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Antibacterial and Antifungal of β-sitosterol Isolated from Hydroid Aglaophenia cupressina Lamoureoux Against Xanthomonas campestris and Fusarium oxysporum

ILMU KELAUTAN: Indonesian Journal of Marine Sciences · Vol. 30 No. 2 (2025) · hlm. 192–202

DOI
10.14710/ik.ijms.30.2.192-202
ISSN
2406-7598, 0853-7291
Terbit
2025-06-15
Penerbit
Marine Science Department Diponegoro University
Bahasa
eng
Lisensi
creativecommons.org/licenses/by-sa/4.0

Abstrak

This study aimed to isolate and characterize β-sitosterol from the marine hydroid Aglaophenia cupressina Lamoureoux and evaluate its antibacterial and antifungal activities against Xanthomonas campestris and Fusarium oxysporum. β-Sitosterol was extracted, purified, and identified using spectroscopic techniques, including infrared and nuclear magnetic resonance spectroscopy. Antimicrobial activity was assessed through agar diffusion method to determine its inhibitory effects on bacterial and fungal growth at varying concentrations. β-sitosterol is a crystalline compound, with a melting point of 138-139°C, consistent with the reported range for pure β-sitosterol, indicating high purity. Infrared (IR) spectroscopy revealed key functional groups, including a hydroxyl group at 3433 cm⁻¹, C-O stretching at 1050 cm⁻¹, and aliphatic hydrocarbon chain vibrations at 2956, 2938, and 2869 cm⁻¹. The C=C stretching at 1634 cm⁻¹ and C-H bending at 1465 cm⁻¹ confirmed its unsaturated sterol structure. ¹H NMR spectroscopy further confirmed the structure with characteristic methyl and olefinic proton signals. The antibacterial activity of β-sitosterol against Xanthomonas campestris showed a concentration- and time-dependent effect, with the highest efficacy observed at 60 ppm, demonstrating potential as a natural antibacterial agent. Additionally, its antifungal activity against Fusarium oxysporum revealed both fungistatic and fungicidal effects, with lower concentrations exhibiting fungistatic behavior and higher concentrations displaying fungicidal activity, thereby offering versatility for both fungal inhibition and eradication. This dual action, combined with its well-characterized molecular structure, positions β-sitosterol as a promising candidate for further development as an antimicrobial compound. The findings underscore the accuracy of the identification process and highlight β-sitosterol's potential in pharmaceutical and agricultural applications, particularly in combating bacterial and fungal infections.

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  • Hasanuddin University
  • National Research and Innovation Agency
  • IPB University
  • Universitas Sulawesi Barat
  • Bandung Institute of Technology
  • Universitas Kristen Indonesia
  • University of Indonesia
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Tampilkan sebagai tabel
Rekan penulisOrganisasiArtikel bersama
Sjafaraenan SjafaraenanHasanuddin University8
Ai HertatiNational Research and Innovation Agency6
Rifqiyah Nur UmamiNational Research and Innovation Agency6
Dody PriosambodoHasanuddin University5
Willem MokaHasanuddin University5
Elis TambaruHasanuddin University5
Nurlaili EkawatiNational Research and Innovation Agency5
Nur HaedarHasanuddin University5
Ambeng AmbengHasanuddin University4
Sheila ChairunnisaNational Research and Innovation Agency4
Jendri MamangkeyUniversitas Kristen Indonesia4
Herman IrawanNational Research and Innovation Agency3
Maritsa NurfatwaNational Research and Innovation Agency3
Ela NoviantiNational Research and Innovation Agency3
Rosana AgusHasanuddin University3
Andi Ilham LatunraHasanuddin University3
Endang SaepudinUniversity of Indonesia3
Bugi Ratno BudiartoNational Research and Innovation Agency3
Anja MeryandiniIPB University3
Baharuddin PatandjengiHasanuddin University2
Asadi AbdullahHasanuddin University2
Anna Ida Sunaryo PurwiyantoSriwijaya University2
Shasmita IrawanNational Research and Innovation Agency2
Moh Egy Rahman FirdausInternational Institute of Molecular Mechanisms and Machines Polish Academy of Science2
Sri SwasthikawatiNational Research and Innovation Agency2
Ratih Asmana NingrumNational Research and Innovation Agency2
Iriani SetyaningsihIPB University2
Zaraswati DwyanaHasanuddin University2
Nenis SardianiHasanuddin University2
Syahribulan SyahribulanHasanuddin University1
Erviana TahirAfiliasi tidak diketahui1
Risco G. BudjiAfiliasi tidak diketahui1
Ilham IlhamCenderawasih University1
Karlina SariAfiliasi tidak diketahui1

Afiliasi berasal dari OpenAlex; metadata OAI-PMH jurnal tidak memuatnya. Penulis tanpa ID OpenAlex dicocokkan berdasarkan nama, sehingga dua orang bisa tergabung atau satu orang bisa terpisah.

Sumber metadata: OAI-PMH (metadata jurnal) http://ejournal.undip.ac.id/index.php/ijms/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-US">Antibacterial and Antifungal of β-sitosterol Isolated from Hydroid Aglaophenia cupressina Lamoureoux Against Xanthomonas campestris and  Fusarium oxysporum</dc:title>
	<dc:creator>Johannes, Eva</dc:creator>
	<dc:creator>Manguntungi, Baso</dc:creator>
	<dc:creator>Tuwo, Mustika</dc:creator>
	<dc:creator>Litaay, Magdalena</dc:creator>
	<dc:creator>Mustopa, Apon Zaenal</dc:creator>
	<dc:creator>Vanggy, Leggina Rezzy</dc:creator>
	<dc:subject xml:lang="en-US">β-sitosterol; Aglaophenia cupressina Lamoureoux; Antibacterial; Antifungal,; Xanthomonas campestris; Fusarium oxysporum</dc:subject>
	<dc:description xml:lang="en-US">This study aimed to isolate and characterize β-sitosterol from the marine hydroid Aglaophenia cupressina Lamoureoux and evaluate its antibacterial and antifungal activities against Xanthomonas campestris and Fusarium oxysporum. β-Sitosterol was extracted, purified, and identified using spectroscopic techniques, including infrared and nuclear magnetic resonance spectroscopy. Antimicrobial activity was assessed through agar diffusion method to determine its inhibitory effects on bacterial and fungal growth at varying concentrations. β-sitosterol is a crystalline compound, with a melting point of 138-139°C, consistent with the reported range for pure β-sitosterol, indicating high purity. Infrared (IR) spectroscopy revealed key functional groups, including a hydroxyl group at 3433 cm⁻¹, C-O stretching at 1050 cm⁻¹, and aliphatic hydrocarbon chain vibrations at 2956, 2938, and 2869 cm⁻¹. The C=C stretching at 1634 cm⁻¹ and C-H bending at 1465 cm⁻¹ confirmed its unsaturated sterol structure. ¹H NMR spectroscopy further confirmed the structure with characteristic methyl and olefinic proton signals. The antibacterial activity of β-sitosterol against Xanthomonas campestris showed a concentration- and time-dependent effect, with the highest efficacy observed at 60 ppm, demonstrating potential as a natural antibacterial agent. Additionally, its antifungal activity against Fusarium oxysporum revealed both fungistatic and fungicidal effects, with lower concentrations exhibiting fungistatic behavior and higher concentrations displaying fungicidal activity, thereby offering versatility for both fungal inhibition and eradication. This dual action, combined with its well-characterized molecular structure, positions β-sitosterol as a promising candidate for further development as an antimicrobial compound. The findings underscore the accuracy of the identification process and highlight β-sitosterol's potential in pharmaceutical and agricultural applications, particularly in combating bacterial and fungal infections.</dc:description>
	<dc:publisher xml:lang="en-US">Marine Science Department Diponegoro University</dc:publisher>
	<dc:date>2025-06-15</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"></dc:type>
	<dc:format>application/pdf</dc:format>
	<dc:identifier>https://ejournal.undip.ac.id/index.php/ijms/article/view/67232</dc:identifier>
	<dc:identifier>10.14710/ik.ijms.30.2.192-202</dc:identifier>
	<dc:source xml:lang="en-US">ILMU KELAUTAN: Indonesian Journal of Marine Sciences; Vol 30, No 2 (2025): Ilmu Kelautan; 192-202</dc:source>
	<dc:source>2406-7598</dc:source>
	<dc:source>0853-7291</dc:source>
	<dc:language>eng</dc:language>
	<dc:relation>https://ejournal.undip.ac.id/index.php/ijms/article/view/67232/pdf</dc:relation>
	<dc:relation>https://ejournal.undip.ac.id/index.php/ijms/article/downloadSuppFile/67232/17795</dc:relation>
	<dc:rights xml:lang="en-US">Copyright (c) 2025 ILMU KELAUTAN: Indonesian Journal of Marine Sciences</dc:rights>
	<dc:rights xml:lang="en-US">https://creativecommons.org/licenses/by-sa/4.0</dc:rights>
</oai_dc:dc>