Application of Microbial BOD Sensors in Marine Monitoring

A strain of yeast, which can endure high osmotic pressure, is employed for the sensitive material of the microbial BOD sensor. Two immobilization methods are used, I.e. Calcium alginate gel be ads and PV A gel beads. The results show that the PVA gel beads is better. The influences of osmosis and heavy metal ions on the yeast entrapped in the PVA gel beads are also studied in the experiment.     

酶法催化餐饮废油制备生物柴油的研究

以废物资源转化为宗旨,利用固定化脂肪酶催化餐饮废油与乙醇反应制备生物柴油,通过实验获得最佳酯化反应条件:反应温度47℃、有机溶剂为正己烷、醇油比3∶1,5次投加乙醇,酶用量为0.3g,反应时间32h时,生物柴油产率可达81%。     

吸附-交联法固定胰蛋白酶及在澄清啤酒中的应用

胰蛋白酶的固定化采用吸附-交联法.在单因素试验基础上,通过正交试验,获得了胰蛋白酶固定化的最佳条件酶与载体体积比为21,吸附时间为10 h,pH=4.5,缓冲液浓度为0.05 mol/L,戊二醛的质量分数为0.1%.此条件下制得的磁性酶活力回收在50%左右,相对酶活力达74%,该磁性酶对啤酒澄清防止冷浑浊有明显效果.     

坡缕石粘土固定辣根过氧化酶处理硝基酚废水

以坡缕石粘土、淀粉、水玻璃为原料,研究了固定化酶载体的制备工艺,探究了固定化酶载体在辣根过氧化酶(HRP)降解硝基酚废水中的作用,并探讨了反应时间、酶浓度、H2O2及硝基酚浓度对降解效果的影响。结果表明,固定化酶载体的最佳制备工艺为:水玻璃12%,淀粉20%,煅烧温度550℃,煅烧时间2 h;固定化酶对硝基酚的去除效果明显高于原酶;固定化酶去除水中硝基酚的最佳反应条件为:反应时间1.5 h,加酶量150 U,H2O2浓度0.12%,硝基酚浓度100 mg/L;固定化酶重复使用7次后对硝基酚的去除率仍高于60%。     

海藻酸钠凝胶(C_6H_7NaO_6)_x交联Ca~(2+)包埋风味酶的工艺优化及应用稳定性研究

以海藻酸钠为载体,Ca2+为交联剂,对风味酶进行固定化。以固定化酶活力回收率为指标,在单因素试验基础上,通过响应面分析方法优化了固定化风味酶的工艺,并考察了固定化风味酶使用的稳定性。通过对回归模型进行分析,确定最佳的固定化工艺参数为海藻酸钠浓度2.43%,加酶量(酶液体积/海藻酸钠体积)1:1.76,固定化时间2.89 h,此时固定化酶的活力回收率可达81.88%,考虑到实际操作时对参数精度的控制水平,将固定化酶的优化工艺确定为海藻酸钠浓度2.50%,加酶量(酶液体积/海藻酸钠体积)1:2,固定化时间3.00 h,固定化酶的活力回收率达到80.05%±1.33%。优化工艺下制得的固定化风味酶最适使用温度为60?C,热敏感性降低,稳定性提高;最适p H 8.0,比游离酶向碱偏移了1.0,酸碱适用范围增大;可多次使用,冷藏条件下储藏3周后活力依然保持在80%以上。     

固定化微藻对改善养殖水质和增强对虾抗病力的研究

引入固定化波吉卵囊藻(Oocystis borgei)和微绿球藻(Nannochloris oculata)于凡纳对虾(Penaeus vannamei)养殖环境中,检测与凡纳对虾抗病力有关因子的变化和测定主要水质因子,研究固定化微藻改善养殖水质对对虾抗病力的影响。结果表明：引入固定化波吉卵囊藻和微绿球藻的藻珠能改善水质,凡纳对虾的血细胞数目,血清蛋白的含量以及酚氧化酶、溶菌酶、抗菌酶的活性都较对照组显著提高。固定化波吉卵囊藻对氨氮的吸收能力较强,而固定化微绿球藻对亚硝酸盐氮的吸收能力较强。试验期间固定化波吉卵囊藻和微绿球藻的褐藻胶藻珠中的生物量分别增加了约10倍和17倍,证明它们的生理活性不会因固定化而受干扰。因此,固定化微藻可应用于虾池微藻生态调控防病。     

秋冬季环境下固定化氮循环细菌净化湖泊水体氮污染动态模拟

本文依据太湖秋冬季水体氮污染的特点,应用辐射增殖氮循环细胞进行了净化湖水氮污染的动态模拟实验,研究结果表明,富营养化湖水经固定化氮循环净化后,总氮下降７２．４％,氨氮下降８５．６％,出水水质得到明显改善,固定化氮循环细茵在冬季低温（７℃）条件下仍保持了较高的降氮能力,总氮和氨氮去除率分别为５５．６％,５８．９％,降氮效果与湖水滞留时间有关,探讨了固定化氮循环细茵的降氮机理。     

Study on algae removal by immobilized biosystem on sponge

In this study, sponges were used to immobilize domesticated sludge microbes in a limited space, forming an immobilized biosystem capable of algae and microcystins removal. The removal effects on algae, microcystins and UV260 of this biosystem and the mechanism of algae removal were studied. The results showed that active sludge from sewage treatment plants was able to remove algae from a eutrophic lake＇s water after 7 d of domestication. The removal efficiency for algae, organic matter and microcystins increased when the domesticated sludge was immobilized on sponges. When the hydraulic retention time （HRT） was 5h, the removal rates of algae, microcystins and UV260 were 90%, 94.17% and 84%, respectively. The immobilized biosystem consisted mostly of bacteria, the Ciliata and Sarcodina protozoans and the Rotifer metazoans. Algal decomposition by zoogloea bacteria and preyingby microcreatures were the two main modes of algal removal, which occurred in two steps： first, absorption by the zoogloea; second, decomposition by the zoogloea bacteria and the predacity of the microcreatures.     

固定化生物技术在合成染料废水处理中的应用

在多级折流板反应器生物处理装置中,采用活性炭为载体人工固定化生物处理合成染料废水,出水水质稳定, 出水中的烷烃肽链变短;其对COD_Cr和BOD₅的去除率可达96.46%、99.77% ;对SO^2-₄和钙镁总量的去除效率超过80.37%、78.66%;折流板反应器的容积负荷率N_v可达2.8 kg COD/(d•m³)。活性炭经生物固定化后,不仅不会影响它的处理效果,还会延长活性炭的使用寿命;当冲击性有机负荷发生时,固定化生物活性炭能够承受并能很快恢复。     

Purification and Refolding of a Novel β-Agarase from Inclusion Body of E. coli

β-agarase AgaB appears to represent a new family of glycoside hydrolase; it is structurally and functionally different from other known agarases. In the present study, AgaB was expressed with a temperature-inducible expression system in E. coli BL21 (DE3) as a fusion protein bearing a C-terminal hexahistidine tag. The protein existed mainly in the form of inclusion body.After being washed and solubilized, AgaB in inclusion body was denatured and purified to electrophoretic purity by immobilized metal affinity chromatography. The purified AgaB was then refolded using a simple pulse dilution method, and the refolded AgaB showed a high specific hydrolysis activity of about 1600 units/mg protein. Forty milligrams of refolded pure protein were obtained from 1L of culture.