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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) · pp. 192–202

DOI
10.14710/ik.ijms.30.2.192-202
ISSN
2406-7598, 0853-7291
Published
2025-06-15
Publisher
Marine Science Department Diponegoro University
Language
eng
License
creativecommons.org/licenses/by-sa/4.0

Abstract

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.

Keywords

Collaboration network of the authors

40 authors · 158 co-authorship links · showing the 40 most connected

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Co-authorOrganisationJoint articles
Herman IrawanAffiliation unknown6
Ai HertatiAffiliation unknown6
Nurlaili EkawatiAffiliation unknown5
Willem MokaAffiliation unknown4
Rifqiyah Nur UmamiAffiliation unknown4
Sheila ChairunnisaAffiliation unknown4
Jendri MamangkeyAffiliation unknown4
Dody PriosambodoAffiliation unknown3
Maritsa NurfatwaAffiliation unknown3
Ela NoviantiAffiliation unknown3
Elis TambaruAffiliation unknown3
Bugi Ratno BudiartoAffiliation unknown3
Anja MeryandiniAffiliation unknown3
Ariandi AriandiAffiliation unknown3
Resti Ura’Affiliation unknown2
Anna Ida Sunaryo PurwiyantoAffiliation unknown2
Shasmita IrawanAffiliation unknown2
Moh Egy Rahman FirdausAffiliation unknown2
Sri SwasthikawatiAffiliation unknown2
Ratih Asmana NingrumAffiliation unknown2
Muhammad RaihanAffiliation unknown1
SubehanAffiliation unknown1
HabibieAffiliation unknown1
Nurhasni HasanAffiliation unknown1
Sitti Nur FatimahAffiliation unknown1
AnugerahAffiliation unknown1
Jabal Rahmat HaedarAffiliation unknown1
Crisnawati CrisnawatiAffiliation unknown1
Dody PrisambodoAffiliation unknown1
Slamet SantosoAffiliation unknown1
Marwa DevianaAffiliation unknown1
Ulfah Nur AmaliahAffiliation unknown1
Munif S HasanAffiliation unknown1
Nur Ramaliani SamsulAffiliation unknown1

Affiliations come from OpenAlex; journal OAI-PMH metadata carries none. Authors without an OpenAlex ID are matched by name, which can merge or split people.

Metadata source: OAI-PMH (metadata jurnal) http://ejournal.undip.ac.id/index.php/ijms/oai, first harvested 8 Nov 2026, last seen 8 Nov 2026.
Original metadata (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>
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	<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>