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海带膳食纤维的提取与功能性试验 总被引：2，自引：1，他引：2
采用酶技术和化学处理相结合的方法 ,研究了海带膳食纤维的工艺技术 ,筛选出海带膳食纤维提取和漂白的最佳工艺条件 ,提取出海带膳食纤维产品 ,并进行人体的功能性试验。结果表明 ,海带膳食纤维的产率达 2 7.3% ,颜色为类白色 ,膳食纤维含量达 73.3% ,钙含量 7.5% ,膨胀力为55m L/ g,持水力为 2 650 % ;海带膳食纤维的功能性优于小麦麸皮膳食纤维 ,对便秘患者具有良好的疗效。 相似文献
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溶藻弧菌(Vibrio alginolyticus)是水产养殖中致病性较强的一种条件致病菌,为更灵敏、高效地对其进行检测,研发出一种基于核酸适配体竞争置换作用的检测方法。首先设计并制备出磁珠-核酸适配体-荧光报告探针的检测复合物(MAP检测复合物),然后利用溶藻弧菌与其核酸适配体有较好的亲和特异性,在对样品进行检测时,样品中的溶藻弧菌就会竞争MAP检测复合物中的核酸适配体,从而置换出与该核酸适配体结合的荧光报告探针,再通过检测置换出的报告探针的荧光强度来表征溶藻弧菌的浓度,从而实现对溶藻弧菌的定量检测。结果表明,该方法对溶藻弧菌的检测限可达到1CFU/mL,与嗜水气单胞菌(Aeromonas hydrophila)、迟钝爱德华氏菌(Edwardsiella tarda)、哈维氏弧菌(Vibrio harveyi)、大肠杆菌(Escherichia coli)等水产养殖中的常见致病微生物没有交叉反应,并在1~20、20~100和100~1000 CFU/mL范围内都表现出较好的线性关系。另外还对MAP检测复合物的制备条件进行了优化,较为理想的制备条件为:100nmol/L核酸适配体与100nmol/L荧光报告探针按体积比1︰1混合结合30 min,制备出50 nmol/L的核酸适配体-荧光报告探针复合物,然后该复合物再与25μg/mL的磁珠按体积比1︰1混合结合60 min,制备出相应的MAP检测复合物。利用核酸适配体的竞争置换作用检测溶藻弧菌有较好的灵敏度和特异性,展现了较好的应用前景。 相似文献
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以浒苔(Enteromorpha prolifera)为原料,采用响应面法优化碱性过氧化氢提取半纤维素的条件。在单因素实验的基础上,运用Box-Benhnken中心组合原理,设计四因素三水平实验,确定半纤维素最佳提取条件。采用红外光谱(FT-IR)和离子色谱(IC)分析浒苔半纤维素组分。结果表明,各因素对浒苔半纤维的提取率的影响为:时间温度料液比氢氧化钠浓度。碱性过氧化氢法提取半纤维素的最佳条件为:氢氧化钠浓度为4.8 g/L,提取温度为92℃,提取时间为5 h,料液比1︰70,半纤维素的提取率为56.75%,与预测值57.30%基本一致。FT-IR结果显示,浒苔半纤维素红外吸收光谱中含有明显的木糖和阿拉伯糖的特征吸收峰,为吡喃环结构,由β-糖苷键连接。离子色谱结果表明,浒苔半纤维素主要由木糖和阿拉伯糖组成,含有少量葡萄糖和半乳糖。木糖含量为54.4%,其次为阿拉伯糖,含量为15.3%,葡萄糖和半乳糖含量分别为5.6%和2.7%。 相似文献
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毛细管气相色谱法测定海带提取多糖中的L-褐藻糖含量 总被引：1，自引：0，他引：1
建立快速而准确灵敏的方法测定海带(Laminaria japonica)提取多糖——褐藻多糖硫酸酯中的L,褐藻糖含量。海带多糖经酸解后,转化成糖腈乙酸酯衍生物。采用SGEAC225毛细管柱进行分离,实验中以肌醇为内标物。从青岛产海带提取的褐藻多糖硫酸酯中仅含有L,褐藻糖和I)-半乳糖2种单糖,样品10-1,10-2,10-3,1阻4中的L褐藻糖的平均含量分别为32．9072％,32．3147％,31．2924％,32．3571％,回收率为97．1％～99．9％,变异系数为0．23％～0．60％。采用气相色谱法测定海带多糖中的L褐藻糖含量准确、可靠。 相似文献
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海带中细胞激动素的纯化分离方法 总被引：1，自引：0，他引：1
海带样品于 2 0 0 1年采自青岛太平角海湾 ,用三种不同方法处理样品 ,通过对实验方法及条件的筛选 ,确立了提取、纯化和分离海带中细胞激动素的方法步骤和流程。结果表明 ,最佳方法的基本步骤为 :( 1 )用甲醇∶水∶醋酸 ( 70∶ 30∶ 3,V/V/V)从海带组织中提取出细胞激动素 ,再用PVPP柱去除提取液中的酚类和其他杂质 ;( 2 )将提取液通过连在一起的PVPP柱、DEAE柱和C1 8柱 ,以纯化样品并同时从自由基、核苷、核苷酸和葡糖苷型细胞激动素混合物中分离出核苷酸型细胞激动素 ;( 3)用接有氨基柱的正相液相色谱进一步将葡糖苷型细胞激动素分离出来 ;( 4 )用C1 8液相色谱柱分离其他各种细胞激动素 相似文献
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目的：通过星点设计-效应面法优选壮药盘龙止咳颗粒的最佳提取工艺,为后续研发更有效、更稳定、更方便的新制剂提供依据。方法：采用高效液相色谱法进行含量测定,采用单因素试验、星点设计-效应面法考察乙醇浓度、溶剂倍量、提取时间及提取次数,以山奈酚-3-O-龙胆二糖苷与岩白菜素总含量及干膏率的综合评分为评价指标,优选出壮药盘龙止咳颗粒最佳提取参数。结果：壮药盘龙止咳颗粒的最佳提取工艺为加入12倍量浓度为50%的乙醇,每次提取50 min,提取2次。结论：通过星点设计-效应面法优选盘龙止咳颗粒的提取工艺,方法预测性良好,重复性良好,简便可靠,为改变服用剂型研究提供了可靠依据。 相似文献
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叶绿素荧光遥感算法为探测近岸海域二类水体叶绿素浓度开辟了新途径．基于大连湾及邻近海域的实测数据,本文研究了海水叶绿素浓度的荧光遥感算法．结果表明：随着海水叶绿素质量浓度的增高,荧光峰出现显著的红移现象,叶绿素质量浓度与荧光峰波长存在着正相关关系．此外,基于MODIS、MERIS及GLI传感器荧光波段建立的荧光基线高度算法较差,不适用于该研究海域．选择680、685、690、695、700、705nm作为荧光峰波长建立的荧光基线高度算法,随着选定波长的增大,该算法拟合的相关性逐渐增高,最大相关系数（R2）可达0．91;而以实测荧光峰波长建立的荧光基线高度算法最佳,乘幂函数拟合优于线性拟合,拟合方程为P（chl）=3．167×10^5 FLH^1.45（R2=0．93）．本研究为新一代海洋水色卫星传感器的开发、建造提供了科学依据,并为已有高光谱传感器在叶绿素荧光遥感反演方面的应用打下了基础． 相似文献
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A cartridge of solid phase extraction (SPE), hydrophilic–lipophilic balance (HLB), has been used to enrich phosphomolybdenum blue (PMB) from water samples without any other additives. Based on this, the previous on-line SPE method established for the determination of nanomolar soluble reactive phosphorus (SRP) in seawater has been greatly improved. Cetyltrimethylammonium bromide (CTAB), the cationic surfactant needed for the formation of the PMB-CTAB paired compound that could be extracted on a Sep-Pak C18 cartridge using the previous method [Liang, Y., Yuan, D.X., Li, Q.L., Lin, Q.M., 2007. Flow injection analysis of nanomolar level orthophosphate in seawater with solid phase enrichment and colorimetric detection. Marine Chemistry 103, 122–130.], was not necessary. Thus the longer time and higher temperature required for the complete formation of the PMB-CTAB compound were no longer needed. In addition, with application of the sequential injection analysis technique the proposed method showed the advantages of being much faster, simpler, sample and reagent saving, as well as more convenient in operation. The PMB compound formed under room temperature was efficiently extracted on an in-line HLB cartridge, rapidly eluted by 0.15 mol/L NaOH solution, and finally determined with a laboratory-made spectrophotometer at 740 nm. Experimental parameters, including the volume of reagents added, sample loading flow rate, and eluting flow rate, were optimized. Time and temperature for the PMB reaction, and salinity effect were also studied, and these were found to have no severe effect on the detection. With variation of sample loading time at a fixed flow rate, a broadened determination range of 3.4 to 1134 nmol/L phosphate could be obtained. The recovery and the method detection limit of the proposed method were found to be 94.4% and 1.4 nmol/L, respectively. The relative standard deviation (n = 7) was 2.50% for the sample at a concentration of 31 nmol/L phosphate. Two typical seawater samples were analyzed with both the proposed method and the magnesium hydroxide-induced coprecipitation method and, using the t-test, the results of the two methods showed no significant difference. 相似文献
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采用阳极溶出伏安法(ASV)对1999年10月采自浙江省三门湾健跳港表层海水中溶解态铅的形态进行了分析,结果表明:海水中游离态铅的浓度为2.2 nmol/dm3,有机配位态则可分为两类,即PbL1和PbL2;两类有机配位体条件稳定常数的对数(logKpcobnLd1,pb2 和logKpcobnLd2,pb2 )分别为8.4和9.1;两类有机配位体浓度(L1和L2)分别为37.4 nmol/dm3和52.7 nmol/dm3,将上述结果与以往三门湾海区研究中海洋生物急性毒性试验结果和不同介质中铅含量进行对比可知,浙江三门湾健跳港海区表层海水中溶解态铅浓度对海洋生物是安全的,但个别底栖生物物种中较高的铅含量已影响到人类的食用安全。 相似文献
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日本真海带对硒的积累和生物转化 总被引：4，自引：0，他引：4
在海水中添加亚硒酸盐(Na2SeO3)及不同浓度的氮磷营养盐(NaNO3+NaHO2PO4),研究海带对硒的积累,通过分离测定海带富硒前后各生化组分的含硒量来探讨硒的生物转化问题.结果表明天然海带含硒量(鲜重)为0.451~0.596μg/g,海带富硒最佳的Na2SeO3浓度为200mg/dm3,培养56h后的富硒倍率约为50.在天然海带中,硒主要以有机态存在,有机硒占总硒含量的86.22%;在含有200mg/dm3NaO2SeO3的海水中培养56h后测得海带的总硒为24.481μg/g,其中有机硒含量为16.703μg/g,无机硒为4.714μg/g;在添加氮磷营养盐的含硒海水中,海带的富硒能力得到进一步的提高,在适宜的氮磷条件下(150mg/dm3NaNO3和25mg/dm3NaHO2PO4)总硒含量达到33.649μg/g,而无机硒含量基本不变,为4.497μg/g,因此提高部分转化为有机硒,有机硒含量达到24.678μg/g.这说明海带具有通过自身代谢将无机硒转化为有机硒的较强的能力. 相似文献
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《Marine Chemistry》2007,103(1-2):122-130
Phosphomolybdenum blue (PMB) paired with cetyltrimethylammonium bromide (CTAB) can be extracted using a solid phase extraction technique on C18 sorbent. Based on this, a novel on-line solid phase extraction method coupled with flow injection (FI) analysis and colorimetric detection has been established to determine nanomolar level orthophosphate in seawater. A stopped flow technique was employed to assure the complete formation of the PMB–CTAB compound, which was sequentially extracted on an in-line Sep-Pak C18 cartridge. The adsorbed PMB–CTAB can be rapidly eluted by 0.56 mol/L H2SO4 in ethanol, and determined with a spectrophotometer at 700 nm. Experimental parameters, including reaction temperature, sample loading flow rate, stopped time and eluting flow rate, were optimized throughout the experiments based on univariate experimental design. The results show that reaction temperature and stopped time were the major factors affecting the formation of PMB–CTAB. Silicate concentration up to 5000 times higher than that of orthophosphate would not interfere with the determination of orthophosphate. Using artificial seawater with salinity of 35 as a matrix under the optimized conditions, the standard curve shows a linear range between 3.2 and 48.5 nmol/L, and the recovery and the detection limit of the proposed method are 96.4% and 1.57 nmol/L, respectively. The relative standard deviation (RSD) (n = 8), which was determined daily for 8 days, was 4.52% for the artificial seawater at a concentration of 32.4 nmol/L orthophosphate. Two typical seawater samples were analyzed using both the proposed method and the MAGnesium hydroxide-Induced Coprecipitation (MAGIC) method. The results of the two methods show no significant difference using the t test. Compared to the MAGIC method, the proposed method has the advantage of being more sensitive, faster, sample saving and easy for on-line analysis. 相似文献
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研制出一种对溶解氧敏感的传感膜,其荧光材料主要是邻菲咯啉钌。由光源发出的中心波长为465 nm的强光照射到铺有该络合物的膜片上,激发出中心波长为620 nm的荧光,水体中的溶解氧会对激发出的荧光产生猝灭效应,猝灭程度与溶解氧的质量浓度之间存在线性关系。该膜片在无氧水中的荧光强度是空气饱和水中的20倍,变化较为明显。对比检测荧光信号在待测水体中猝灭前后的强度,即可测出水体中溶解氧的质量浓度。基于这一原理和荧光测量技术研制了光学溶解氧分析仪,利用该仪器对6处不同水域的天然水体进行测试,所得测试结果与国标碘量法的测试结果之间不存在显著性差异,误差≤2%,响应时间<1 min。在海水中30 m深处进行36h稳定性考察,所得溶解氧质量浓度数值平均偏差小于0.2 mg.L-1,证实仪器可适应较为恶劣的环境,且稳定性较好。 相似文献