Nalinanon, Sitthipong

Preferred name

Alternative Name

Nalinanon, S.

Nalinanon, Sittipong

Main Affiliation

School of Food Industry

sitthipong.na@kmitl.ac.th

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Lipid oxidation and fishy odour development in protein hydrolysate from Nile tilapia (Oreochromis niloticus) muscle as affected by freshness and antioxidants
(2012-06-15)
Yarnpakdee, Suthasinee
;
Benjakul, Soottawat
;
Nalinanon, Sitthipong
;
Kristinsson, Hordur G.
Lipid oxidation and fishy odour development in protein hydrolysate from fresh and ice-stored Nile tilapia (Oreochromis niloticus) were investigated. During iced storage of 18 days, heme iron content decreased with a concomitant increase in non-heme iron content (P < 0.05). Peroxide value (PV) and thiobarbituric acid reactive substances (TBARS) values increased. Phospholipid content decreased with a corresponding increase in free fatty acid content. The results suggested that lipid hydrolysis and oxidation took place during storage. When protein hydrolysates were produced from fresh and 18 days ice-stored Nile tilapia muscle, higher lipid oxidation and fishy odour/flavour along with higher amount volatile compounds were obtained in hydrolysate for unfresh sample (P < 0.05). However, the addition of mixed antioxidants during hydrolysis process markedly lowered lipid oxidation, b ·, ΔC ·, ΔE · values, fishy odour/flavour as well as the formation of volatile compounds in the resulting hydrolysates prepared from both fresh and unfresh samples. Therefore, hydrolysate from Nile tilapia muscle with reduced fishy odour and lighter colour could be prepared by using fresh fish and incorporation of mixed antioxidants during hydrolysis. © 2011 Elsevier Ltd. All rights reserved.
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Autolysis of clown featherback (Chitala ornata) muscle
(2019-01-01)
Thiabmak, Chompunutch
;
Sriket, Chodsana
;
Yarnpakdee, Suthasinee
;
Kim, Siriporn Riebroy
;
Nalinanon, Sitthipong
Clown featherback (Chitala ornata) is a freshwater fish important in the cuisine of Thailand and other Southeast Asian countries. It has a short marketable life due mainly to poor gelling characteristic even when stored in ice. This deterioration has been associated with muscle autolysis. The research was aimed to investigate the autolysis of clown featherback muscle (CFM). To test autolysis, mince from CFM was incubated in a temperature controlled water bath for 60 min at 5, 10, 20, 30, 40, 50, 60, 65, 70, 75 or 80 °C at pH levels over the range of 2-11. The results showed that the highest autolytic activity was at 70 °C and it occurred at pH levels of 4 and 7, with pH 4 showing the highest autolysis. CFM was incubated with its crude enzyme counterpart at the physiological pH (6.73) at both 4 °C and 25 °C. Degradation of natural actomyosin showed that after incubation at either temperature myosin heavy chain was susceptible to hydrolysis indicating that autolysis of CFM took place even at low temperature as affected by its endogenous proteases. The effects of several protease inhibitors were tested and autolysis at the physiological pH (6.73) was strongly inhibited by 10 μM pepstatin A (20.3% inhibition), which had significantly higher inhibitory activity (P < 0.05) among the protease inhibitors tested. This suggests that aspartic protease was the major proteinase in CFM.
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Characteristic and antioxidant activity of Cladophora glomerata ethanolic extract as affected by prior chlorophyll removal and drying methods
(2022-08-01)
Yarnpakdee, Suthasinee
;
Senphan, Theeraphol
;
Wangtueai, Sutee
;
Jaisan, Chalalai
;
Nalinanon, Sitthipong
Impact of prior chlorophyll removal (PCR) and drying methods (freeze- and oven-drying) on characteristics and antioxidant activities of the ethanolic extracts (EEs) from Cladophora (C.) glomerata, freshwater macroalgae, were investigated. The extraction yields were found in the range of 7.18%–13.15% with total phenolic (TPC) and total chlorophyll (TCC) contents of 19.40–25.69 mg GAE/g dry extract and 3.58–7.94 mg/g dry extract, respectively. Yield, TPC and TCC decreased when dechlorophyllization was implemented before extraction, regardless of drying method (p ≤.05). Increase in L* value with coincidental decrease in ΔE* value was observed in the EE with PCR. Freeze-dried EE with PCR (FEE-PCR) showed greater antioxidant efficiencies (both in vitro and oxidation model systems) than that oven-dried EE with PCR (p ≤.05). Liquid chromatography/mass spectrometry (LC/MS) analysis indicated that quercetin-3-O-glucoside was the most abundant phenolic compounds identified in the FEE-PCR. Therefore, freeze drying in combination with PCR was effective preparation method to maximize antioxidant activity and improve color of EE. Practical applications: Lipid oxidation is one of important reactions affected on the deterioration of food quality and safety. Many antioxidants have been widely used to retard lipid oxidation. Due to their health hazard of synthetic antioxidants, the search for safer ingredients with potent antioxidant activity resources is attracted interest. Phenolic compounds, the bioactive substances distributed in aquatic plants, have been known as antioxidant with health benefit. However, chlorophyll associated algal extract influenced on color and bioactivity of phenolic compound, which limits its utility. Moreover, drying technologies also have an impact on a stability of active components in algal sample. To maximize the utility of alga, the appropriate pretreatments by chlorophyll removal along with effective drying method could be a better choice for preservation of bioactive compounds. As a consequence, a wider application can be achieved. The corresponding extracts could therefore be used as an alternative natural antioxidant for food applications, instead of synthetics in a future.
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Elucidating the physicochemical and structural properties of Ganoderma lucidum spores: Comparative analysis of various disruption techniques
(2024-04-15)
Sriket, Chodsana
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Kuimalee, Surasak
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Yarnpakdee, Suthasinee
;
Benjakul, Soottawat
;
Sriket, Pornpimol
This study evaluated Ganoderma lucidum G2 spores (GLS) using various processing techniques: vibrating milling, ball milling, and autoclaving. Broken GLS via vibrating and ball milling showed higher lipid content (22.89% and 22.50%) but lower L*, a*, and b* values compared to intact GLS. Vibrating milling achieved the highest sporoderm-broken rate (98.27%). Ball milling resulted in the highest lipid oxidation. Vibrating milling yielded the highest bioactive compounds, and both methods increased DPPH-RSA values. Differential scanning calorimetry indicated varying T<inf>max</inf> values: non-broken GLS (106.56 °C), vibrating milling (92.77 °C), ball milling (97.58 °C), and autoclaving (109.35 °C). FT-IR spectra showed triterpenes, polysaccharides, and fatty acids. X-ray diffraction and Fourier transform infrared spectroscopy revealed increased crystallinity with vibrating milling (37.12% to 47.99%). Both milling methods altered GLS structure to a disintegrated, pancake-like form. Scanning electron microscopy with energy-dispersive X-ray spectroscopy indicated significant carbon and oxygen concentrations. This study provided crucial insights for utilizing GLS.
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Physicochemical characteristics of glucosamine from blue swimming crab (Portunus pelagicus) shell prepared by acid hydrolysis
(2018-12-01)
Kraisangsri, Jittrakan
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Nalinanon, Sitthipong
;
Riebroy, Siriporn
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Yarnpakdee, Suthasinee
;
Ganesan, Palanivel
The aim of this research was to characterize glucosamine hydrochloride (GluHCl) from the shell of blue swimming crab (Portunus pelagicus). The crab shell was finely milled and processed to chitin prior to HCl hydrolysis using 30 % HCl for 30 min at 100 ºC for glucosamine production. The resultant glucosamine was recovered by crystallization using 95 % ethanol and was dried in a hot air oven. The color of the glucosamine crystals, expressed as L*, a*, and b*, was 83.01, 5.03, and-3.38, respectively. Crab shell glucosamine had high purity, which could be strongly stained by ninhydrin and presented at the same Rf of standard D-glucosamine using thin layer chromatography. Furthermore, prepared glucosamine exhibited similar Fourier transform infrared (FTIR) spectrum as standard D-glucosamine. Glucosamine from blue swimming crab shell had high purity as determined by HPLC and contained 808.15 mg D-glucosamine/g sample. The maximal transition temperature (T<inf>max</inf>) and the total enthalpy (ΔH) of prepared glucosamine were 194 ºC and 754.42 J/g, respectively. As a consequence, with the presented method, the resultant glucosamine was characterized to be D-glucosamine. Therefore, blue swimming crab shell, a byproduct from crab meat processing, has high potential as a raw material to produce glucosamine for food and nutraceutical applications.

Nalinanon, Sitthipong

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