投加FeSO4对序批式生物膜反应器中DHA、EPS和处理效果的影响

针对化学协同生物除磷过程,研究了序批式生物膜反应器(SBBR)中FeSO_4对悬浮相活性污泥脱氢酶活性(DHA)、胞外聚合物(EPS)及系统处理效果的影响.结果表明,少量FeSO_4对DHA和EPS的分泌具有促进作用,但最佳投加量不一致,分别为0.10 mmol·L-1和0.20 mmol·L-1;大量的FeSO_4则会引发抑制.FeSO_4投加量少于0.30 mmol·L-1时会使污泥MLVSS、MLVSS/MLSS增加,超过0.30 mmol·L-1时则使MLVSS、MLVSS/MLSS下降,但MLSS和SVI随着FeSO_4投加量的增加分别持续增加和下降.FeSO_4对COD和TN的去除具有抑制作用,但并不显著,去除率分别在77%和72%左右;TP的去除效果明显改善,在投加量为0.30 mmol·L-1时效果最好.投加FeSO_4协同生物除磷时建议最佳投加量为0.30 mmol·L-1,此时污泥DHA被轻微抑制,但污泥浓度、EPS、TP去除率均已达到最大,出水水质满足一级A排放标准.     

废水中GaAs、Ga~(3+)、Ge~(4+)对活性污泥脱氢酶的影响及其抑制动力学

以活性污泥脱氢酶的活性作为毒性指标,研究了半导体材料GaAs、Ga~(3+)、Ge~(4+)对活性污泥活性的抑制影响,并用Hg~(2+)作为参比材料;同时对抑制动力学也作了初步研究。实验表明,GaAs、Ga~(3+)、Ge~(4+)及Hg~(2+)的10％抑制浓度分别为45.00,371.63,0.13ppm/gMLSS,GaAs、Ga~(3+)、Ge~(4+)和Hg~(2+)在浓度分别为180,700,250和1.25ppm/g MLSS时的抑制常数分别为1.30×10~(-3),7.05×10~(-3),6.12×10~(-3)和5.49×10~(-3)mmol,且其抑制类型均属可逆非竞争性抑制。     

生物可降解螯合剂[S,S]-乙二胺二琥珀酸和乳酸乙酯提取土壤中重金属的研究

研究了生物可降解的有机螯合剂[S,S]-乙二胺二琥珀酸([S,S]-EDDS,简写为EDDS)和乳酸乙酯(EL)对重金属污染土壤中重金属的提取效率,并用X射线衍射(XRD)和红外光谱(FT-IR)分析了螯合剂提取对土壤理化性质的影响.结果表明:EDDS对土壤中的Cd、Cu、Pb和Zn有较高的提取率,效果比EL好;EDDS和EL混合提取的重金属提取率增加,但相比单独使用EDDS没有超过10%.FT-IR分析表明,提取前后FT-IR谱图中特征吸收频率没有显著改变,但强度有所改变.XRD分析表明,提取前后土壤晶格结构发生明显的变化,螯合剂提取改变了土壤微观结构.     

Effect of noise exposure (85 dB ) on testicular adrenocortical steroidogenic key enzymes, acid and alkaline phosphatase activities of sex organs in mature albino rats

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C/N比对嗜酸细菌X-29产氢能力及其酶活性的影响

C/N比影响细菌的物质和能量代谢,为了提高产氢细菌的产氢效能,通过间歇产氢实验和酶活性分析方法,分析了在不同C/N比下嗜酸产氢细菌X-29的产氢能力以及氢化酶和乙醇脱氢酶的活性表达情况.研究结果表明,C/N比对产氢细菌的代谢及其相关酶的表达有显著的影响.虽然在不同C/N比下单位生物量的液相末端发酵产物差异不大,但是产氢能力存在显著的差异,当C/N比为14时产氢细菌X-29具有最大累积产氢量2 210.9mL/g.在不同C/N比下氢化酶的表达活性不同,氢化酶活性随着发酵的进行达到高峰后迅速降低,氢化酶的表达周期较短.乙醇脱氢酶活性随着代谢进程逐渐升高后而趋于平稳,不同C/N比时表达活性差异较小,表达周期较长.在C/N比为14时,氢化酶和乙醇脱氢酶的活性最高,分别为2.8μmol·(min·mg)^-1和33.2μmol·(min·mg)^-1.     

投加氢氧化铁对SMBR中活性污泥性能的影响

试验研究了在SMBR中投加不同量氢氧化铁对出水水质以及膜污染的影响。结果表明,生物铁-SMBR中随氢氧化铁投加量的增加,COD出水及去除率略有提高;氢氧化铁投加量为5%时,对活性污泥的活性促进作用最强;活性污泥SVI的降低主要是氢氧化铁絮体本身的化学絮凝作用所致;试验条件下氢氧化铁最佳投加量为混合液污泥浓度的5%时,半透膜压增长最慢,膜污染程度最轻。     

我国14种典型土壤脲酶、脱氢酶活性对汞胁迫的响应

Hg作为环境的主要污染重金属之一,其对土壤酶的影响是表征其环境效应的重要方面,结果可为土壤环境监测等提供生物学依据.因此,本文通过室内模拟试验,较系统地分析了全国14种主要类型18个土样的脲酶和脱氢酶活性在Hg胁迫下的响应.结果表明,Hg会抑制土壤酶活性,其降幅随土壤类型的不同有明显差异;随着Hg含量的升高,土壤脲酶和脱氢酶活性均显著降低;模型U=A/(1+B×C)可较好地拟合酶活性(U)与汞含量(C)之间的关系,揭示出土壤脲酶和脱氢酶在一定程度上可监测土壤Hg污染的程度,且机理为完全抑制(包括竞争性抑制和非竞争性抑制)作用.同时,实验获得的供试土样脲酶的生态剂量(ED10)范围为0.08~0.77 mg·kg-1,脱氢酶ED10范围为0.11~2.58mg·kg-1,从土壤酶角度获得的土壤汞轻度污染临界值为0.08 mg·kg-1,此值要小于国家土壤质量标准中的二级标准.有机质、pH、CEC和粘粒显著影响了汞与土壤脱氢酶的关系,上述4个土壤性状参数值越高,汞对土壤酶的毒害作用就越弱;酸性土壤中汞的毒害作用强于碱性土壤.表明在我国主要土壤类型上,土壤脲酶、脱氢酶对Hg毒性均较为敏感,可在更广范围内作为Hg污染程度的监测指标之一.     

土壤微生物电化学系统降解四环素的机理

以四环素为研究对象,构建土壤微生物电化学系统(SMES),避光恒温培养58d后进行采样分析,研究了四环素降解、土壤理化性质、酶活性和三域微生物之间的内在联系,以揭示四环素在SMES中的生物降解机理.结果表明,采用SMES处理后,四环素降解率从52％显著提升至70％.与对照处理相比,脱氢酶活性在SMES中显著提升了144...     

Monitoring impact of mefenacet treatment on soil microbial communities by PCR-DGGE fingerprinting and conventional testing procedures

The effect of acetanilide herbicide mefenacet on soil microbial communities was studied using paddy soil samples with different short-term treatments. The culturable bacteria （plate counts）, dehydrogenase activity and changes in community structure （denaturing gradient gel electrophoresis （DGGE） analysis） were used for biological community assessments. Mefenacet was a significant stimulus to cultural aerobic bacteria and dehydrogenase activity while Sphingobacterium multivorum Y1, a bacterium efficiently degrading the mefenacet, only induced the increasing colony-forming unit （CFU） of bacteria but little effect on dehydrogenase activity during the whole experiment. The degree of similarity between the 16S rDNA profiles of the communities was quantified by numerically analyzing the DGGE band patterns. Similarity dendrograms showed that the microbial community structures of the mefenacet-treated and non-treated soils were not significantly different. But supplement of S. multivorum Y1 could increase the diversity of the microbial community in the mefenacet-polluted paddy soil. This work is a new attempt to apply the S. multivorum Y1 for remediation of the mefenacet-polluted environments.     

Prenatal diagnosis of pyruvate dehydrogenase E1α subunit deficiency

Pyruvate dehydrogenase (PDH) E1α subunit deficiency is an X-linked inborn error of metabolism affecting males and females with equal frequency. The diagnosis is usually based on determination of enzyme activity, although this may present difficulties in some females because of X-inactivation patterns favouring expression of the normal X chromosome. This is a particular problem for prenatal diagnosis using chorionic villus cells where normal enzyme assay results do not necessarily exclude the diagnosis and confirmatory X-inactivation analysis may be complicated by variable methylation of active and inactive X chromosomes. We describe prenatal diagnosis in two pregnancies in a family following diagnosis of a PDH E1α deficient male. The first prenatal diagnosis was performed by enzyme assay, but by the time of the subsequent pregnancy, the underlying mutation in the affected male had been identified and direct gene analysis was possible. This study highlights the limitations of diagnosis of PDH E1α deficiency based on measurement of the gene product and illustrates the need for mutation analysis in affected individuals.