Putra, Masagus Muhammad Prima
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Reduction of Raoultella ornithinolytica TN5 Biofilm using Hot Water and Nanochitosan Fitriani, Khofifah Fajar; Nugraheni , Prihati Sih; Putra, Masagus Muhammad Prima; Puspita, Indun Dewi
Jurnal Ilmiah Perikanan dan Kelautan Vol. 17 No. 3 (2025): JURNAL ILMIAH PERIKANAN DAN KELAUTAN
Publisher : Faculty of Fisheries and Marine Universitas Airlangga

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.20473/jipk.v17i3.74564

Abstract

Graphical Abstract   Highlight Research The biofilm formation of Raoultella ornithinolytica on a stainless steel surface was analyzed Longer duration of hot water immersion leading to a higher reduction of Raoultella ornithinolytica biofilm on stainless steel surface. Longer duration of nanochitosan exposure leading to a higher reduction of Raoultella ornithinolytica biofilm on stainless steel surface The combination treatment of hot water immersion and nanochitosan shows higher efficacy to reduce Raoultella ornithinolytica biofilm on stainless steel surface compare to sodium hypochlorite treatment.     Abstract The equipment surfaces in food processing industries have the potential to contaminate products. Bacteria on a surface are able to form a biofilm. This study aimed to determine the effect of a combination treatment using hot water immersion and nanochitosan on the reduction of R. ornithinolytica’s biofilm on stainless steel surfaces. R. ornithinolytica was applied to a stainless steel surface, incubated at 30oC for 48 hours, and tested for its reduction using hot water immersion treatment with different times. The best result from this treatment was when it was used in combination. The viability of cells was determined using a swab and the total plate count method. A scanning electron microscope was used for qualitative observations of biofilm formed on stainless steel before and after sanitation. The result showed that 10 minutes of hot water immersion resulted in significant R. ornithinolytica biofilm reduction compared to 5 minutes of treatment (p<0.05). Furthermore, the combination treatment of 10 minutes of hot water with 15 minutes of nanochitosan (0.1%) immersion showed the highest percent reduction of R. ornithinolytica biofilm (p<0.05). The ability of the combination treatment to eliminate R. ornithinolytica biofilms is equivalent to or even better than sodium hypochlorite treatment.
Extraction, Purification, and Bioactivity of Fucoxanthin from Brown Seaweed Sargassum hystrix Mufarocha, Nungky; Husni, Amir; Putra, Masagus Muhammad Prima
Jurnal Ilmiah Perikanan dan Kelautan 2026: IN PRESS ISSUE (JUST ACCEPTED MANUSCRIPT, 2026)
Publisher : Faculty of Fisheries and Marine Universitas Airlangga

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Abstract

Graphical Abstract Highlight Research 1. UAE at 45°C for 30 min produced the highest crude extract yield (19.90%). 2. Ethyl acetate:n-butanol (8:2) yielded the highest fucoxanthin fraction (1.31 mg/g). 3. Fucoxanthin fractions showed strong antioxidant activity (DPPH IC₅₀ 86.18±5.06 µg/mL). 4. Purified fractions exhibited strong tyrosinase inhibition (IC₅₀ 76.04±3.24 µg/mL).   Abstract Fucoxanthin is the major carotenoid present in brown seaweeds and exhibits strong biological activities, particularly as an antioxidant and anti-aging agent. However, efficient extraction and purification conditions for fucoxanthin from Sargassum hystrix, along with its functional evaluation, remain limited. This research aimed to establish the most effective extraction conditions for obtaining fucoxanthin from S. hystrix using Ultrasound‑Assisted Extraction (UAE), determine the optimal solvent system for purification, and evaluate the antioxidant and anti-aging activities of both the extracted and purified fucoxanthin. Extraction was carried out using UAE with 96% ethanol at temperatures of 35–45°C and durations of 20–30 min. Purification was conducted through column chromatography using three solvent systems: n‑hexane:acetone (6:4 v/v), methanol:chloroform (7:3 v/v), and ethyl acetate:n‑butanol (8:2 v/v). Fucoxanthin was identified by thin-layer chromatography and fucoxanthin was quantified using reversed-phase high-performance liquid chromatography (HPLC) equipped with a C18 column, while antioxidant activity was measured using the DPPH method and anti-aging activity was assessed via tyrosinase inhibition. The results showed that optimal extraction occurred at 40–45°C for 25–30 min, yielding 18.33–19.9% crude extract, and the ethyl acetate:n‑butanol (8:2 v/v) system produced the highest fucoxanthin fraction yield (8.26–9.54%), with fraction F22 containing the highest fucoxanthin level at 1.31 mg/g. The fucoxanthin fraction displayed markedly enhanced activity, with strong antioxidant capacity (IC₅₀ = 86.18±5.06 μg/mL, an 83.8% improvement over the crude extract) and strong tyrosinase inhibition (IC₅₀ = 76.04±3.24 μg/mL). Overall, fucoxanthin derived from S. hystrix demonstrates substantial promise as an active antioxidant and anti-aging compound for nutraceutical and cosmetic applications, suggesting that future studies should focus on scaling up the extraction and purification process and further elucidating its mechanisms of action and stability in formulated products.