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Detection of Plantaricin-Encoding Gene and Its Partial Purification in Lactobacillus plantarum BP102

Jurnal Biodjati · Vol. 8 No. 2 (2023) · hlm. 233–247

DOI
10.15575/biodjati.v8i2.27851
ISSN
2541-4208, 2548-1606
Terbit
2023-11-28
Penerbit
UIN Sunan Gunung Djati Bandung
Bahasa
eng

Abstrak

Lactobacillus plantarum BP102 isolated from garlic bulb tissue has probiotic properties, including producing bacteriocin called plantaricin. This study aimed to detect the gene encoding bacteriocin produced by Lactobacillus plantarum BP102, and to evaluate the bacteriocin activity at each stage of partial purification. After the end of the log phase of L. plantarum BP102 was determined, and the bacteriocin-encoding genes were checked by PCR technique. Partial purification of bacteriocin was elucidated including pH-neutralized cell-free-supernatant (CFS), precipitation using 80% of ammonium sulfate, and dialysis (cut-off 10 kDa), then the bacteriocin activity in every partial purification stage was evaluated. The molecular weight of plantaricin was estimated using SDS-PAGE analysis. Lactobacillus plantarum BP102 harbored the gene encoding plantaricin (pln) biosynthesis, namely plnEF and plnK genes. The activity of crude bacteriocin was inactivated by the presence of proteinase-K enzyme. The protein concentration was gradually decreased along with the purification process. The bacteriocin activity was demonstrated at each step of the purification process (CFS, precipitation, and dialysis) against Bacillus cereus by 9.23 ± 0.20 mm, 7.86 ± 0.15 mm, and 7.6 ± 0.10 mm, respectively; while, Escherichia coli by 10.3 ± 0.55 mm, 7.4 ± 0.1 mm, and 6.86 ± 0.45, respectively. The molecular weight of partially purified bacteriocin BP102 was found to be approximately 15.9 kDa. The overlaid part of the gel showed a slight inhibition against E. coli due to a low protein concentration. This bacteriocin purification process should be further optimized to improve the bacteriocin activity that could be useful for food preservation.

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  • University of Brawijaya
  • Universitas Maarif Hasyim Latif
  • Institut Pertanian Malang
  • Ahi Evran University
  • North Carolina Agricultural and Technical State University
  • Universitas Mulia
  • Universitas Katolik Widya Mandira
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Rekan penulisOrganisasiArtikel bersama
Tri ArdyatiUniversity of Brawijaya3
Muhaimin Rifa’iUniversity of Brawijaya3
Nashi WidodoUniversity of Brawijaya2
Dwi Purno WidekdoUniversity of Brawijaya2
Hikmah MaulidiyahUniversity of Brawijaya2
Salam Adnan IbrahimNorth Carolina Agricultural and Technical State University2
Endang ArisoesilaningsihUniversity of Brawijaya2
Nabila Fitri RosyidaAfiliasi tidak diketahui1
Amin Setyo LeksonoUniversity of Brawijaya1
Anisa ZairinaInstitut Pertanian Malang1
Nia KurniawanUniversity of Brawijaya1
Wildania Putri AgustinaUniversity of Brawijaya1
Marsa SalsabilaUniversity of Brawijaya1
Riska Putri QurotaayuninaUniversity of Brawijaya1
Hakan BozdoğanAhi Evran University1
Agung Putra PurwantoUniversity of Brawijaya1
Alifia Issabella MulyawatiUniversity of Brawijaya1
Suharjono SuharjonoUniversity of Brawijaya1
Evi OctavianyUniversity of Brawijaya1
Dian SiswantoUniversity of Brawijaya1
Idham Halil ZakariaUniversity of Brawijaya1
Siti Mariyah UlfaUniversity of Brawijaya1
Anna SafitriUniversity of Brawijaya1
Nishia Waya MerayUniversitas Mulia1
Rodiyati AzrianingsihUniversity of Brawijaya1
Afifah Nur AiniUniversity of Brawijaya1
Eufrasia R. A. LengurUniversitas Katolik Widya Mandira1
Eko WidodoUniversity of Brawijaya1
Durrotul InayahUniversity of Brawijaya1
Farida RachmawatiUniversity of Brawijaya1
Sri WidyartiUniversity of Brawijaya1
Aris SoewondoUniversity of Brawijaya1
Sri RahayuUniversity of Brawijaya1
Fikriya Novita SariUniversity of Brawijaya1
Sefihara Paramitha SaktiUniversity of Brawijaya1
Catur RetnaningdyahUniversity of Brawijaya1
Viky VidayantiUniversity of Brawijaya1

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Sumber metadata: OAI-PMH (metadata jurnal) https://journal.uinsgd.ac.id/index.php/biodjati/oai, pertama di-harvest 7 Nov 2026, terakhir terlihat 8 Nov 2026.
Metadata asli (oai_dc)
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	<dc:title xml:lang="en-US">Detection of Plantaricin-Encoding Gene and Its Partial Purification in Lactobacillus plantarum BP102</dc:title>
	<dc:creator>Suryani, Elsa Mega</dc:creator>
	<dc:creator>Jatmiko, Yoga Dwi</dc:creator>
	<dc:creator>Mustafa, Irfan</dc:creator>
	<dc:subject xml:lang="en-US">Lactobacillus plantarum</dc:subject>
	<dc:subject xml:lang="en-US">partially purified</dc:subject>
	<dc:subject xml:lang="en-US">plantaricin</dc:subject>
	<dc:subject xml:lang="en-US">precipitation</dc:subject>
	<dc:subject xml:lang="en-US">probiotics</dc:subject>
	<dc:description xml:lang="en-US">Lactobacillus plantarum BP102 isolated from garlic bulb tissue has probiotic properties, including producing bacteriocin called plantaricin. This study aimed to detect the gene encoding bacteriocin produced by Lactobacillus plantarum BP102, and to evaluate the bacteriocin activity at each stage of partial purification. After the end of the log phase of L. plantarum BP102 was determined, and the bacteriocin-encoding genes were checked by PCR technique. Partial purification of bacteriocin was elucidated including pH-neutralized cell-free-supernatant (CFS), precipitation using 80% of ammonium sulfate, and dialysis (cut-off 10 kDa), then the bacteriocin activity in every partial purification stage was evaluated. The molecular weight of plantaricin was estimated using SDS-PAGE analysis. Lactobacillus plantarum BP102 harbored the gene encoding plantaricin (pln) biosynthesis, namely plnEF and plnK genes. The activity of crude bacteriocin was inactivated by the presence of proteinase-K enzyme. The protein concentration was gradually decreased along with the purification process. The bacteriocin activity was demonstrated at each step of the purification process (CFS, precipitation, and dialysis) against Bacillus cereus by 9.23 ± 0.20 mm, 7.86 ± 0.15 mm, and 7.6 ± 0.10 mm, respectively; while, Escherichia coli by 10.3 ± 0.55 mm, 7.4 ± 0.1 mm, and 6.86 ± 0.45, respectively. The molecular weight of partially purified bacteriocin BP102 was found to be approximately 15.9 kDa. The overlaid part of the gel showed a slight inhibition against E. coli due to a low protein concentration. This bacteriocin purification process should be further optimized to improve the bacteriocin activity that could be useful for food preservation.</dc:description>
	<dc:publisher xml:lang="en-US">UIN Sunan Gunung Djati Bandung</dc:publisher>
	<dc:date>2023-11-28</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
	<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
	<dc:type xml:lang="en-US">Peer-reviewed Article</dc:type>
	<dc:format>application/pdf</dc:format>
	<dc:identifier>https://journal.uinsgd.ac.id/index.php/biodjati/article/view/27851</dc:identifier>
	<dc:identifier>10.15575/biodjati.v8i2.27851</dc:identifier>
	<dc:source xml:lang="en-US">Jurnal Biodjati; Vol. 8 No. 2 (2023): November; 233-247</dc:source>
	<dc:source xml:lang="id-ID">Jurnal Biodjati; Vol 8 No 2 (2023): November; 233-247</dc:source>
	<dc:source>2541-4208</dc:source>
	<dc:source>2548-1606</dc:source>
	<dc:language>eng</dc:language>
	<dc:relation>https://journal.uinsgd.ac.id/index.php/biodjati/article/view/27851/9903</dc:relation>
	<dc:rights xml:lang="en-US">Copyright (c) 2023 Jurnal Biodjati</dc:rights>
</oai_dc:dc>