50DE微囊营养强化轮虫DHA的研究↑（*）

应用５０ＤＥ微囊ＤＨＡ营养强化饵料强化轮虫试验，结果表明：试验Ａ、Ｂ两区强化６小时后轮虫ＤＨＡ／ＦＡ含量由最初的未检出上升为１．５％、４．０％，１２小时后达到最高峰，分别为７．５％和１０．３％、而对照Ｃ区在２４小时试验区间ＤＨＡ均未检出。     

不同饵料对中华绒螯蟹幼体发育和存活的影响

采用高度不饱和脂肪酸（ＨＵＦＡ）营养强化的轮虫、轮虫与卤虫组织投喂中华绒螯蟹幼体,以各项幼体的存活率为评判指标,对不同饵料及其组合的投喂效果进行了探讨。研究结果表明：轮虫是中华绒螯解早期幼体（Ⅰ、Ⅱ期）的适口饵料,幼体存活率随轮虫密度的增加而逐渐上升,但当轮虫数量超过最适密度时,幼体存活率反而有所下降。其中,未强化的轮虫达投喂密度为６０ｉｎｄ．ｍＬ＾－１,强化轮虫最适密度为４０ｉｎｄ．ｍＬ＾－１。Ｚａｏ状Ⅰ、Ⅱ期投喂４０ｉｎｄ．ｍＬ＾－１轮虫,从Ⅲ期开始投喂１０ｉｎｇ．ｍＬ＾－１卤虫无节幼体,能较好地满足中华绒螯蟹幼体发育的营养需求,提高大眼幼体的存活率。表明强化幼体饵料ＨＵＦＡ特别是ＥＰＡ和ＤＨＡ能有效地促进幼体的发育与存活和脱壳率。     

真鲷幼鱼的EPA,DHA需求量研究

通过向真鲷幼鱼饵料中分别添加０．２％、０．５％和１％的ＥＰＡ、ＤＨＡ以及两种混合脂肪酸，以豆油为基础脂肪源研究真鲷幼鱼的ＥＰＡ、ＤＨＡ的需求量。结果表明，饵料中缺乏ＥＰＡ、ＤＨＡ时，真鲷幼鱼生长缓慢，成活率仅达６５％，随着ＥＰＡ在饵料中的添加，幼鱼的成活率与增重率都有所增加。     

轮虫强化培养的研究进展

轮虫是海水鱼虾类苗种生产中的重要开口饵料。目前使用的轮虫主要有Ｂｒａｃｈｉｏｎｕｓｐｌｉｃａｔｉｌｉｓ(Ｌ型 )和Ｂ .ｒｏｔｕｎｄｃｆｏｒｍｉｓ (Ｓ型 )两种。由于海产小球藻等单细胞藻类的繁殖速度小于轮虫的摄食量 ,在大规模轮虫培养中单胞藻不能满足需要 ,制约了轮虫的生产。用酵母和含高度不饱和脂肪酸 (ＨＵＦＡ)的人工饵料是替代单胞藻最常用的办法〔1、2〕,但其必需脂肪酸 (ＥＦＡ)缺乏或不足 ,用作轮虫的饵料前需进行ＥＦＡ的强化〔3〕。目前 ,轮虫培养在ＥＦＡ强化、替代饵料、高密度培养、冷冻藻保存利用和休眠卵利用等…     

ω_3HUFA对中华绒螯蟹幼体存活率及体脂肪酸组成的影响

分别以经海水小球藻、牟氏角毛藻和５０ＤＥ－Ｇ强化剂强化的轮虫投喂中华绒螯蟹早期幼体,至Ｚａｏ状Ⅲ期后改喂卤虫无节幼体,探讨了饵料ω－３系列高度不饱和脂肪酸对幼体发育和存活的影响。结果表明：小球藻轮虫组的幼体发育至第Ⅰ期幼蟹的存活率最高,为１２．００％,强化剂轮虫组和角毛藻轮虫组次之,分别为１０．６７％和９．６７％,而酵母轮虫组最低,仅为３．６７％;结合分析Ｚａｏ状Ⅴ期幼体脂肪酸组成可知,幼体发育至第Ⅰ期幼蟹的存活率与其总脂含量和ω－３ＨＵＦＡ含量密切相关,而Ｚａｏ状Ⅴ期幼体总脂含量与ω－３ＨＵＦＡ含量随饵料轮虫总脂和ω－３ＨＵＦＡ含量的增加而提高,表明早期幼体所摄取的ω－３ＨＵＦＡ对后期幼体发育和存活有明显的促进作用。     

微藻EPA和DHA的研究现状及前景

高度不饱和脂肪酸 (ＰＵＦＡ)在营养和医学上的重要作用 ,已引起人们广泛的兴趣 ,特别是二十碳五烯酸 (ＥＰＡ)和二十二碳六烯酸 (ＤＨＡ)两者对防治心脏疾病、动脉硬化、癌症、风湿关节炎、气喘和糖尿病等人类疾病有明显效果[1～ 3 ] ,已成为研究开发的热点。在水产上 ,ＥＰＡ和ＤＨＡ是许多鱼类幼体、对虾幼体、双壳类幼虫的必需脂肪酸 ,关系到幼虫和幼体的生长发育和存活。ＥＰＡ和ＤＨＡ虽然对有些动物不是必需的 ,但在饵料中适当添加这些物质 ,可提高投喂动物的生长速度和存活率[4～ 6] 。目前国内外对微藻中的ＥＰＡ和ＤＨＡ已进行了…     

不同喂养条件下蒙古裸腹溲脂肪酸组成比较

比较不同食物和不同处理方式培养的蒙古裸腹溲脂肪酸组成，ＥＰＡ含量在用海水小球藻全培养时为２７．６％，用２种面包酵母培养的分别为５．６％和１０．７％，用鱼油强化的为７．４％和１０．５％。试验表明蒙古裸腹溲难以同化吸收食物中的ＤＨＡ，但在鱼油强化时其肠道中储存的油粒可含一定量的ＤＨＡ，因此可用ＤＨＡ含量高的鱼油短时间强化，以肠道为ＤＨＡ载体，来满足海水鱼苗的营养要求。     

不同喂养条件下蒙古裸腹溞脂肪酸组成比较

比较不同食物和不同处理方式培养的蒙古裸腹（Ｍｏｉｎａｍｏｎｇｏｌｉｃａ）脂肪酸组成，ＥＰＡ含量在用海水小球藻全培养时为２７．６％，用２种面包酵母培养的分别为５．６％和１０．７％，用鱼油强化的为７．４％和１０．５％。试验表明蒙古裸腹难以同化吸收食物中的ＤＨＡ，但在鱼油强化时其肠道中储存的油粒可含一定量的ＤＨＡ，因此可用ＤＨＡ含量高的鱼油短时间强化，以肠道为ＤＨＡ载体，来满足海水鱼苗的营养要求。     

稚鱼生物饵料的DHA营养强化

综述了国内外海水稚鱼生物饵的ＤＨＡ营养强化技术研究及其应用状况，轮虫、卤虫的营养强化方法和注意事项。     

海水仔稚鱼对脂类的需求

脂类是海水仔稚鱼的必需营养要素，ｎ－３高度不饱和脂肪酸是海水仔稚鱼的必需脂肪酸，能直接影响海水仔稚鱼的生长和存活，其中又以ＤＨＡ和ＥＰＡ尤为重要。在仔稚鱼饵料中添加磷脂，也可提高仔稚鱼的生长和存活率。     

Supercritical CO<Subscript>2</Subscript> extraction and concentration of n−3 polyunsaturated fatty acid ethyl esters from tuna cooking juice

Cooking is an important step in the tuna canning process; it usually produces functional solubilized proteins and lipids. The objective of this study was to recover and increase the concentration of functional n−3 fatty acids from the lipids in cooking juice. The lipids contained 12.98% eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) after ethyl esterification and increased to 37.4% with subsequent urea adduct fractionation. Supercritical carbon dioxide extraction was further used to increase the concentration of EPA and DHA ethyl esters. The ratio of EPA+DHA ethyl esters (high-molecular-weight components) to that of C₁₆ and C_18∶1 fatty acid ethyl esters (low-molecular-weight components) was used as a separation index for evaluating the process variables. Experimental results indicated that a high CO₂ density caused a low separation factor. At 1500 psig and 328.2 K, the extraction collected over 600 L CO₂, displaying an accepted concentration factor of EPA+DHA ethyl esters herein. About 80% yield of EPA and DHA was obtained and the ethyl esters increased from 37.4% to 54.3%.     

鸡粪浆及5种微藻对轮虫脂肪酸组成的影响

采用投喂鸡粪浆的方法培养轮虫,并与5种微藻培养轮虫的脂肪酸组成进行了比较。结果表明:鸡粪轮虫具有较高的营养价值,HUFA含量达25.9%,仅次于小球藻轮虫和新月菱形藻轮虫,EPA和DHA的含量分别为11.2%和4.4%;在5种微藻培养的轮虫中,用小球藻、新月菱形藻和球等鞭金藻培养的轮虫营养价值较高,而用微绿球藻和衣藻培养的轮虫营养价值相对较低;轮虫的脂肪酸组成受饵料影响显著,但又不完全取决于饵料。     

锯缘青蟹幼体饵料的营养强化

用酵母、水球藻、鱼油强化和豆油强化四种不同方式培养轮虫，再分别投喂锯缘青蟹幼体，分析测定轮虫和体的生化组成，结果显示，（1）不同方式培养的轮虫之间以及摄食这些轮虫的锯缘青蟹幼体之间的蛋白质含量都没有显著差异；（2）轮虫的脂类含量和脂肪酸组成与培养方式密切相关，小球藻轮虫的脂类含量最高，20：5n-3(EPA)占总脂肪酸的比例也最高 ，为18.05%，鱼油轮虫则含有最多的22：6n-3(DHA)，占总脂肪酸3.16%，脂类含量仅次于小球藻轮虫；（3）锯缘青蟹幼体的脂类含量和脂肪酸组成受相应饵料营养成分的影响。另外，幼体培育实验也发现，饵料营养成分影响幼体的存活率，结果表明，提高轮虫的EPA和DHA含量，尤其晨DHA含量，将有利于锯缘青蟹幼体的存活和发育。     

Biochemical composition and fatty acid profile in a strain of the lineage ‘Nevada’, belonging to the Brachionus plicatilis (Rotifera) complex,fed different diets

A strain of the lineage Brachionus ‘Nevada’ was batch cultured with two diets, differing in biochemical composition: baker's yeast (treatment 1), which has higher protein:lipid ratio compared with CULTURE SELCO (treatment 2). The biochemical composition (DNA, RNA, lipid, protein content) and fatty acid profile of rotifers of both treatments was analysed and related to previously published population structure data. CULTURE SELCO‐fed rotifers showed higher DNA, RNA, lipid, n‐3 highly unsaturated fatty acids (HUFA) average content, compared with yeast‐fed rotifers, which had higher protein content. Rotifer lipid content showed significant diurnal variation in yeast‐fed rotifers. Rotifer lipid and n‐3 HUFA content was associated with reproductive output. DNA and RNA content was related to embryonic development while protein content, to somatic growth and mixis. The saturated and monounsaturated fatty acid rotifer content was stable irrespective of feed, in contrast to eicosapentanoic acid (EPA) and DHA. The levels of AA were similar in both rotifer populations, but those of EPA and docosahexaenoic acid (DHA) were about half in yeast‐fed compared with CULTURE SELCO‐fed rotifers. CULTURE SELCO resulted in a temporally stable rotifer lipid profile and a better enriched parthenogenetic population.     

Effect of short- and long-term lipid enrichment on total lipids,lipid class and fatty acid composition in rotifers

Four emulsions differing in lipid class composition: triacylglycerols, ethyl esters, phospholipids and wax esters were used to enrich rotifers either through short-term (ST) enrichment (24 h) or through long-term (LT) enrichment (10 days). Higher lipid levels were obtained by using the ST enrichment method. This was particularly marked in the high triacylglycerol accumulation in rotifers enriched on the phospholipid-based emulsion. Ethyl esters were effectively assimilated and incorporated into triacylglycerol by rotifers in both the ST and LT techniques. A high docosaehexanoic/eicosapentaenoic acid (DHA/EPA) ratio was obtained in the LT technique using the ethyl ester-based emulsion. However, the other emulsion treatments gave higher or equal DHA/ EPA ratios using the ST technique. Absolute phospholipid levels were independent of both dietary lipid composition and enrichment method used, whereas triacylglycerol levels depended on these parameters. During starvation the level of phospholipid, in absolute terms, decreased slightly whereas the triacylglycerol fraction decreased considerably. Rotifers enriched on the wax ester-based emulsion using the LT technique exhibited higher levels of long-chain monoenes (i.e. 20:1 and 22:1 isomers) than when the ST technique was used. This suggests that hydrolysis of the wax esters and oxidation of the liberated fatty alcohols to fatty acids occurred when the LT technique was applied.     

Optimizing the essential fatty acids, eicosapentaenoic and docosahexaenoic acid, in the diet of the prawn, Penaeus monodon

The dietary requirements of Penaeus monodon for eicosapentaenoic (20:5n‐3; EPA) and docosahexaenoic (22:6n‐3; DHA) acids were examined. These requirements were examined when dietary levels of linoleic (18:2n‐6; LOA) and linolenic acids (18:3n‐3; LNA) were also provided at previously established optimal levels of 14 and 21% respectively of the total lipid fatty acids. A 5 × 5 factorial design was used with incremental amounts (0, 4, 8, 12 and 16% of total fatty acids) of EPA and/or DHA. An additional diet containing cod‐liver oil was provided as a reference diet. The total lipid content of all of the 25 treatments and reference diets was maintained at the same level of 75 g kg^?1. Growth of prawns fed with the reference diet after 50 days was 244 ± 21%. The greatest response to singular additions of EPA or DHA was with a 12% inclusion of either fatty acid, resulting in 287 ± 21 and 293 ± 18% weight gain, respectively. Growth was generally better when combinations of EPA and DHA were used, the optimal combination being EPA 4% and DHA 4%, resulting in 335 ± 25% weight gain. Addition of high levels of either of the highly unsaturated fatty acids (HUFA) in the diet had a negative effect on growth. Digestibilities of the total neutral lipid and specific fatty acids were examined during the growth trials. The digestibility of total neutral lipid was usually higher when either or both HUFA were present, however there were few significant differences between treatments that contained either or both HUFA. Following the growth trials, digestive glands (DG) of prawns fed with the various diets were analysed to determine the total lipid content and fatty acid composition. Total lipid in the digestive gland increased with the inclusion of DHA, but was not significantly affected by the addition of EPA. The fatty acid composition of the digestive gland lipid generally reflected that of the diet. However, the maximum retention of EPA (11.1% of total DG fatty acids) and DHA (10.7% of total DG fatty acids), was not directly proportional to the amount of either fatty acid present in the diet. These results demonstrate that both EPA and DHA have considerable growth promoting capacity. This growth promoting capacity is enhanced when an optimal balance of both fatty acids are incorporated into the diet.     

Enrichment of Rotifers Brachionus plicatilis with Eicosapentaenoic Acid and Docosahexaenoic Acid Produced by Bacteria

Abstract— Two bacterial strains, rich in either eicosapentaenoic acid [EPA, 20:5(n-3)] ( Shewanella gel-idimarina ACAM 456) or docosahexaenoic acid [DHA, 22:6(n-3)] ( Colwellia psychroeryrhrus ACAM 605) were tested for their ability to enrich rotifers Erachionus plicatilis in these polyunsaturated fatty acids. Rotifers were exposed for 24 h to each bacterial strain and to a mixture of the two strains. They were then harvested and their fatty acid compositions were analysed and compared to those of rotifers that had been either starved or fed yeast Saccharomyces cerevisiae or microalgae Tetraselmis suecica in 2-L glass flasks. Exposure to 1.4 × 10⁹ cells/ml of the EPA-producing bacterium only resulted in rotifer EPA levels increasing from 0.1% to 1.2% of total dry weight (%dw). Similarly, following exposure to 1.0 × 10⁹ cells/mL of the DHA-producing bacterium only, rotifer DHA levels increased from below detection to 0.1% dw. When exposed to a mixture of the two bacterial strains, containing 7.0 × 10⁸ celldml of the EPA producer and 5.0 × 10⁸ cells/mL of the DHA producer, the rotifers'final EPA and DHA levels were 0.5% dw and 0.3% dw respectively. Although feeding strategies need refining, these results show, for the first time, that rotifers can be enriched with DHA from bacteria, and that rotifers can be enriched simultaneously with both DHA and EPA from different bacterial strains.     

Effects of dietary lipids on the fatty acid composition of triglycerides and phospholipids in tissues of white sturgeon

Eight purified diets were fed to juvenile white sturgeon, Acipenser transmontanus Rick, for 9 weeks to investigate the effect of dietary lipids on the fatty acid composition of phospholipids and triglycerides from muscle, liver and brain. The diets contained 150 g kg^?1 of oils from canola, corn, cod liver, lard, linseed, soybean, safflower, or a control mixture (corn oil/cod liver oil/lard, 1:1:1, by wt). Dietary lipids significantly (P≤ 05) affected the composition of tissue triglycerides and phospholipids. Tissue triglyceride fatty acid composition ranged widely, in parallel with the dietary lipids, while phospholipids changes were more conservative. Brain phospholipid fatty acid composition was less responsive to diet compared with that in muscle and liver. Considerable amounts of n-6 and n-3 long chain polyun-saturated fatty acids (> C₂₀) were found in triglycerides and phospholipids with all diets, demonstrating that white sturgeon can desaturate and elongate linoleic acid (18:2n–6) and linolenic acid (18:3n–3). Further, the products of the Δ6 desaturase, i.e. 18:3 n–6 and 18:4n–3, were relatively abundant in triglyceride, suggesting that the Δ6 desaturase might not be a limiting step in the process in white sturgeon. Nevertheless, accumulation of both EPA and DHA was greater in the sturgeon fed fish oil than those fed linseed oil, indicating that muscle triglyceride EPA and DHA levels are best enhanced by diets rich in preformed EPA and DHA.     

Optimization of emulsion properties and enrichment conditions used in live prey enrichment

Five variables relating to the enrichment of live prey were studied using experimental micellar emulsions. Rotifers and Artemia nauplii were enriched for 12 and 24 hrs, respectively, and sampled at several intervals to analyse their fatty acid profile and determine the better time length for enrichment. Two hour and 18 hr were shown to be the most effective in boosting rotifer and nauplii, respectively, with arachidonic (ARA), eicosapentaenoic (EPA) and docosahexaenoic (DHA) fatty acids as well as in total lipid content. Three doses of the same emulsion were also used to check which one conferred the best fatty acid profile. In this case, the higher the dose utilized the higher the content of DHA present in the live food. The use of 15 g/Kg–20 g/Kg of egg yolk as emulsifier was proved to be very effective on rotifer boosting, whereas for nauplii, the amount of emulsifier might be reduced. Egg‐derived emulsifiers have been shown to be more effective for rotifer enrichment while for Artemia nauplii, soy lecithin rendered a better fatty acid profile. Finally, live prey lipid composition paralleled that of the oil used in the emulsion formula although rotifers were far more easily enriched than Artemia nauplii especially in DHA but not in EPA or ARA.     

Oil from Calanus finmarchicus—Composition and Possible Use: A Review

The long-chain omega-3 fatty acids eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) are produced by phytoplankton in the marine food web. Zooplankton acts as an important link between phytoplankton and fish at higher trophic levels and may therefore be a potential source for these fatty acids. The copepod Calanus finmarchicus is a lipid-rich zooplankton present in large amounts in the North Atlantic Ocean. The astaxanthin-rich oil contains 80–90 % wax esters consisting of mainly long-chain monounsaturated fatty alcohols esterified to saturated or unsaturated fatty acids. The long-chain n-3 fatty acids may account for 20–30% of the fatty acids in the wax esters. The wax ester rich oil is well utilized by fish, and the history of utilization, safety, and tolerability of wax esters for humans are being addressed. Recent reports indicate that oil from C. finmarchicus may have beneficial health effects beyond those which may be ascribed to intake of EPA and DHA alone.