Amplification and Analysis of Rbcl Gene (Ribulose-1,5-Bisphosphate Carboxylase) of Clove in Ternate Island

International Conference on Life Sciences and Technology

Nurhasanah^1 ; Sundari^1 ; Papuangan, Nurmaya^1

Study Program of Biology Education, Faculty of Teacher Training and Education, Khairun University Ternate, Indonesia^1

关键词: 5-bisphosphate;    clove;    DNA barcoding;    DNA extraction;    Plant species;    Precise position;    rbcL;    Ternate;   

Others  :  https://iopscience.iop.org/article/10.1088/1755-1315/276/1/012061/pdf
DOI  :  10.1088/1755-1315/276/1/012061

来源: IOP

【 摘 要 】

DNA Barcoding is recommended as a tool for identifying and confirming species within the taxonomy framework. The rbcL gene is the barcode DNA for plant species. Ternate Island is one of clove plantation center in North Maluku. The diversity and productivity of cloves on the Ternate island known since in earlier times. This study has a purpose to amplify the rbcL gene in clove plants collected from clove plantations of communities in Ternate island. Isolation of total DNA carried out with using ZymoBiomic (Zymo Research DNA Extraction) Kit from leaves tissue, then DNA specimen is amplified based on rbcL gene with forwarding sequence rbcLaF 5′-ATG TCA CCA CAA ACA GAG ACT AAA GC-3′ and reverse sequence is rbcLaR 5′-GTA AAA TCA AGT CCA CCR CG-3′. The results showed that the specimen was successfully amplified with an amplicon size of 600 bp. Furthermore, BLASTN analysis results note that the sequence has a similarity of 99% with Syzygium cumini vc. J.R. Abbott 23676 (FLAS) ribulose-1,5-bisphosphate carboxylase large subunit (rbcL) gene, but phylogenetically the precise position of sample could not found because the limitation of rbcL gene.