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Pipi Deswita
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natural_science@uinib.ac.id
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Prodi Tadris IPA - Fisika FAKULTAS TARBIYAH DAN KEGURUAN UNIVERSITAS ISLAM NEGERI IMAM BONJOL PADANG Jl. Mahmud Yunus Lubuk Lintah Padang
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INDONESIA
Natural Science: Jurnal Penelitian Bidang IPA dan Pendidikan IPA
ISSN : 24776181     EISSN : 2715470X     DOI : -
Core Subject : Science, Education,
Jurnal Natural Science ini memuat artikel yang membahas aspek pendidikan Fisika, metode, model pembelajaran IPA Fisika, inovasi-inovasi pembelajaran, perangkat pembelajaran, dan aspek fisika murni. Tim redaksi menerima artikel ilmiah dari hasil penelitian, laporan studikasus, kajian dan tinjauan pustaka. Terbitnya jurnal pendidikan ini menjadikan suatu indikator bahwa prodi Tadris IPA Fisika sangat peduli terhadap perkembangan dan inovasi-inovasi pada bidang sains terutama pendidikan Fisika. Selain itu adanya Jurnal Natural Science menunjukkan bahwa para dosen Tadris IPA Fisika sudah membudayakan meneliti dan mempublikasikan hasil penelitian. Jurnal studi pendidikan fisika juga mengajak pihak lain berpartisipasi dalam penerbitan jurnal baik universitas local maupun tingkat nasional dan bahkan internasional. Penerbit : Fakultas Tarbiyah dan Keguruan Universitas Islam Negeri Imam Bonjol Padang
Articles 1 Documents
Search results for , issue "Vol 8, No 1 (2022)" : 1 Documents clear
Isolasi dan Identifikasi Molekuler Bakteri Asam Laktat pada Dadih dengan Menggunakan Gen 16S rRNA Alfina Yuliana; Minda Azhar
Natural Science: Jurnal Penelitian Bidang IPA dan Pendidikan IPA Vol 8, No 1 (2022)
Publisher : Universitas Islam Negeri Imam Bonjol Padang

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.15548/nsc.v8i1.3261

Abstract

Dadih is a food product that is naturally fermented from buffalo milk which contains lactid acid bacteria. Determination of the genus or species of bacteria can be identified molecularly. Bacteria can be identified by phenotype and genotype. This study aims to determine the genus or species of lactic acid bacteria in dadih. Identification of lactic acid bacteria was carried out by isolating lactic acid bacteria from the dadih, then isolating the chromosomal DNA of bacterial isolate that had been obtained. Gene of 16S rRNA was amplificated using the Polymerase Chain Reaction (PCR) method with forward BactF1 and reverse UniB1 primers. The PCR amplicon was sequenced using the Dideoxy-Sanger method with a forward BactF1 primer. Sequencing data was read with the BioEdit program. The size of the 16S rRNA gene fragment obtained was 1040 bp. Analysis of the nucleotide base sequence of the 16S rRNA gene fragment showed that the isolate UBC-DTK-02 belonged to the Enterococcus genus and Enterococcus faecalis spesies.

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