC 1%. Enzim kasar yang diperoleh dapat bekerja optimal pada suhu 30 °C dan pH 5, dapat ditingkatkan aktivitasnya dengan ion logam dalam bentuk garam CaCl2 dan ZnCl2 5 mM.. Pemurnian dengan sistem penukar anion dapat meningkatkan aktivitas enzim 15x dengan perolehan 20%. Dari hasil SDS-PAGE terlihat bahwa ada 3 selulase dengan perkiraan berat molekul 39, 30, dan 14 kDa. Enzim kasar ini memiliki kemampuan menghidrolisis limbah pengolahan agar sebaik ketika memecah substrat CMC, yang mengindikasikan bahwa enzim dari isolat ini berpotensi sebagai kandidat agen sakarifikasi pada produksi bioetanol. Identifikasi bakteri dengan 16S-rDNA menunjukkan bahwa isolat ini memiliki kemiripan 96% dengan bakteri Chryseobacterium indologenes McR-1.

Optimum Age of Starter for Microbial Transglutaminase (MTGase) Production Produced by Streptomyces thioluteus TTA 02 SDS 14 and Characterization of Crude Enzyme Dewi Seswita Zilda; Yusro Nuri Fawzya; Lia Siti Nur'amaliyah; Hana Nurullita Prestisia; Nisa Rachmania Mubarik; Puspita Lisdiyanti
Squalen, Buletin Pascapanen dan Bioteknologi Kelautan dan Perikanan Vol 12, No 1 (2017): May 2017
Publisher : Research and Development Center for Marine and Fisheries Product Processing and Biotechnol

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.15578/squalen.v12i1.283

The condition of starter plays important role in enzyme production. Optimum starter will lead to the optimum yield of enzyme production. The experiments which were aimed to obtain the optimum age for starter of Streptomyces thioluteus TTA 02 SDS 14 from solid as well as liquid medium had been carried out which would be used for transglutaminase production. Medium used for culture maintenance, starter optimization and enzyme production was described by Bahrim. The result showed that S. thioluteus TTA 02 SDS 14 was ready to be used as starter after being cultured on solid medium continued in liquid medium each for 6 days. The enzyme production in a bioreactor using optimized starter produced enzyme with the highest activity after being fermented for 2 days with 150 rpm agitation. The crude enzyme active optimally at 45-50 oC, pH of 6 and no effect of metal ion and inhibitor on enzyme activity.

Purification and Characterization of Transglutaminase from Local Streptomyces Sp. TTA 02 SDS 14 Lia Siti Nur'amaliyah; Dewi Seswita Zilda; Nisa Rachmania Mubarik
Squalen, Buletin Pascapanen dan Bioteknologi Kelautan dan Perikanan Vol 11, No 3 (2016): December 2016
Publisher : Research and Development Center for Marine and Fisheries Product Processing and Biotechnol

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.15578/squalen.v11i3.234

Streptomyces sp. TTA 02 SDS 14 is a transglutaminase producing bacteria which previously had been screened along with more than one hundred isolates. This research aimed to purify and characterize transglutaminase from this strain. Transglutaminase was purified from crude enzyme by ultrafiltration, Q-Sepharose ion exchange chromatography and Sepacryl S200 size exclusion chromatography sequentially, obtaining yield and purification fold of 1.36% and 27 folds, respectively. The molecular weight of the purified transglutaminase was 72 kDa detected by zymogram gel electrophoresis. The optimum temperature and pH were 50°C and 6. The transglutaminase was stable at 45°C and could be activated in the presence of 5 mM and 10 mM of Na+, K+, Li+,Ca2+, Mg2+, BPB (4-bromo-phenacyl bromide), and IAA (iodo acetamide acid), but the activity was inhibited by the presence of Cu+, Zn2+, and PMSF (phenyl methyl sulfonyl fluoride).

Konstruksi Mutan Pseudomonas sp. untuk Meningkatkan Produksi Indole Acetic Acid (IAA) melalui Mutagenesis dengan Transposon Aris Tri Wahyudi; Mutiha Panjaitan; Nisa Rachmania
Majalah Ilmiah Biologi BIOSFERA: A Scientific Journal Vol 26, No 3 (2009)
Publisher : Fakultas Biologi | Universitas Jenderal Soedirman

Pseudomonas sp. is one of bacterial groups having ability to promote plant growth and health. Of a hundred successfully isolated Pseudomonas sp. from soybean rhyzosphere, 98 were found to produce indole acetic acid (IAA) ranging from 0.33 to 16.02 ppm. These isolates are bacilli, motile, Gram negative, and showing positive oxidase assay. One of them, i.e. Pseudomonas sp. CRB17, can promote plant growth by means of significant stimulation of primary root length and lateral root number. This isolate was then subject to mutagenesis using transposon Mini-Tn5Km1 to increase IAA production. Mutagenesis was done by conjugation between E coli S17-1 (l pir) carrying transposon mini-Tn5Km1 (donor) and Pseudomonas sp. (recipient), resulting in conjugation frequency of approximately 3.1 x 10-5 cell per recipient. The resulted CRB17 mutants were then tested for their ability to produce IAA, one of which showed an increment of IAA production up to 77.5%, while some others showed no significant change or even had a reduction to 55.3%. Sequence analyisis of 16S rRNA gene of Pseudomonas sp. CRB17 indicated that it has a high homology with that of Pseudomonas plecoglossicida (identical value of 99%). The results recommends that mutagenesis using transposon can be applied to increase IAA production, especially in Pseudomonas sp. CRB17.

REHABILITASI LAHAN BEKAS TAMBANG DI QUARRY PT INDOCEMENT HAMBALANG DENGAN MENGGUNAKAN TANAMAN LEGUM DAN PUPUK HAYATI Marini Adani; Hirmas Fuady Putra; Ahmad Suryadi; Idin Abidin; Nisa Rachmania Mubarik
Prosiding Seminar Nasional Biotik Vol 9, No 1 (2021): PROSIDING SEMINAR NASIONAL BIOTIK IX 2021
Publisher : Prosiding Seminar Nasional Biotik

Rehabilitasi pada tanah bekas tambang di kawasan reklamasi biasanya menggunakan top soil yang berasal dari area yang subur dan selanjutnya dilakukan revegetasi. Penambangan sandy clay di kawasan PT Indocement merupakan area terbuka yang akan dilakukan reklamasi. Proses revegetasi di kawasan ini akan menggunakan kompos yang dicampur dengan bakteri tanah yang berasal dari area reklamasi PT Indocement di Palimanan Cirebon. Penelitian ini bertujuan untuk (1) memanfaatkan formulasi yang mengandung bakteri pelarut P dan K, bakteri penambat N, penghasil IAA sebagai pupuk hayati pada tanaman yang ditanam di lahan bekas tambang di Hambalang, (2) melakukan revegetasi di area bekas tambang dengan menggunakan tanaman legum, seperti lamtoro (Leucaena leucocephala), ki hujan (Albizia saman), and angsana (Pterocarpus indicus) yang diaplikasikan dengan menggunakan dan kompos dan konsorsium bakteri dengan metode penggaruan (ripping) dan tanpa penggaruan pada tanah, dan (3) melakukan evaluasi kondisi ekologi pada kawasa bekas tambang. Hasil yang diperoleh menunjukkan perlakuan penanaman dengan cara ripping dan pemberian kompos serta bakteri memberikan hasil yang lebih tinggi daripada kontrol tanpa ripping untuk tanaman yang sengaja ditanam (assisted). Perlakuan dengan ripping disertai pemberian kompos, dan bakteri menunjukkan tanaman tumbuh lebih tinggi daripada perlakuan hanya dengan ripping dan tanpa ripping pada jenis tanaman lamtoro dan angsana.

EFEKTIVITAS PENGHAMBATAN BAKTERI KITINOLITIK TERHADAP Fusarium proliferatum Siti Azzira Rahma; Nisa Rachmania Mubarik; Lisdar A Manaf
Prosiding Seminar Nasional Biotik Vol 9, No 2 (2021): PROSIDING SEMINAR NASIONAL BIOTIK IX 2021
Publisher : Prosiding Seminar Nasional Biotik

Fusarium spp. merupakan penyebab penyakit pada beberapa jenis tanaman salah satunya bawang merah sehingga dapat menurunkan produktivitas tanaman bawang merah (Allium cepa L.). Bakteri kitinolitik diketahui memiliki sifat antagonis terhadap Fusarium spp. Penelitian bertujuan mengetahui kemampuan isolat bakteri ABP5.1, ABP5.2.2, ABS4.1.2, BBP5.2.2 yang berasal dari pertanian bawang merah dalam menghambat pertumbuhan F. proliferatum. Sebanyak empat isolat bakteri terpilih hasil isolasi dari penelitian sebelumnya diuji kemampuannya dalam menghambat pertumbuhan Fusarium proliferatum. Tahapan penelitian terdiri atas karakterisasi isolat, uji aktivitas kitinolitik, uji antagonis antar isolat bakteri, dan uji antagonis isolat bakteri terhadap cendawan Fusarium proliferatum. Keempat isolat bakteri ABP5.1, ABP5.2.2, ABS4.1.2, dan BBP5.2.1 merupakan bakteri gram negatif. Uji kualitatif kitinolitik menunjukkan keempat isolat menghasilkan zona bening dengan indeks kitinolitik antara 0,04-1,0. Isolat bakteri ABS4.1.2 memiliki nilai indeks kitinolitik terbesar yaitu 1,09. Uji antagonis antar isolat bakteri menunjukkan hasil keempat isolat bakteri tidak bersifat saling antagonis. Uji antagonis bakteri terhadap cendawan Fusarium proliferatum dengan metode dual culture menunjukkan bahwa sebanyak dua dari empat isolat mampu menghambat pertumbuhan cendawan F.proliferatum. Isolat ABP5.2.2 memiliki daya hambat terbesar yaitu 41%, sedangkan isolat ABS4.1.2 memiliki daya hambat sebesar 40%.

Characterization and application of nitrogen-fixing and indole-3-acetic acid producing bacteria A13 in Oil Palm (Elaeisguineensis Jacq.) seedling Ismi Isti'anah; Nisa Rachmania Mubarik; Aris Tjahjoleksono
Journal of Microbial Systematics and Biotechnology Vol 3, No 1 (2021): August 2021
Publisher : Microbiology Division, Research Center for Biology, Indonesian Institute of Sciences

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.37604/jmsb.v3i1.77

Oil palm plantations have a good prospect in Indonesia. One of the efforts to improve the productivity of oil palm plantation is the application of bacteria as biological fertilizer. The research was conducted to characterize and apply the nitrogen-fixing and indole-3-acetic acid producing bacteria in oil palm seedlings. The bacteria was isolated from soil samples which taken from Taman Nasional Bukit Dua Belas (TNBD) Jambi. Nitrogen free bromthymol blue (NFB) is used as media for nitrogen-fixing bacterial isolation. Selected isolate named A13 had an ability to form white pellicle on the surface of the semisolid medium, increased the pH, and changed the color of medium from green to blue Isolate A13 was identified as Gram-negative bacteria and had a rods shape. Analysis of 16S rRNA gene sequence showed that isolate A13 had a similarity with Pseudochrobactrum assacharolyticum. Hypersensitivity assay on tobacco leaves showed that isolate A13 was not a pathogen. During 48 hours of incubation, isolate A13 produced a maximum of IAA at the 24th hour of incubation. Isolate A13 produced 0.675 ppm of ethylene/hour in Acetylene Reduction Assay and 69,839 ppm of IAA in HPLC methods. This was the first report on nitrogen fixation and IAA production by Pseudochrobactrum assacharolyticum and its application in the soil of oil palm seedlings. Application of isolate A13 in oil palm seedling increased significantly the number of lateral roots, stem diameter, and height of plants

Analysis of Soil Bacterial Diversity from Tropical Rainforest and Oil Palm Plantation In Jambi, Indonesia by 16S rRNA-DGGE Profiles Risky Hadi wibowo; Nisa Rachmania Mubarik; Iman Rusmana; Maggy Thenawidjaya Suhartono; Sipriyadi Sipriyadi; Masrukhin Masrukhin
Journal of Tropical Biodiversity and Biotechnology Vol 7, No 2 (2022): August
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/jtbb.68820

Oil palm plantations are the most invasive land use changes in Southeast Asia. It must have affected unique natural biodiversity. This study aimed to investigate the diversity of soil bacteria based on 16S rRNA gene profiles from tropical forest and oil palm plantation in Jambi Province, Indonesia. Soil sample was taken from tropical forest and oil palm plantation from Jambi province, Indonesia. The forest site is in Bukit Duabelas National Park, and the nearby oil palm plantation is in Sarolangun District, Jambi Province, Indonesia. The diversity of bacterial communities from topsoil was studied using Denaturing gradient gel electrophoresis (DGGE) of 16S rRNA gene and common biodiversity indices. PCR amplification of 16S rRNA gene was successfully conducted primers-using 33F/ 518R primers. Phylogenetic approach was used for revealing the community shift of bacterial phyla and genera in both areas. Phylogenetic analysis showed there were 4 phyla of bacteria i.e., Firmicutes, Alphaproteobacteria, Gammaproteobacteria, and Actinobacteria, respectively. Actinobacteria was the most dominant group in both areas. The composition of soil bacterial community in the oil palm plantation, based on total number of bands 16S rRNA generated from DGGE was richer than that in the Bukit Dua Belas National Park. It was probably caused by plantation year circle more than 10 years and routine activities during the plantation management, such as applications of agricultural lime, herbicide and fertilizer.

Characterization of Protease from Bacillus licheniformis F11.1 as a Bio-Detergent Agent lmiah, Sitti Nur; Mubarik, Nisa Rachmania; Wahyuntari, Budiasih
Makara Journal of Science Vol. 22, No. 3
Publisher : UI Scholars Hub

Show Abstract | Download Original | Original Source | Check in Google Scholar

Proteases are among the most important enzymes in both food and non-food industries taking up almost 60% of the world enzyme market. This enzyme has been used for many industrial processes, especially in the detergent industry. The purpose of this study was to characterize the protease from Bacillus licheniformis F11.1 as a bio-detergentagent. An enzyme assay of protease activity was used to assess and characterize the protease enzyme from B. licheniformis F11.1. It showed that the highest pH protease activity for alkaline protease occurred at pH 8.0 with a value of 35.00U/mL. Under incubation temperature, the protease had the highest activity at 50 °C with a value of 24.46 U/mL. Protease activity was inhibited by Ca2+,Mn2+, K+, and Na+ions at concentrations of 5 mM. Protease activity can beenhanced by these ions at concentrations of 2 mM. Protease stability can be measured from half-life. Under anincubation temperature of 50 °C, the half-life of the protease at pH 8, 9, and 10 was 108 min, 114 min, and 98 min, respectively. The assay for enzyme stability with an incubation temperature of 60 °C showed half-lives of 92 minutes, 56 minutes, and 61 minutes for pH 6, 9, and 10, respectively. This enzyme was found to be stable with the addition ofdetergent compounds such as sodium dodecyl sulfate (SDS), Triton X-100, ethylenediaminetetraacetic acid (EDTA), and hydrogen peroxide; all under low concentrations. Determination of the molecular weight using SDS-PAGE andzymogram found the molecular weight was 32.90-35.16 kDa. These results showed that the alkaline protease from B.licheniformis F11.1 can be used as a bio-detergent because of its tolerance to various detergent compounds.

Co-Authors , Triadiati . QATRUNNADA Aas Ratnasari Ahmad Suryadi Ainia Hanifitri Alfan Cahyadi Alfaridza, Annisa Nourma ALINA AKHDIYA Andreas Adhi Satya Andreas Adhi Satya ANGELIA REZTY FITRIANI SITUMORANG Anggreandari, Rizky Ani Suryani Ani Suryani Anja Meryandini Antonius Suwanto Aris Tjahjoleksono Aris Tri Wahyudi Atang Sutandi Ayni, Qurrotu Bambang - Riyanto Besty Maranatha BRAMANTYO JATI PRASOJO Budiasih Wahyuntari Budiasih Wahyuntari Budiasih Wahyuntari Cahyadi, Alfan Dadang Suhendar Dadang Suhendar Delfi Trisnawati DERI YURATMOKO Desniar - - Dewi Seswita Zilda Dewi Seswita Zilda Dian Syahfitri Dinamella Wahjuningrum Dwi Ambarawati DWI ANDREAS SANTOSA Ekowati Chasanah Encah Ewi Mulyeti Esti Puspitasari ESTI PUSPITASARI Evi Damayanti Evi Damayanti, Evi Fauzy Rachman Fauzy Rachman Fauzy Rachman Ferymon Mahulette Ferymon Mahulette Ferymon Mahulette, Ferymon Fitratul Aini Fitratul Aini, Fitratul Fitriani Idham Galih Cendana Nabilasani Galih Cendana Nabilasani Hadi Susilo Hamim Hamim Hana Nurullita Prestisia Hasrul Satria Hasrul Satria, Hasrul HENDRA PARDEDE Hirmas Fuady Putra HIRMAS FUADY PUTRA, HIRMAS FUADY Idin Abidin Ika Roostika Tambunan, Ika Roostika Ika Setianingsih, Ika Iman Rusmana Iman, Rusmana Ismi Isti'anah Isna Rahma Dini Iswati, Ruma It Jamilah Ivan Permana Putra Jepri Agung Priyanto Jepri Agung Priyanto, Jepri Agung Karina Eku Dwinanda Gunawan Kusuma Handayani LAKSMI AMBARSARI Lia Siti Nur'amaliyah Lia Siti Nur'amaliyah Lisdar Idwan Sudirman Listyowati, Sri lmiah, Sitti Nur Luky Adrianto Maggy Thenawidjaya Suhartono Maherani, Vincentia Fenice Angger Maranatha, Besty Maria Dita Febriani Lumban Gaol Marini Adani Mashudi Mashudi Maslahah, Iah Novi Masrukhin Masrukhin Muhamad Azwar Syah Mulyorini Rahayuningsih Mutiha Panjaitan Nabilasani, Galih Cendana Nabilasani, Galih Cendana Ninda Ningtyas Nuraliah Rusman Nurfahmi, Riziq Ilham Nurul Hidayati Partomuan Simanjuntak Partomuan Simanjuntak Partomuan Simanjuntak Prayoga SURYADARMA Puspita Lisdiyanti Rika Indri Astuti RIMA ERNIA Risky Hadi Wibowo Risky Hadi wibowo Rizky Anggreandari Rury Eryna Putri Sarah Asih Faulina Sarah Asih Faulina, Sarah Asih Sipriyadi Sipriyadi Sipriyadi Siswa Setyahadi Siswodarsono, Trismilah Siswodarsono, Trismilah Siti Azzira Rahma Sitti Nur Ilmiah Sonya Tobing Sri Budiarti Poerwanto Sri Listyowati Suhendar, Dadang Suhendar, Dadang SYAMSUL BAHRI SYAMSUL BAHRI TEDJA IMAS Thenawidjaya, Maggy Titi Candra Sunarti TRI ASMIRA DAMAYANTI Tri Handayani Kurniati Tri Handayani Kurniati Trismilah Trismilah Siswodarsono Untung Sudadi Wahyu Widosari Wibowo, Risky Hadi Widanarni Widanarni WIDANARNI WIDANARNI Widosari, Wahyu Yoan Ramasita Yusro Nuri Fawzya Zaenal Arifin, Sukarya Zulfarina Zulfarina Zulfarina,

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