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81.
The geochemical cycling of cobalt (Co) has often been considered to be controlled by the scavenging and oxidation of Co(II) on the surface of manganese [Mn(III,IV)] oxides or manganates. Because Mn(II) oxidation in the environment is often catalyzed by bacteria, we have investigated the ability of Mn(II)-oxidizing bacteria to bind and oxidize Co(II) in the absence of Mn(II) to determine whether some Mn(II)-oxidizing bacteria also oxidize Co(II) independently of Mn oxidation. We used the marine Bacillus sp. strain SG-1, which produces mature spores that oxidize Mn(II), apparently due to a protein in their spore coats (R.A. Rosson and K. H. Nealson, J. Bacteriol. 151:1027-1034, 1982; J. P. M. de Vrind et al., Appl. Environ. Microbiol. 52:1096-1100, 1986). A method to measure Co(II) oxidation using radioactive 57Co as a tracer and treatments with nonradioactive (cold) Co(II) and ascorbate to discriminate bound Co from oxidized Co was developed. SG-1 spores were found to oxidize Co(II) over a wide range of pH, temperature, and Co(II) concentration. Leucoberbelin blue, a reagent that reacts with Mn(III,IV) oxides forming a blue color, was found to also react with Co(III) oxides and was used to verify the presence of oxidized Co in the absence of added Mn(II). Co(II) oxidation occurred optimally around pH 8 and between 55 and 65°C. SG-1 spores oxidized Co(II) at all Co(II) concentrations tested from the trace levels found in seawater to 100 mM. Co(II) oxidation was found to follow Michaelis-Menten kinetics. An Eadie-Hofstee plot of the data suggests that SG-1 spores have two oxidation systems, a high-affinity-low-rate system (Km, 3.3 × 10-8 M; Vmax, 1.7 × 10-15 M · spore-1 · h-1) and a low-affinity-high-rate system (Km, 5.2 × 10-6 M; Vmax, 8.9 × 10-15 M · spore-1 · h-1). SG-1 spores did not oxidize Co(II) in the absence of oxygen, also indicating that oxidation was not due to abiological Co(II) oxidation on the surface of preformed Mn(III,IV) oxides. These results suggest that some microorganisms may directly oxidize Co(II) and such biological activities may exert some control on the behavior of Co in nature. SG-1 spores may also have useful applications in metal removal, recovery, and immobilization processes. 相似文献
82.
Continuous, real-time monitoring of the oxygen uptake rate (OUR) in animal cell bioreactors 总被引:1,自引:0,他引:1
A new method for real-time monitoring of the oxygen uptake rate (OUR) in bioreactors, based on dissolved oxygen (DO) measurement at two points, has been developed and tested extensively. The method has several distinct advantages over known techniques.It enables the continuous and undisturbed monitoring of OUR, which is conventionally impossible without gas analyzers. The technique does not require knowledge of k(L)a. It provides smooth, robust, and reliable signal. The monitoring scheme is applicable to both microbial and mammalian cell bioprocesses of laboratory or industrial scale. The method was successfully used in the cultivation of NSO-derived murine myeloma cell line producing monoclonal antibody. It was found that while the OUR increased with the cell density, the specific OUR decreased to approximately one-half at cell concentrations of 16 x 10(6) cells/mL, indicating gradual reduction of cell respiration activity. Apart from the laboratory scale cultivation, the method was applied to industrial scale perfusion culture, as well as to processes using other cell lines. (c) 1994 John Wiley & Sons, Inc. 相似文献
83.
Panose, a major component of isomalto-oligosaccharides, was selectively produced from maltose using transglucosylation reaction catalyzed by intact cells of Aureobasidium pullulans. When 50 %(w/v) maltose was used as a substrate, the maximum concentration of panose accumulated in the final reaction mixture was about 50 %(w/w) after 120 hr reaction at 55 °C. 相似文献
84.
Capsid assembly and involved function analysis of twelve core protein mutants of duck hepatitis B virus. 总被引:6,自引:6,他引:0
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The roles of different regions of the duck hepatitis B virus (DHBV) core protein on viral capsid assembly and related functions were examined. Twelve deletion and insertion mutations which covered 80% of the DHBV C open reading frame were constructed and expressed in Escherichia coli. The N-terminal region (amino acids 3 to 66) of DHBV core protein was important for its tertiary structure and function in E. coli. The expressed core mutants without this region apparently inhibited E. coli growth. The results of transmission electron microscopy of E. coli thin sections, capsid agarose gel, and sucrose gradient sedimentation demonstrated that a few DHBV core mutants with insertion in the N terminus and deletion in the C terminus retained the ability to form core-like particles in E. coli. However, other mutations in most of N-terminal and central regions strongly inhibited the self-assembly ability of DHBV core protein in E. coli. In addition, the mutant with a C-terminal region deletion (amino acids 181 to 228) lost most of the nucleic acid-binding activity of the DHBV core protein. 相似文献
85.
Chang-Zhi Dong Jean-Luc Montillet Christian Triantaphylidès 《Physiologia plantarum》1994,90(2):307-312
The effects of ionizing radiation, used in post-harvest treatment of fruit and vegetables. were investigated on cultured apple cells ( Pyrus malus L. cv. Royal Red) on a short-term period. Irradiation (2 kGy) induced an increase of passive ion effluxes from cells and a decrease of cell capacity to regulate external pH. These alterations are likely due to effects on plasma membrane structure and function and were further investigated by studying the effects of irradiation on plasma membrane H+ -ATPase activity. Plasma membrane-enriched vesicles were prepared and the H+ -ATPase activity was characterized. Irradiation of the vesicles induced a dose dependent inhibition of H+ -ATPase activity. The loss of enzyme activity was immediate, even at low doses (0.5 kGy), and was not reversed by the addition of 2m M dithiothreitol. This inhibition may be the result of an irreversible oxidation of enzyme sulfhydryl moieties and/or the result of changes induced within the lipid bilayer affecting the membrane-enzyme interactions. Further analysis of the H+ -ATPase activity was carried out on vesicles obtained from irradiated cells confirming the previous results. In vivo recovery of activity was not observed within 5 h following the treatment, thus explaining the decrease of cell capacity to regulate external pH.
This rapid irreversible inhibition of the plasma membrane H+ -ATPase must be considered as one of the most important primary biochemical events occurring in irradiated plant material. 相似文献
This rapid irreversible inhibition of the plasma membrane H
86.
植物细胞离析酶的制备和应用 总被引:2,自引:0,他引:2
用 Aspergillus sp.A-19菌经固体发酵研制成一种新的植物细胞离析酶(SeparatasezA—P)。其离析单细胞的酶活力平均为70 767u/g,有效作用的pH在3.0—7.0,温度为20—45℃。发酵培养基配方是麸皮:桔皮粉:(NH4)2SO4(w/w)为100:100:O.63,料水比为1 :2.0,培养适宜条件为25℃、60小时。 相似文献
87.
红毛五加叶的三萜皂甙 总被引:2,自引:0,他引:2
红毛五加(AcanthopanaxgiraldiiHarms)系五加科五加属植物,分布于河北、河南、四川、陕西、甘肃等省,有祛风湿、通关节、强筋骨、治痿痹等功效[1]。其化学成分未见报道。本文报道红毛五加叶的5个三萜皂甙(甙Ⅰ、Ⅱ、Ⅲ、Ⅳ和Ⅴ)的分离鉴定。它们均首次从该属植物发现,其结构如下: R1 R2 Ⅰ rham-(1→2)-ara H Ⅱ H rham-(1→4)-glc-(1→6)-glc … 相似文献
88.
河西走廊不同生态型芦苇核酸代谢季节动态研究 总被引:4,自引:0,他引:4
分布在甘肃河西走廊的4 种生态型芦苇(Phragm itescom m unisTrin.)的核酸代谢季节变化有差异。盐化草甸芦苇RNA 含量持续增加,DNA 含量相对稳定,其它3 种生态型芦苇的RNA 和DNA 含量以5月份为最高。过渡带芦苇的RNA 含量、沼泽芦苇及沙丘芦苇的DNA含量9 月份略有增高。盐化草甸芦苇与过渡带芦苇的DNase和RNase的活性7 月份最高,沼泽芦苇与沙丘芦苇的DNase和RNase活性5—9 月份呈增高趋势。盐化草甸芦苇的DNA 和RNA 合成活性不断升高,过渡带芦苇和沼泽芦苇的DNA 和RNA 合成活性及沙丘芦苇的RNA 合成活性5—9月份均降低,仅沙丘芦苇的DNA合成活性增强。RNA 聚丙烯酰胺梯度凝胶电泳分析结果表明,4 种生态型芦苇均含有25S、23S、18S、16S大分子量rRNA 和小分子量5.8S、5S、4.5SrRNA 及4StRNA。大分子量RNA 的含量高于小分子量RNA 含量。不同生态型及同一生态型芦苇的不同发育时期,相同的RNA 组分含量各不相同。且发育过程中23S、18S、16SrRNA 在不同月份发生不同程度的降解。由此,我们认为,核酸代谢的差异性是4 种生态型由生长转入衰 相似文献
89.
三褶脉紫菀中的新二萜甙 总被引:1,自引:0,他引:1
三褶脉紫菀(AsterageratoidesTurcz.)系菊科多年生草本植物,遍布全国,是民间常用的中药,有清热解毒、祛痰镇咳的功效[1,2]。化学工作者们曾从其同属植物紫菀(AstertararicusL.f.)中分离到紫菀酮(shionone)、槲皮素(quercetin)、无羁萜(friedelin)、表无羁萜(epifriedelinel)、毛叶醇(lachnophyllol)、乙酸毛叶酯(lachnophyllolacetate)、茴香醚(anethole)以及紫菀三萜皂甙[2—4]… 相似文献
90.
Jan Hendrickx Paul Coucke Marie-Claude Hors-Cayla G. Peter A. Smit Yoon S. Shin Johann Deutsch Jan Smeitink Ruud Berger Philip Lee John Fernandes Patrick J. Willems 《Genomics》1994,21(3)
We describe here a new type of X-linked liver glycogen storage disease. The main symptoms include liver enlargement and growth retardation. The clinical and biochemical abnormalities of this glycogenosis are similar to those of classical X-linked liver glycogenosis due to phosphorylase kinase deficiency (XLG). However, in contrast to patients with XLG, the patients described here have no reduced phosphorylase kinase activity in erythrocytes and leukocytes, and no enzyme deficiency could be found. Linkage analysis of four families with this X-linked type of liver glycogenosis assigned the disease gene to Xp22. Lod scores obtained with the markers DXS987, DXS207, and DXS999 were 3.97, 2.71, and 2.40, respectively, all at 0% recombination. Multipoint linkage analysis localized the disease gene between DXS143 and DXS989 with a maximum lod score of 4.70 at θ = 0, relative to DXS987. As both the classical XLG gene and the liver α-subunit of PHK (PHKA2) are also located in Xp22, this variant type of XLG may be allelic to classical XLG, and both diseases may be caused by mutations in PHKA2. Therefore, we propose to classify XLG as XLG type I (the classical type of XLG) and XLG type II (the variant type of XLG). 相似文献