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Dietary Intake and Accumulation of Phlorotannins in Abalone after Feeding the Phaeophyte Ecklonia stolonifera
Dietary Intake and Accumulation of Phlorotannins in Abalone after Feeding the Phaeophyte Ecklonia stolonifera
Journal of Life Science. 2015. Jul, 25(7): 780-785
Copyright © 2015, Korean Society of Life Science
This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
  • Received : April 06, 2015
  • Accepted : July 23, 2015
  • Published : July 30, 2015
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싸 방구라 이
용기 홍
ykhong@pknu.ac.kr

Abstract
Dietary intake and bioavailability of phorotannins in abalone was investigated after feeding with the phlorotannin-rich brown seaweed Ecklonia stolonifera after 4 days starvation. Reverse-phase high-performance liquid chromatography (RP-HPLC) affords isolation and quantification of the major phlorotannins of 7-phloroeckol and eckol, which were identified by mass spectrometry and nuclear magnetic resonance. Abalone growth and feed consumption rates were similar when fed either with the E. stolonifera or the common feed seaweed Saccharina japonica for 20 days. Throughout the feeding period, 7-phloroeckolol was accumulated in the abalone flesh tissue up to an average of 0.58±0.13 mg/g dry weight after 6 days. Eckol was reached to 0.25±0.05 mg/g dry tissue after 6 days, and maintained the level until end of feeding period. By feeding S. japonica as a control, no phlorotannins were detected in the abalone tissues. Both of the abalone, fed with E. stolonifera or S. japonica , had enzymes that decomposed 7-phloroeckol and eckol in muscle tissues, with similar degradation rates of −0.05 or less and −0.05 mg/ml/hr, respectively. Phlorotannins were reduced by constitutive enzymes in abalone tissues. Therefore, value-added abalone containing bioactive phlorotannins can be produced by simply changing the feed to the phlorotannin-rich brown seaweed E. stolonifera 6 days before harvest.
Keywords
Introduction
Abalone is an herbivorous gastropod feeding mostly on seaweed. It has long been consumed and is a highly valued seafood worldwide. In many countries, abalone is produced by aquaculture. The most important species with regard to aquaculture in Asia is Haliotis discus hannai [5 ]. Annual production levels in Korea in 2013 were estimated to be 7,479 t and 119 t by aquaculture and natural catch, respectively [11] . On-farm production of seaweeds constitutes a viable alternative source for continuous supply of high quality feed [18] . Currently, farmers use to feed their stock of abalone on the locally cultured brown seaweeds Saccharina japonica and Undaria pinnatifida . To render abalone a value-added product, one simple technique would be feeding valuable seaweed containing biologically active compounds. Thus, these substances are transferred to the abalone. In the previous research, bio-active phlorotannins were accumulated in the flesh tissue of abalone by feeding of the Ecklonia cava [1] . Phlorotannins, polymers of phloroglucinol found only in brown seaweeds [14] , are known as potent antioxidant [8] , anti-inflammatory [9] , antidiabetic [13] , and antihypertensive [7] compounds. The Ecklonia stolonifera is also known as a rich source of phlorotannins [6] . This seaweed is common along coastal regions of the South Sea and southern part of East Sea, Korea. It belongs to the family Alariaceae and grows on rocks near and below low-tide mark on rough open coasts. The lamina unifoliate is 0.3-1 m long and 5-30 cm broad [17] . Stipe, 15-25 cm long and 3-5 mm diameter cylindrical, is connected to stolon. The lamina is annual, but the stolon is perennial. The seaweed has bitter and tannin tastes and leathery in texture, thus people prefer not to eat it directly. It is known that polyphenolic substances also deter grazing by abalone [20] . Thus, we assessed the dietary intake and bioavailability of phlorotannins by feeding with the bitter-tasting seaweed after 4 days of starvation. After feeding with the E. stolonifera , amounts of 7-phloroeckol and eckol in abalone tissues, relative growth rates, phlorotannin distribution, and degradation patterns were measured.
Materials and Methods
- Seaweed materials
Feeding material of the brown seaweed Ecklonia stolonifera was collected from the coast of Youngdo (35°08'08'' N,129°04'16''E), Busan, Korea in 2013 and 2014. A voucher specimen was deposited in the author’s laboratory (Y.K. Hong). Seaweed thalli were dried completely for 1 week at room temperature and then stored at 4℃ until feeding. Commercial dry thalli of Saccharina japonica , commonly fed in abalone farms, were used as a reference feed.
- Abalone
The aquacultured abalone Haliotis discus hannai with an initial wet weight of 52±6 g and shell length of 7±1 cm were purchased from the local fish market. They were kept in an aquarium tank (200 l), and acclimatized for 7 days with feeding on S. japonica . Flow-through seawater (3 l/min) was supplied to the tank, and adjusted to 20±1℃. Fecal matter was removed from the tank bottom by siphoning daily, and seawater was renewed at the rate of 30% 1 hr before feeding.
- Feeding trials
Abalone was starved for 4 days before feeding trials. The 6 abalone were kept in each plastic container (10 cm long, 8 cm wide, 5 cm high) with slits on all sides to allow water flow and protect egress of feed. Abalone was fed at a rate of 0.8 g seaweed per one abalone at 17:00 o’clock everyday during feeding trial. To measure the seaweed amount consumed, the thalli remaining after daily feeding were harvested, dried and weighed. Thalli under identical conditions but in the absence of abalone were compared as a control for reasons other than abalone grazing. Feed consumption is expressed as: amount of provided thalli – amount of remained thalli after grazing. Relative growth rate (%) of abalone was calculated as: [(final weight – initial weight) / initial weight)] ×100.
- Quantification of phlorotannins fromE. stolonifera
Phlorotannins were quantified from the seaweed powder according to Chowdhury et al. [3] . Briefly, one gram of powder was suspended in 100 ml of boiling distilled water, and stirred for 5 min to extract water-soluble compounds. For solvent extraction, 10 g of the E. stolonifera powder were shaken in a mixture of methanol (40 ml) and chloroform (80 ml), and then partitioned by adding 30 ml deionized water. The upper layer was collected and extracted again with 30 ml ethyl ether. This crude phlorotannin residue was dissolved in methanol (1 mg/ml) and quantified by reverse-phase high-performance liquid chromatography (RP-HPLC).
- Quantification of phlorotannins from abalone
To measure amounts of 7-phloroeckol and eckol from abalone, tissues detached from the shell were cleaned thoroughly with distilled water to remove contaminants and other mucilage, chopped into small pieces, and ground in paste for 5 min using a hand-held blender. The procedure was conducted on ice to reduce enzymatic degradation of phlorotannins. Phlorotannins were extracted from the tissue paste according to the method of Bangoura et al. [1] . Briefly, abalone paste (2.5 g) was shaken in methanol (10 ml) and chloroforms (40 ml), and then partitioned by adding deionized water (7.5 ml). The upper layer was collected, extracted twice with ethyl ether (7.5 ml), and then dried under nitrogen stream. This crude phlorotannin was dissolved in methanol (300 μl) and quantified by RP-HPLC. The HPLC system included a Waters 486 Tunable Absorbance Detector (Waters Associate Inc., Milford, MA, USA) with a C18 column (250×10 mm; Altech Associates Inc., Deerfield, IL, USA). Elution was performed at a flow rate of 1 ml/min using a linear gradient of 30 to 100% methanol for 40 min. All compounds were isolated on the basis of retention time.
- Identification of phlorotannins
Each substance was analyzed by 1 H nuclear magnetic resonance (NMR) spectroscopy using a JNM-ECP 400 NMR spectrometer (JEOL, Tokyo, Japan) with methanol- d (CD 3 OD). The GC-MS spectrum was analyzed using a GC-MS-QP5050A (Shimadzu, Kyoto, Japan). The chemical structure was verified by comparison with previously reported spectral data [9] .
- Enzymatic degradation of phlorotannins
For the preparation of crude enzyme from abalone tissues, abalone was fed with E. stolonifera or S. japonica for 20 days. The muscle tissue (2.5 g) was ground in 3 ml distilled water, and collected the supernatant enzyme after centrifugation at 3,000 g for 15 min. Crude enzyme (400 μl) was reacted with each pure phlorotannin at 30℃ for 4 hr, and measured periodically the remained amount of each phlorotannin using RP-HPLC. Degradation rates (mg/ml/hr) were calcu-lated by measuring the slope of phlorotannin level according to reaction time.
- Statistical analysis
All data are presented as the mean ± SE of at least three independent replicates. Statistical comparisons of the mean values were performed by analysis of variance (ANOVA), followed by Duncan’s multiple test using the SPSS software (ver. 12.0). Mean values indicated by different letters are statistically significantly different ( p <0.05).
Results
The feeding seaweed of E. stolonifera contains several phlorotannin substances. MS and 1 H-NMR data of major substances revealed that some matched with known phlorotannins and identified their chemical structures. Separation of the water extract (obtained by boiling for 5 min) from E. stolonifera detected major peaks of 7-phloroeckol and eckol by RP-HPLC at retention times of 20 min and 28 min, respectively. Separation of the solvent extract from E. stolonifera detected major peaks of dieckol and phlorofucofuroeckol-A at retention times of 32 min and 39 min, respectively. For comparison of relative growth of abalone fed with phlorotannin-rich E. stolonifera and common fodder S. japonica , each seaweed was fed for 20 days. During the 20-d feeding trial, the relative growth rates of abalone fed with E. stolonifera and S. japonica revealed almost similar ( Fig. 1 ). After abalone adapted to the fodders after 4 days of starvation, their growth rates are reached to approximately 0.7% within 14 days. Thus, the E. stolonifera had no effect on feed preference or growth compared with the common feed seaweed of S. japonica . Total amounts of seaweed consumed by individual abalone during the 20-day feeding period were 1.6±0.2 g for E. stolonifera and 2.4±0.2 g of S. japonica . Daily seaweed consumption of feed was similar, 11% and 15% for E. stolonifera and S. japonica provided, respectively.
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Relative growth rates of abalone after feeding with E. stolonifera and S. japonica. Black circles, E. stolonifera feeding; white circles, S. japonica feeding as a reference. Abalone was fed with 0.8 g seaweed daily. Relative growth rate (%) was calculated as [(final weight – initial weight) / initial weight] ×100. Values are means±SE. Mean values with different letters are significantly different based on Duncan’s multiple range test (p<0.05).
During feeding E. stolonifera to abalone for 20 days, each abalone was removed periodically. The flesh tissue was ground, and the tissue paste (92% moisture) was used to extract phlorotannins. By RP-HPLC, the abalone extract showed two major peaks of 7-phloroeckol and eckol at retention times of 20 min and 28 min, respectively. These substances are water-soluble and were likely partitioned into the aqueous layer because the tissue paste per se had high moisture content. Thus, above phlorotannins were extracted from abalone using a solvent-water partition procedure. Quantification of the compound was calculated based on comparisons of RP-HPLC peak dimensions with those of standard curves. 7-Phloroeckol accumulated to a maximum of 0.58±0.13 mg/g dry weight of abalone tissue after 6 days. The control S. japonica -fed abalone showed no accumulation of this substance ( Fig. 2A ). Eckol reached 0.25±0.05 mg/g dry tissue after 6 days, and accumulated maximum of 0.27±0.08 mg/g dry tissue after 10 days. This eckol level maintained until end of feeding period. Control S. japonica -fed abalone showed no accumulation of eckol ( Fig. 2B ).
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Accumulation of 7-phloroeckol (A) and eckol (B) in abalone flesh after feeding with E. stolonifera. Black circles, E. stolonifera feeding; white circles, S. japonica feeding as a reference. Abalone was fed with 0.8 g of seaweed daily. Phlorotannins accumulated in abalone were quantified by RP-HPLC and expressed as amounts per 1 g of dry flesh tissue. Values are means±SE. Mean values with different letters are significantly different based on Duncan’s multiple range test (p<0.05).
To understand the distribution of phlorotannins in different tissues of abalone, all animals were sacrificed after feeding E. stolonifera (0.8 g/abalone/day) for 6 days, and each of the foot muscle, heart, gonad, and gut tissues was chopped and ground to paste on ice. Table 1 shows the amounts of phlorotannins accumulated in each tissue part. The edible foot muscle tissue contained the highest levels of 7-phloroeckol (0.58±0.13 mg/g dry tissue) and eckol (0.25±0.08 mg/g dry tissue), respectively.
Phlorotannin distributions in abalone tissues after feedingE. stoloniferafor 6 days
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Phlorotannin distributions in abalone tissues after feeding E. stolonifera for 6 days
Levels of both phlorotannins in abalone muscle decreased to zero 5 days later after replacing their food with S. japonica or stopping E. stolonifera feeding. To confirm enzymatic degradation of phlorotannins in abalone tissues, aliquots of muscle paste from abalone fed for 20 days with E. stolonifera or S. japonica (control) were analyzed as enzyme source. Both of the abalone, fed with E. stolonifera or S. japonica , had enzymes that decomposed 7-phloroeckol and eckol in tissues ( Table 2 ). Abalone fed with E. stolonifera showed degradation rates of −0.05 or less and −0.05 mg/ml/hr in the 7-phloroeckol and eckol, respectively. Abalone fed with S. japonica showed degradation rates of −0.03 or less and −0.05 mg/ ml/hr in the 7-phloroeckol and eckol, respectively. S. japonica contained no phlorotannins, but tissue of abalone fed with this fodder could also degrade the phlorotannins. Thus, it seems that the phlorotannin-decomposing enzymes in abalone tissues are a kind of constitutive enzyme.
Enzymatic degradation of phlorotannins by muscle tissues of abalone fed withE. stoloniferaorS. japonica
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Enzymatic degradation of phlorotannins by muscle tissues of abalone fed with E. stolonifera or S. japonica
Discussion
Abalone is a valuable seafood source in many areas of the world where the species is abundant. The foot muscle of abalone is consumed raw or cooked in a variety of dishes, and the shell is used as a decorative item. To produce a value-added abalone with flesh containing biologically active substances, we changed the feed to the brown seaweed E. stolonifera for a short period before harvest. The E. stolonifera contains high levels of diverse phlorotannins [6] , which have diverse biological activities, including anti-oxidative and anti-inflammatory properties [8 , 9] .
Usually, polyphenolic compounds from brown algae are considered to deter grazing by and growth of abalones [20] . Abalones prefer to eat phenolic-poor rather than -rich seaweeds. Humans consume E. stolonifera as a foodstuff after removal of bitter-tasting substances by blanching [10] . Thus, we starved the abalone for 4 days before providing them phenolic-rich E. stolonifera as the sole feed source. After adaptation, abalone consumed this seaweed readily. Significant and similar body weight gain occurred after feeding with phlorotannin-rich E. stolonifera and phlorotanninpoor S. japonica ( Fig. 1 ), indicating that phlorotannins may not affect weight gain, at least during the short 20-day feeding period. Kubanek et al. [12] also reported significant increases in the survival and growth of amphipods upon addition of purified phlorotannins to their feeds. Accumulation of diet-derived substances by many herbivores has been reported. Abalone previously fed with the green seaweed Ulva lactuca accumulated more dimethylsulfoniopropionate than did wild-caught abalone or those that received artificial fodders [16] . The sea hare Aplysia dactylomela grazing on the red seaweed Centroceras clavulatum accumulated mycosporine-like amino acids in the body tissues and spawn [2] . The sea hare grazing on the red seaweed Delisea pulchra accumulated halogenated furanone [4] . The accumulated furanones were lost at a mean rate of −0.92 mg/g dry weight per day from sea hare when fed with Ulva green seaweed [15] .
Common dietary polyphenols undergo extensive degradation in the intestine and liver, facilitating their elimination from the body [19] . Abalone also lost phlorotannins at the same degradation rate of −0.05 mg/ml/hr whether fed with E. stolonifera or S. japonica . It suggests that these phlorotannin-degradable enzymes are expressed constitutively.
In conclusion, the results indicate that E. stolonifera can be used as a fodder source, and that maximum phlorotannin accumulation in abalone flesh occurs after 6 days of feeding. Moreover, our findings suggest the possibility of producing value-added abalone containing high levels of phlorotannins by simply changing the fodder used.
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