海洋——未来的粮仓     

《山东地质》2009,(9):76-76

在海洋中不能长粮食,怎么能成为未来的粮仓呢？是的,海洋里不能种水稻和小麦,但是,海洋中的鱼和贝类却能够为人类提供滋味鲜美、营养丰富的蛋白食物。蛋白质是构成生物体的最重要的物质,它是生命的基础。现在人类消耗的蛋白质中,由海洋提供的不过5％～10%。20世纪70年代以来,海洋捕鱼量一直徘徊不前,有不少品种已经呈现枯竭现象。  相似文献   

海水产品蛋白质供应量贡献研究          下载免费PDF全文

徐丛春  王晓惠 《海洋开发与管理》2011,28(7):58-63

海洋是人类社会生存和可持续发展的重要物质基础,是人类重要的食品资源基地。文章根据营养与食品安全所提供的食物营养素构成含量,估算了改革开放以来我国海水产品蛋白质的供应量贡献,并与肉类、蛋类及奶类等动物性蛋白质进行了综合比较,为客观评估海水产品对国家粮食安全、居民营养结构与生活质量的贡献提供了量化参考依据。  相似文献   

CO2浓度升高对稻米蛋白质营养品质的影响     

《气象研究与应用》2021,42(z1)

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Detection of the End Point Temperature of Thermal Denatured Protein in Fish and Chicken Meat Through SDS-PAGE Eiectrophoresis     

GAO Hongwei MAO Mao LIANG Chengzhu LIN Chao XIANG Jianhai 《中国海洋大学学报(英文版)》2009,8(1)

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蛋白质营养对高密度养殖凡纳滨对虾生长与免疫力的影响     

夏苏东  李勇  王文琪  于学权  王美琴  王华 《海洋科学》2009,33(5):51-58

在高密度养殖条件下,进行单因素随机设计动物试验.用5种饲料(蛋白质水平31%、35%、39%、43%、47%,以A～E组表示)分别投喂平均体质量6.2 g+0.2 g、平均养殖密度3.1 kg/m3的凡纳滨对虾(Litopenaeus vannamei),探寻蛋白质营养对虾生长、免疫、水质、抗胁迫的影响特征.结果表明:(1)中高蛋白质水平具有显著促进对虾生长的效果,随着蛋白水平的提高,特定生长率先增加后降低,饲料系数正好相反,D组两指标最佳,分另q为110.98%和2.54;C、D、E组差异不显著.(2)中高蛋白质水平有利于提高对虾多数免疫指标的活力,血淋巴中血细胞浓度、T-AOC活力、POD活力、总蛋白含量、白蛋白、血蓝蛋白含量,随着蛋白质水平提高先增加后降低,前5指标含量均以D组最高,比A组显著提高16.8%～33.9%;而血蓝蛋白含量C组最高,比A组提高15.0%.(3)高蛋白质水平有利于提高对虾SOD活力,也显著增强抗低盐胁迫的能力,但同时极显著加大了水环境中氨氮和亚硝氮的污染.(4)在我国北方集约化高密度养殖条件下,凡纳滨对虾中后期生长阶段适宜的饲料蛋白质营养水平为39%～43%.  相似文献   

米氏凯伦藻细胞表面膜蛋白质组及其对温度变化的响应研究     

王坤  王沛  张浩  张树峰  王大志 《海洋与湖沼》2019,50(3):652-663

米氏凯伦藻(Karenia mikimotoi)近年在我国福建、浙江和广东沿海经常形成赤潮,其赤潮不仅影响到海洋生态系统的稳定,也严重威胁到水产养殖以及人类生命健康安全。本论文以米氏凯伦藻为研究对象,建立了米氏凯伦藻细胞表面膜蛋白质荧光标记技术和细胞膜蛋白质提取方法,运用荧光差异凝胶电泳技术(2-DDIGE)对膜蛋白质进行了分析,并研究了米氏凯伦藻的膜蛋白质组及其对环境温度变动的响应。实验共鉴定到44个细胞表面膜蛋白,其中有效注释27个,主要为转运蛋白、HSP70蛋白家族和捕光蛋白等。米氏凯伦藻在20°C条件下的细胞生长和光合作用要明显好于16°C和12°C,但16°C和12°C条件下的差别不大,表明低温限制了米氏凯伦藻的生长。当米氏凯伦藻从12°C快速转移至16°C和20°C时,藻细胞密度和光合作用效率短时间迅速降低,但细胞很快即适应温度变化。细胞膜上的转运蛋白和光合作用蛋白在其适应温度变化中起着重要作用。  相似文献   

White spot syndrome virus envelope protein VP124 involved in the virus infection     

ZHU Yanbing  WU Chenglin  YANG Feng 《海洋学报(英文版)》2008,27(4):130-136

White spot syndrome virus （WSSV） is one of the major shrimp pathogens causing large economic losses to shrimp farming. In an attempt to identify the envelope proteins involved in the virus infection, purified WSSV virions were mixed with three antisera against WSSV envelope proteins （VP39, VP124 and VP187 ）, individually. And then they were injected intramuscularly into crayfish （Procambarus clarkii） to conduct in vivo neutralization assays. The results showed that for groups injected with virions only and groups injected with the mixture of virions and antiserum against VP124, the crayfish mortalities were 100% and 60% on the 8th day postinfection, individually. The virus infection could be delayed or neutralized by antibody against the envelope protein VP124. Quantitative PCR was used to further investigate the influence of three antisera described above on the virus infection. The results showed that the antiserum against VP124 could restrain the propagation of WSSV in crayfish. All of the results suggested that the viral envelope protein VP124 played a role in WSSV infection.  相似文献   

对虾传染性皮下及造血组织坏死病毒衣壳蛋白基因的克隆表达及抗体制备   总被引：2，自引：0，他引：2  

彭小莉  刘棠  徐维佳  王群力  陈伟玲  陈双雅  王景明  谢明星 《台湾海峡》2008,27(1):37-42

本文根据GenBank登录的对虾传染性皮下及造血组织坏死病毒(IHHNV)的全基因组序列(NC-002190),设计出主要结构蛋白基因的相应引物,从厦门发病的对虾中,提取DNA,以此为模板,利用PCR扩增目的基因.再将目的基因分别与pGEX-6p1载体和pET-28a载体连接,构建重组表达载体pGEX-Ⅳ、pET-Ⅳ,重组子经酶切和测序鉴定后导入表达型大肠杆菌BL21,IPTG诱导表达,SDS-PAGE检测,大小约为62KDa和41KDa,与预测大小一致.将pET-Ⅳ表达重组蛋白经纯化,免疫小鼠,Western免疫印迹反应结果表明其抗体均可与pGEX-Ⅳ和pET-Ⅳ表达的蛋白发生特异性反应.本研究的结果为对虾IHHNV的快速检测及其免疫提供了研究基础.  相似文献   

尖刀蛏生化成分和营养价值评价     

吴仁协  苏永全  王军  洪万树  张其永 《台湾海峡》2008,27(1):21-25

分析了尖刀蛏(Cultelles scalprum)肉的生化成分,并对其营养价值进行评定.结果显示:尖刀蛏的含肉率为60.3%,鲜肉中的水分、蛋白质、脂肪和灰分含量分别为84.21%、10.85%、1.31%和1.71%,人体必需氨基酸占氨基酸总量的37.3%,不饱和脂肪酸含量占总脂肪的43.1%,其中廿碳五烯酸(C20:5,EPA)和廿二碳六烯酸(C22:6,DHA)的含量分别占总脂肪的7.8%和15.7%.研究结果表明,尖刀蛏含肉率高,营养丰富,有较高的营养价值和保健价值.  相似文献   

Cloning and sequence analysis of a full-length cDNA of <Emphasis Type="Italic">SmPP1cb</Emphasis> encoding turbot protein phosphatase 1 beta catalytic subunit     

亓飞  郭华荣  王建 《中国海洋湖沼学报》2008,26(1):54-61

Reversible protein phosphorylation, catalyzed by protein kinases and phosphatases, is an important and versatile mechanism by which eukaryotic cells regulate almost all the signaling processes. Protein phosphatase 1 （PP1） is the first and well-characterized member of the protein serine/threonine phosphatase family. In the present study, a full-length cDNA encoding the beta isoform of the catalytic subunit of protein phosphatase l（PPlcb）, was for the first time isolated and sequenced from the skin tissue of flatfish turbot Scophthalmus maximus, designated SmPPlcb, by the rapid amplification of cDNA ends （RACE） technique. The cDNA sequence of SmPPlcb we obtained contains a 984 bp open reading frame （ORF）, flanked by a complete 39 bp 5＇ untranslated region and 462 bp 3＇ untranslated region. The ORF encodes a putative 327 amino acid protein, and the N-terminal section of this protein is highly acidic, Met-Ala-Glu-Gly-Glu-Leu-Asp-Val-Asp, a common feature for PP1 catalytic subunit but absent in protein phosphatase 2B （PP2B）. And its calculated molecular mass is 37 193 Da and pI 5.8. Sequence analysis indicated that, SmPPlcb is extremely conserved in both amino acid and nucleotide acid levels compared with the PPlcb of other vertebrates and invertebrates, and its Kozak motif contained in the 5＇UTR around ATG start codon is GXXAXXGXXATGG, which is different from mammalian in two positions A6 and G3, indicating the possibility of different initiation of translation in turbot, and also the 3＇UTR of SmPPlcb is highly diverse in the sequence similarity and length compared with other animals, especially zebraf＇lsh. The cloning and sequencing of SmPPlcb gene lays a good foundation for the future work on the biological functions of PP1 in the flatfish turbot.  相似文献