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Isolasi dan Identifikasi Molekuler Bakteri Pelarut Fosfat dari Gua Gamelan di Kawasan karst Kiskendo Kendal, Jawa Tengah

*Hawari Rosdiana Mahmudah  -  Laboratorium Bioteknologi, Departemen Biologi, Fakultas Sains dan Matematika, Universitas Diponegoro| Universitas Diponegoro, Indonesia
Agung Suprihadi  -  Laboratorium Bioteknologi, Departemen Biologi, Fakultas Sains dan Matematika, Universitas Diponegoro| Universitas Diponegoro, Indonesia
Anto Budiharjo  -  Laboratorium Bioteknologi, Departemen Biologi, Fakultas Sains dan Matematika, Universitas Diponegoro| Universitas Diponegoro, Indonesia

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Abstract

Phosphate solubilizing bacteria is a group of bacteria that dissolves unavailable phosphate into the form that can be absorbed by plants. This research aimed at isolation and moleculer identification of phosphate solubilizing bacteria based on 16s rRNA from bat cave guano and potential microorganisms which were able to dissolved phosphate. Several stages of this research are, isolation PSB in Pikovskayaand NBRIP agar, Gram staining, and molecularidentification. The isolation result obtained two isolates phosphate solubilizing bacteria, which are G4-1 and G5. Isolate G5 is the highest on solubilizing phosphate with a diameter of clear zone 22.01 mm, and Isolate G4-1 exhibited diameter of clear zone 19.8 mm. Isolates G4-1 and G5 are the gram-negative bacteria. DNA amplification of these bacteria employing universal primers 27 F (5’-AGAGTTTGATCMTGGCTCAG-3’) dan Primer 1492 R (5’-GGTTACCTTGTTACGACTT-3’) generated the 1520 bp and 1235 bp PCR product. The result of the analysis of 16s rRNA gene sequence showed that isolate G4-1 has 80% similarity with Acinetobacteriwofii strain-JCM partial sequence, and isolate G5 has 92% similarity with Serratia marcesens strain-NBRC.

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  1. Barrow, G.I. & R.K.A Feltham. 1993. Cowan and Steel Manual for the Identification of Medical Bacteria. New York : Cambridge University Press
  2. Clarridge JE. 2004. Impact of 16s rRNA gene sequence analysis for identification of bacterial on clinical microbiology and infectious diseases. ClinMicrobiol Rev 17:840-862
  3. Doughari, Hamuel J., Patrick Alois Ndakidemi.,Izanne Susan Human., Spinney Benade. 2011. The ecology, bilogy, and pathogenesis of Acinetobacter spp.: an overview, Microbes and Environtment, Applied Sciences Faculty, Cape Penisula
  4. University Of Technology, South Africa
  5. Ginting, R.C.B., R. Saraswati dan E. Husen. 2006. Mikroorganisme Pelarut Fosfat. Dalam Simanungkalit, R.D.M., Suriadikarta, D.A., Saraswati, R., Setyorim, D., dan Hartatik, W. Pupuk Organik dan Pupuk Hayati. Selected reading, hlm. 141-158. Balai Besar Litbang Sumber daya Lahan Pertanian. Bogor
  6. Illmer, P., Barbato, A., and Schinner, F. 1995. Solubilization of Hardly-Soluble AlPO4 with P-solubilizing Microorganisms. Soil Biol.Biochem. 27:265-270
  7. James, J., C. Baker, H. Swain. 2008. Prinsip- prinsip sains untuk keperawatan. Erlangga, Jakarta
  8. Janda, J.M. and S. L. Abbott. 2007. 16s rRNA gene sequencing for bacterial identifications in the diagnostic laboratories: Pluses, perils, and pitfalls. J. Clinic Microbiol. 45(9):2761-2761
  9. Lemey, P., M. Salemi & A.M. Vandamme. 2009. The Phylogenetic Handbook: A Practical Approach to Phylogenetic Analysis and Hypothesis Testing. Cambridge University Press. UK
  10. Mohan, M., G. Selvakumar, S.N. Sushil, J.C. 2011. Entomopathogeneticity of endophytic Serratia marcescens Strain SRM against larvae of Helicoverpaarmigera (Noctuidae: Lepidoptera). World J. Microbiol. Biotechnol. Published online 07 april 2011
  11. Musapa, M., T .Kumwenda, M. Mkulama, S. Chishimba, D. E. Noris, P. E. Thuma, dan S. Mharakurwa. 2013. A simple chelex protocol for DNA extraction from Anopheles spp. J. Vis. Exp. 71: 1- 7
  12. Osborne, C. A., M. Galic, P. Sangwan, dan P
  13. H. Jansen. 2005. PCR generated artifact from 16S rRNA gene-specific primers. FEMS Microbiol. Lett. 248: 183-187
  14. Sambrook J, Fritsch EF, Maniatis T. 1989. Molecular cloning : a laboratory manual. Second Edition. CSH Centennial
  15. Setiawati, M. R. & Pranoto, E. 2015. Perbandingan Beberapa Bakteri Pelarut Fosfat Eksogen pada Tanah Andisol sebagai areal Pertanaman Teh Dominan di Indonesia. Jurnal Penelitian Teh dan Kina 8(2): 158-
  16. Simanungkalit, R. D. M dan Suriadikarta, D
  17. A. 2006. Pupuk Organik dan Pupuk Hayati. Balai Besar Litbang Sumberdaya Lahan Pertanian. Bogor. Situmorang, E. C., Prameswara, A. S. H. C., Mathius, N. T. & Liwan, T. 2015. Indigenous Phospate Solubilizing Bacteria from Peat Soil Solé, M.,
  18. Francia A., Rius, N., & Lorén, J. G. 1997. The Role of pH in The “Glucose Effect” on Prodigiosin Production by Non-proliferating Cells of Serratia marcescens. Lett Appl Microbiol. 25: 81–84
  19. SWOFFORD, D.L., G.J. OLSEN., P.J. WADDELL and D.M. HILLS. 1996
  20. Phylogenetic inference. In: Molecular Systematics, 2nd Edition. HILLS, D.M., C. MORITZ and B.K. MABLE
  21. (Eds.) Sinauer Associates, Sunderland, Massachusetts. Chap. 5
  22. pp. 407 – 514
  23. Widawati S & Suliasih. 2006. Populasi Bakteri Pelarut P (BPF) di Cikini, Gunung Botol dan Ciptarasa serta Kemampuannya dalam melarutkan P Terikat di Media Pikovskaya Padat. Jurnal Biodiversitas. 7 (2) : 109 –
  24. Widyati E. 2007. Formulasi inokulum Mikroba: MA, BPF dan Rhizobium Asal Lahan Bekas Tambang Batubara untuk Bibit Acacia crassicarpa Cunn. Ex-Benth. Jurnal Biodiversitas 8 (3) :
  25. - 241
  26. Yukimasa N, Takeshi I, Hiroshi I. 1988. Acinetobacter radioresistens sp. nov. isolated from cotton and soil. Int J Syst Bacteriol. 38(2): 209-211

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