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Protein Profile and Decolorization Potential of Copper-Resistant Klebsiella pneumonia CKJ 500 2.1.2 in Response to Textile Dyes and Copper

HAYATI Journal of Biosciences · Vol. 33 No. 3 (2026) · hlm. 584–595

DOI
10.4308/hjb.33.3.584-595
ISSN
2086-4094, 1978-3019
Terbit
2026-03-01
Penerbit
Bogor Agricultural University, Indonesia
Bahasa
eng
Lisensi
creativecommons.org/licenses/by-nc/4.0

Abstrak

Heavy metals and synthetic dyes are major environmental pollutants, particularly in industrial effluents. The development of effective and safe bioremediation strategies to mitigate their ecological impact is therefore critical. In this study, the copper-resistant bacterium Klebsiella pneumoniae CKJ 500 2.1.2 was investigated for its capacity to decolorize textile dyes—specifically malachite green—and its associated enzymatic activities were characterized. Bacterial resistance was assessed using Luria–Bertani agar containing varying concentrations of copper and dyes. Decolorization efficiency was evaluated spectrophotometrically, protein expression was analyzed using SDS-PAGE, and dye degradation products were identified using gas chromatography–mass spectrometry (GC-MS). The strain exhibited high tolerance to both copper and dyes, achieving 99.4% decolorization of malachite green and 81% for Congo red. The presence of copper inhibited the decolorization of most dyes, except malachite green and methylene blue. SDS-PAGE analysis identified three key enzymes: laccase (~60 kDa), manganese peroxidase (~39 kDa), and azoreductase (~22 kDa). GC-MS revealed both toxic and non-toxic degradation intermediates, indicating partial detoxification. These findings highlight the potential of K. pneumoniae CKJ 500 2.1.2 for bioremediation of dye-contaminated effluents. However, further research is required to elucidate the complete enzymatic pathways involved and to ensure environmentally safe dye degradation.

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  • Pelita Harapan University
  • The University of Queensland
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Rekan penulisOrganisasiArtikel bersama
Juandy JoPelita Harapan University2
Hans VictorPelita Harapan University2
Deokward F RugaPelita Harapan University1
FigoPelita Harapan University1
Patricia CelineThe University of Queensland1
Melanie CorneliaPelita Harapan University1
Tjie Jan TanPelita Harapan University1
Nathania Calista PutriPelita Harapan University1
Vivian LitantoPelita Harapan University1

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Sumber metadata: OAI-PMH (metadata jurnal) http://journal.ipb.ac.id/index.php/hayati/oai, pertama di-harvest 8 Nov 2026, terakhir terlihat 8 Nov 2026.
Metadata asli (oai_dc)
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	<dc:title xml:lang="en">Protein Profile and Decolorization Potential of Copper-Resistant Klebsiella pneumonia CKJ 500 2.1.2 in Response to Textile Dyes and Copper</dc:title>
	<dc:creator xml:lang="en">Irawati, Wahyu</dc:creator>
	<dc:creator xml:lang="en">Pinontoan, Reinhard </dc:creator>
	<dc:creator xml:lang="en"> Marcellie, Jessica</dc:creator>
	<dc:creator xml:lang="en">Valiant, Andreas </dc:creator>
	<dc:creator xml:lang="en">Sugata, Marcelia </dc:creator>
	<dc:description xml:lang="en">Heavy metals and synthetic dyes are major environmental pollutants, particularly in industrial effluents. The development of effective and safe bioremediation strategies to mitigate their ecological impact is therefore critical. In this study, the copper-resistant bacterium Klebsiella pneumoniae CKJ 500 2.1.2 was investigated for its capacity to decolorize textile dyes—specifically malachite green—and its associated enzymatic activities were characterized. Bacterial resistance was assessed using Luria–Bertani agar containing varying concentrations of copper and dyes. Decolorization efficiency was evaluated spectrophotometrically, protein expression was analyzed using SDS-PAGE, and dye degradation products were identified using gas chromatography–mass spectrometry (GC-MS). The strain exhibited high tolerance to both copper and dyes, achieving 99.4% decolorization of malachite green and 81% for Congo red. The presence of copper inhibited the decolorization of most dyes, except malachite green and methylene blue. SDS-PAGE analysis identified three key enzymes: laccase (~60 kDa), manganese peroxidase (~39 kDa), and azoreductase (~22 kDa). GC-MS revealed both toxic and non-toxic degradation intermediates, indicating partial detoxification. These findings highlight the potential of K. pneumoniae CKJ 500 2.1.2 for bioremediation of dye-contaminated effluents. However, further research is required to elucidate the complete enzymatic pathways involved and to ensure environmentally safe dye degradation.</dc:description>
	<dc:publisher xml:lang="en">Bogor Agricultural University, Indonesia</dc:publisher>
	<dc:date>2026-03-01</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">Peer-reviewed Article</dc:type>
	<dc:format>application/pdf</dc:format>
	<dc:identifier>http://journal.ipb.ac.id/hayati/article/view/67354</dc:identifier>
	<dc:identifier>10.4308/hjb.33.3.584-595</dc:identifier>
	<dc:source xml:lang="en">HAYATI Journal of Biosciences; Vol. 33 No. 3 (2026): May 2026; 584-595</dc:source>
	<dc:source>2086-4094</dc:source>
	<dc:source>1978-3019</dc:source>
	<dc:language>eng</dc:language>
	<dc:relation>http://journal.ipb.ac.id/hayati/article/view/67354/32491</dc:relation>
	<dc:rights xml:lang="en">Copyright (c) 2026 Wahyu Irawati, Reinhard  Pinontoan, Jessica  Marcellie, Andreas  Valiant, Marcelia  Sugata</dc:rights>
	<dc:rights xml:lang="en">https://creativecommons.org/licenses/by-nc/4.0</dc:rights>
</oai_dc:dc>