工厂化生产海鲜菇菌包污染霉菌的鉴定及防治

对工厂化生产中海鲜菇菌包污染霉菌进行分离,根据霉菌的形态特征、培养性状及ITS序列分析,鉴定其为哈茨木霉、拟康氏木霉、脉孢霉、长枝木霉、黑曲霉、产红青霉和产黄青霉;在此基础上探讨了常用抑菌剂对霉菌的防治效果及对海鲜菇菌丝生长的影响。结果表明,质量浓度100 mg/L克霉灵对哈茨木霉、黑曲霉、产红青霉、产黄青霉、拟康氏木霉有强抑制作用,质量浓度100 mg/L多菌灵对长枝木霉、产红青霉、产黄青霉、拟康氏木霉有强抑制作用,二者对海鲜菇菌丝生长的抑制都比较弱。可为海鲜菇工厂化生产中污染霉菌的综合防治提供参考。     

里氏木霉与黑曲霉混合发酵产纤维素酶及其水解特性

研究了利用里氏木霉和黑曲霉混合培养产纤维素酶,以黑曲霉孢子悬浮液的不同活化浓度及不同的活化时间来寻找2个菌种发挥最大协同作用的结合点以及所产纤维素酶的水解特性。以里氏木霉单一培养和黑曲霉单一培养为参照进行对比研究。底物为农林废弃物之一的玉米秸秆,经过蒸气爆破预处理后,用作产酶C源。结果表明:黑曲霉孢子悬浮液活化浓度为10个/mL,活化时间为12 h时,滤纸酶比酶活最高,达3.32 U/mL,高于里氏木霉单一培养的2.25 U/mL,β-葡萄糖苷酶比酶活达1.32 U/mL,高于里氏木霉单一培养的0.57 U/mL。为进一步验证混合菌产纤维素酶的水解效果,利用混合菌产纤维酶的酶液及里氏木霉产纤维素酶的酶液进行酶水解实验,当酶用量为20 U/g绝干纤维素,底物质量浓度为100 g/L条件下水解48 h,混合菌所产酶液酶解得率达70.00%,高于里氏木霉所产酶液的酶解得率63.05%。实验表明里氏木霉与黑曲霉混合培养产酶是可行的,并优于单一菌种培养。     

泡桐花体外抑菌作用及黄酮含量的测定

本文首次采用滤纸片法对泡桐花提取液的不同萃取部分进行了体外抑菌试验并用紫外分光光度法对泡桐花的花冠和花萼中总黄酮含量进行了测定。结果表明不同萃取部分对金黄色葡萄球菌,大肠杆菌,枯草芽孢杆菌均有不同程度的抑制作用,其中对金黄色葡萄球菌作用最强,而对黑曲霉,啤酒酵母,产黄青霉无明显抑制作用。含量测定表明花萼中黄酮含量明显高于花冠。     

五种芳香类挥发物质对酪蝇的引诱效果

室内采用Y-型嗅觉仪测定不同浓度(1.0×10-6,1.0×10-5,1.0×10-4和1.0×10-3mL/mL)水杨醛、水杨酸甲酯、苯乙醛、苯甲醛、桂醇5种化合物对酪蝇Piophila casei(L.)成虫的引诱效果。结果表明:1.0×10-6和1.0×10-5mL/mL苯乙醛,1.0×10-6mL/mL苯甲醛,1.0×10-5和1.0×10-4mL/mL水杨醛均对雌、雄虫表现明显的引诱效果。1.0×10-3mL/mL苯乙醛、水杨醛和苯甲醛对酪蝇雌、雄虫具有明显的驱避效果。桂醇和水杨酸甲酯在所测试的浓度范围内对雄虫具有明显的驱避效果。水杨酸甲酯在浓度为1.0×10-6mL/mL对雌虫有明显的引诱效果,其它浓度均对雌虫有明显的驱避效果。桂醇对雌虫有明显的驱避效果。这表明在高浓度时芳香物质对酪蝇成虫有驱避效果,在低浓度时对酪蝇成虫有引诱效果。     

茅苍术挥发油对三种内生真菌及七种外源真菌的抑菌活性

为了研究宿主植物次级代谢产物对内生真菌生长的抑制作用,以药用植物茅苍术及其内生真菌为材料,采用有机溶剂萃取法提取茅苍术挥发油,应用滤纸片扩散法和平板涂布法研究茅苍术挥发油对茅苍术内生真菌及其他外源真菌的抑菌作用.结果表明: 挥发油对3种内生真菌生长具有抑制作用;对酵母、水霉有很强的抑菌活性;对根霉、犁头霉抑菌作用不明显;对绿色木霉、黑曲霉的产孢具有抑制作用;对疫霉生长无抑制作用.在高浓度挥发油胁迫下,内生真菌菌丝分支增多,分支间距离变短,气生菌丝生长受到抑制.两种内生真菌对挥发油具有代谢转化能力,降低了其主要成分的含量.表明茅苍术挥发油对内生真菌生长具有限制作用,但内生真菌能够通过自身分解代谢适应茅苍术挥发油.     

紫穗槐种子提取物的抑菌活性研究

目的研究紫穗槐种子提取物的抑菌活性。方法将紫穗槐种子乙醇提取物分别通过石油醚、乙酸乙酯和正丁醇萃取,选择金黄色葡萄球菌和肺炎克雷伯杆菌为供试菌,采用试管二倍稀释法测定紫穗槐种子提取物的最小抑菌浓度（MIC）和最小杀菌浓度（MBC）,涂布平板法绘制杀菌曲线,电镜下观察药物对细菌超微结构的影响。结果紫穗槐种子提取物经乙酸乙酯萃取后对供试菌抑制作用较强,其中对金黄色葡萄球菌的MIC和MBC分别为2．5、5．0mg／mL;对肺炎克雷伯杆菌的MIC和MBC分别为5．0、10．0mg／mL;杀菌曲线结果表明,药物对供试菌的抑制作用存在浓度和时间依赖性;电镜结果说明,药物的作用可能与破坏菌体细胞壁、改变细胞膜通透性有关。结论紫穗槐种子提取物具有显著的抗菌活性。     

多棘海盘车皂甙抗菌活性研究

采用有机溶剂法从多棘海盘车中提取皂甙化合物,通过中性氧化铝柱的色素吸附以及AmberLite XAD-2树脂柱的富集,得到海星皂甙。采用“管碟法”分别研究了海星皂甙对4种细菌和4种真菌的体外抑菌作用。对细菌的抗菌效果表明：海星皂甙对金黄色葡萄球菌、腊样芽孢杆菌的生长有较好的抑制作用,最低抑菌浓度分别是10、12．5mg／mL,而对大肠杆菌则无抑菌作用;对真菌的抗菌效果表明：海星皂甙对黑曲霉的生长有显著的抑制作用,而对啤酒酵母、青霉、根霉则无抑菌作用。从而说明海星皂甙对细菌和真菌的抑制作用均有一定的选择性。     

产气气杆菌茁霉多糖酶的研究II．化学试剂对酶活力的影响

研究了某些化学试剂对产气气杆菌 Aerobacter aerogenes 的茁霉多糖酶 (Pullulanase EC3.2.1.41)活力的影响。Hg2+,Cu2+,Al3+,Fe3+等金属离子对酶活力有强烈的抑制作用,Ca2+,Mg2+有激活作用。1×10-3M的β-环状糊精完全抑制酶的活力,是竞争性抑制剂,其抑制常数Ki为0．55×10-5M。8M尿素,1.0M的盐酸胍,0.5％的SDS等蛋白质变性剂导致酶活力的完全丧失,在反应体系中有5×10-4M的Ca2+时,对酶有明显的保护作用。色氨酸残基的专一性修饰剂N-溴代琥珀酰亚胺(简称NBS)在1×10-4M的浓度下使酶活力完全丧失,甚至在1×10-5M的浓度下,只保留9％的活力,酶液在用NBS处理前加入不同浓度的底物,对活力有明显的保护作用,表明色氨酸残基对于茁霉多糖酶的活力是十分重要的。     

离子注入哈茨木霉筛选高产促植物生长物质菌株的研究

用 N+注入哈茨木霉所获得的突变型的发酵液浇灌水稻种子 ,结果发现 :5× 10 - 6、5× 10 - 5、2× 10 - 4木霉突变株发酵稀释液处理的种子幼苗长势优于对照组和木霉原种组。其 5 0倍、15 0倍木霉发酵稀释液浇灌的种子幼苗过氧化物酶同工酶与对照和原种相比均出现了新的谱带 A- 3、C- 3带。各突变株 5 0倍发酵稀释液和原种发酵液浇灌的水稻幼苗过氧化物酶同工酶出现了 B- 3带。而四种浓度的木霉发酵稀释液处理的水稻幼苗 ,其酯酶同工酶与对照组和原种组相比 ,无明显差异     

缬草与蜘蛛香挥发油的抗菌抗氧化活性研究

通过对缬草和蜘蛛香挥发油抗菌抗氧化活性的研究,为开发天然高效的抗菌抗氧化药物提供新的选择。采用纸片扩散法和试管稀释法对缬草和蜘蛛香挥发油进行抑菌圈大小及最小抑菌浓度的测定;用DPPH法对其抗氧化能力进行研究。结果表明:缬草和蜘蛛香挥发油均具有一定的抗菌作用,细菌试验中对金黄色葡萄球菌的作用最强,二者对其最小抑菌浓度分别为3.125 mg/mL和6.25 mg/mL;对真菌的抑制作用相对较弱,其中蜘蛛香挥发油作用强于缬草挥发油。两者挥发油不同浓度对DPPH自由基有较好的清除能力,实验浓度范围内,最高清除率分别达65.35%和71.75%,均强于阳性对照品BHT。     

Physicochemical and biological properties of 6(1),6(3),6(5)-tri-O-alpha-maltosyl-cyclomaltoheptaose (6(1),6(3),6(5)-tri-O-alpha-maltosyl-beta-cyclodextrin)

A unique multibranched cyclomaltooligosaccharide (cyclodextrin, CD) of 6(1),6(3),6(5)-tri-O-alpha-maltosyl-cyclomaltoheptaose [6(1),6(3),6(5)-tri-O-alpha-maltosyl-beta-cyclodextrin, (G(2))(3)-betaCD] was prepared. The physicochemical and biological properties of (G(2))(3)-betaCD were determined together with those of monobranched CDs (6-O-alpha-D-glucopyranosyl-alpha-cyclodextrin (G(1)-alphaCD), 6-O-alpha-D-glucopyranosyl-beta-cyclodextrin (G(1)-betaCD), and 6-O-alpha-maltosyl-beta-cyclodextrin (G(2)-betaCD)). NMR spectra of (G(2))(3)-betaCD were measured using various 2D NMR techniques. The solubility of (G(2))(3)-betaCD in water and MeOH-water solutions was extremely high in comparison with nonbranched betaCD and was about the same as that of the other monobranched betaCDs. The formation of an inclusion complex of (G(2))(3)-betaCD with stereoisomers (estradiol, retinoic acid, quinine, citral, and glycyrrhetinic acid) depends on the cis-trans isomers of guest compounds. The cis isomers of estradiol, retinoic acid, and glycyrrhetinic acid were included more than their trans isomers, while the trans isomers of citral and quinine fit more tightly than their cis isomers. (G(2))(3)-betaCD was the most effective host compound in the cis-trans resolution of glycyrrhetinic acid. Among the branched betaCDs, (G(2))(3)-betaCD exhibited the weakest hemolytic activity in human erythrocytes and showed negligible cytotoxicity in Caco-2 cells up to 200 microM. These results indicate unique characteristics of (G(2))(3)-betaCD in some biological responses of cultured cells.     

Spectral and thermodynamic properties of Ag(I), Au(III), Cd(II), Co(II), Fe(III), Hg(II), Mn(II), Ni(II), Pb(II), U(IV), and Zn(II) binding by methanobactin from Methylosinus trichosporium OB3b

Methanobactin (mb) is a novel chromopeptide that appears to function as the extracellular component of a copper acquisition system in methanotrophic bacteria. To examine this potential physiological role, and to distinguish it from iron binding siderophores, the spectral (UV–visible absorption, circular dichroism, fluorescence, and X-ray photoelectron) and thermodynamic properties of metal binding by mb were examined. In the absence of Cu(II) or Cu(I), mb will bind Ag(I), Au(III), Co(II), Cd(II), Fe(III), Hg(II), Mn(II), Ni(II), Pb(II), U(VI), or Zn(II), but not Ba(II), Ca(II), La(II), Mg(II), and Sr(II). The results suggest metals such as Ag(I), Au(III), Hg(II), Pb(II) and possibly U(VI) are bound by a mechanism similar to Cu, whereas the coordination of Co(II), Cd(II), Fe(III), Mn(II), Ni(II) and Zn(II) by mb differs from Cu(II). Consistent with its role as a copper-binding compound or chalkophore, the binding constants of all the metals examined were less than those observed with Cu(II) and copper displaced other metals except Ag(I) and Au(III) bound to mb. However, the binding of different metals by mb suggests that methanotrophic activity also may play a role in either the solubilization or immobilization of many metals in situ.     

Synthesis and luminescence properties of a blue-emitting Sr(3.5) Y(6.5) O(2) (PO(4) )(1.5) (SiO(4) )(4.5) :Eu(2+) phosphor

A novel blue‐emitting Sr_3.5Y_6.5O₂(PO₄)_1.5(SiO₄)_4.5:Eu²⁺ phosphor was synthesized via a solid‐state reaction. Powder X‐ray diffraction (XRD) analysis demonstrated that the Sr_3.5Y_6.5O₂(PO₄)_1.5(SiO₄)_4.5 host had a hexagonal crystal structure in the space group P6₃/m and unit cell parameters a = 9.418 Å, c = 6.900 Å. The as‐prepared phosphor showed a blue emission and all the main emission peaks were located at around 466 nm for different excitation wavelengths of 297, 333 and 391 nm. The temperature dependence of the photoluminescence property was investigated in the range 20–250 °C, and the emission intensity decreased to 71% of the initial value at room temperature on increasing the temperature to 150 °C. According to the classical theory of fluorescent thermal quenching, the activation energy (ΔE) for the thermal quenching luminescence of the as‐prepared Sr_3.45Y_6.5O₂(PO₄)_1.5(SiO₄)_4.5:0.05Eu²⁺ phosphor was determined to be 0.20 eV. Copyright © 2011 John Wiley & Sons, Ltd.     

Circular dichroism spectra of DNA quadruplexes [d(G(5)T(5))](4) as formed with G(4) and T(4) tetrads and [d(G(5)T(5)). d(A(5)C(5))]2 as formed with Watson-Crick-like (G-C)(2) and (T-A)(2) tetrads

We utilize electrophoresis and find that a thermally treated equimolar mixture of the oligonucleotide d(G(5)T(5)) and its complementary oligonucleotide d(A(5)C(5)) exhibits either two bands or a single band in one lane, depending on the conditions of the incubation solutions. The thermally treated d(G(5)T(5)) solution loaded in a different lane exhibits a single band of the parallel quadruplex [d(G(5)T(5))](4), which is composed of homocyclic hydrogen-bonded G(4) and T(4) tetrads previously proposed. For the thermally treated equimolar mixture of d(G(5)T(5)) and d(A(5)C(5)), the fast band is assigned to a Watson-Crick d(G(5)T(5)). d(A(5)C(5)) duplex, so that the slow band with the same low mobility as that of [d(G(5)T(5))](4) may be assigned to either [d(G(5)T(5))](4) itself or a [d(G(5)T(5)). d(A(5)C(5))](2) quadruplex. If the latter compound is true, this may be the antiparallel quadruplex composed of the heterocyclic hydrogen-bonded G-C-G-C and T-A-T-A tetrads proposed previously. After removing these three bands for the duplex and two kinds of hypothetical quadruplexes, we electrophoretically elute the corresponding compounds in the same electrophoresis buffer using an electroeluter. The eluted compounds are ascertained to be stable by electrophoresis. The circular dichroism (CD) and UV absorption spectra measured for the three isolated compounds are found to be clearly different. For the electrophoretic elution of the hypothetical [d(G(5)T(5))](4) quadruplex, the result of the molecularity of n = 4 obtained from the CD melting curve analysis provides further support for the formation of the parallel [d(G(5)T(5))](4) quadruplex already proposed. For the thermally treated equimolar mixture of d(G(5)T(5)) and d(C(5)A(5)), the fast band with a molecularity of n = 2 corresponds to the Watson-Crick duplex, d(G(5)T(5)). d(A(5)C(5)). The slow band with a molecularity of n = 4 indicates the antiparallel quadruplex [d(G(5)T(5)). d(A(5)C(5))](2), whose observed CD and UV spectra are different from those of [d(G(5)T(5))](4). By electrophoresis, after reannealing the eluted compound [d(G(5)T(5)). d(A(5)C(5))](2), a distinct photograph showing the band splitting of this quadruplex band into the lower duplex and upper quadruplex bands is not possible; but by a transilluminator, we occasionally observe this band splitting with the naked eye. The linear response polarizability tensor calculations for the thus determined structures of the [d(G(5)T(5))](4) quadruplex, the McGavin-like [d(G(5)T(5)). d(A(5)C(5))](2) quadruplex, and the Watson-Crick d(G(5)T(5)). d(A(5)C(5)) duplex are found to qualitatively predict the observed CD and UV spectra.     

New complexes of La(III), Ce(III), Pr(III), Nd(III), Sm(III), Eu(III) and Gd(III) ions with morin

New solid complex compounds of La(III), Ce(III), Pr(III), Nd(III), Sm(III), Eu(III) and Gd(III) ions with morin were synthesized. The molecular formula of the complexes is Ln(C₁₅H₉O₇)₃ · nH₂O, where Ln is the cation of lanthanide and n = 6 for La(III), Sm(III), Gd(III) or n = 8 for Ce(III), Pr(III), Nd(III) and Eu(III). Thermogravimetric studies and the values of dehydration enthalpy indicate that water occurring in the compounds is not present in the inner coordination sphere of the complex. The structure of the complexes was determined on the basis of UV-visible, IR, MS, ¹H NMR and ¹³C NMR analyses. It was found that in binding the lanthanide ions the following groups of morin take part: 3OH and 4CO in the case of complexes of La, Pr, Nd, Sm and Eu, or 5OH and 4CO in the case of complexes of Ce and Gd. The complexes are five- and six-membered chelate compounds.     

Spectral and thermodynamic properties of Ag(I), Au(III), Cd(II), Co(II), Fe(III), Hg(II), Mn(II), Ni(II), Pb(II), U(IV), and Zn(II) binding by methanobactin from Methylosinus trichosporium OB3b

Methanobactin (mb) is a novel chromopeptide that appears to function as the extracellular component of a copper acquisition system in methanotrophic bacteria. To examine this potential physiological role, and to distinguish it from iron binding siderophores, the spectral (UV–visible absorption, circular dichroism, fluorescence, and X-ray photoelectron) and thermodynamic properties of metal binding by mb were examined. In the absence of Cu(II) or Cu(I), mb will bind Ag(I), Au(III), Co(II), Cd(II), Fe(III), Hg(II), Mn(II), Ni(II), Pb(II), U(VI), or Zn(II), but not Ba(II), Ca(II), La(II), Mg(II), and Sr(II). The results suggest metals such as Ag(I), Au(III), Hg(II), Pb(II) and possibly U(VI) are bound by a mechanism similar to Cu, whereas the coordination of Co(II), Cd(II), Fe(III), Mn(II), Ni(II) and Zn(II) by mb differs from Cu(II). Consistent with its role as a copper-binding compound or chalkophore, the binding constants of all the metals examined were less than those observed with Cu(II) and copper displaced other metals except Ag(I) and Au(III) bound to mb. However, the binding of different metals by mb suggests that methanotrophic activity also may play a role in either the solubilization or immobilization of many metals in situ.     

Spectroscopic investigations of Er(3+) :CdO-Bi(2) O(3) -B(2) O(3) glasses

This article reports on the optical properties of Er³⁺ ions doped CdO–Bi₂O₃–B₂O₃ (CdBiB) glasses. The materials were characterized by optical absorption and emission spectra. By using Judd–Ofelt theory, the intensity parameters Ω_λ (λ = 2, 4, 6) and also oscillatory strengths were calculated from the absorption spectra. The results were used to compute the radiative properties of Er³⁺:CdBiB glasses. The concentration quenching and energy transfer from Yb³⁺–Er³⁺ were explained. The stimulated emission cross‐section, full width at half maximum (FWHM) and FWHM × values are also calculated for all the Er³⁺:CdBiB glasses. Copyright © 2011 John Wiley & Sons, Ltd.