Structural investigation of an arabinan from cabbage (Brassica oleracea var. capitata)

An arabinan has been isolated from the hot water-soluble pectic substances of cabbage cell wall material. Methylation analysis involving GC-MS of methylated alditol acetates formed from the methylated arabinan has shown that the parent polysaccharide is highly branched and of the same structural type as other arabinans associated with seed pectins.     

藻际环境中胞外聚合物的研究进展

微藻向细胞周围释放营养物质而形成了独特的藻际微环境,吸引了大量细菌的定殖。藻际环境中藻菌关系错综复杂,其间充斥着多样的物质交换与信息交流。以胞外聚合物(extracellularpolymeric substances,EPS)为代表的有机质在其中起着纽带作用。微藻和细菌都可以产生EPS,其过程受多种因素的调节。EPS在藻际环境中具有重要的生态功能,包括参与生物被膜(biofilm)的形成,影响藻菌共生关系的建立以及调节藻际微生物群落组成等。此外,EPS中的一大类别透明胞外聚合物颗粒(transparent exopolymer particles,TEP)还介导了海洋溶解有机碳向颗粒有机碳的转化,参与了海洋碳循环过程。本文以EPS的产生、组成以及对碳转化的影响为重点,综述了其在藻际生态位(Niche)中的生态功能,以期为深入理解藻际环境中的有机质特征和藻菌共生关系提供理论依据。     

The effect of sulfite on the yeast Saccharomyces cerevisiae

After a short period of tolerance, living cells of Saccharomyces cerevisiae were irreversibly damaged by low concentrations of sulfite. The length of the period of tolerance and the rate of the damaging effect depended on the concentration on sulfite, pH-value, temperature, the physiological state of the cells, and incubation time.Inhibitors of protein synthesis and mitochondrial ATP synthesis did not alter the deleterious effect of sulfite on living cells. Furthermore, cell damage leading to inhibition of colony formation occured under aerobic as well as under anaerobic conditions.Prior to cell inactivation sulfite induced the formation of respiratory deficient cells.The active agent was shown to be SO₂.     

Creatine prevents the imbalance of redox homeostasis caused by homocysteine in skeletal muscle of rats

Homocystinuria is a neurometabolic disease caused by severe deficiency of cystathionine beta-synthase activity, resulting in severe hyperhomocysteinemia. Affected patients present several symptoms including a variable degree of motor dysfunction, being that the pathomechanism is not fully understood. In the present study we investigated the effect of chronic hyperhomocysteinemia on some parameters of oxidative stress, namely 2′7′dichlorofluorescein (DCFH) oxidation, levels of thiobarbituric acid-reactive substances (TBARS), antioxidant enzyme activities (SOD, CAT and GPx), reduced glutathione (GSH), total sulfhydryl and carbonyl content, as well as nitrite levels in soleus skeletal muscle of young rats subjected to model of severe hyperhomocysteinemia. We also evaluated the effect of creatine on biochemical alterations elicited by hyperhomocysteinemia. Wistar rats received daily subcutaneous injection of homocysteine (0.3–0.6 μmol/g body weight), and/or creatine (50 mg/kg body weight) from their 6th to the 28th days age. Controls and treated rats were decapitated at 12 h after the last injection. Chronic homocysteine administration increased 2′7′dichlorofluorescein (DCFH) oxidation, an index of production of reactive species and TBARS levels, an index of lipoperoxidation. Antioxidant enzyme activities, such as SOD and CAT were also increased, but GPx activity was not altered. The content of GSH, sulfhydril and carbonyl were decreased, as well as levels of nitrite. Creatine concurrent administration prevented some homocysteine effects probably by its antioxidant properties. Our data suggest that the oxidative insult elicited by chronic hyperhomocystenemia may provide insights into the mechanisms by which homocysteine exerts its effects on skeletal muscle function. Creatine prevents some alterations caused by homocysteine.     

Patterns of oligosaccharide production by polygalacturonases

The products of hydrolytic action of 18 enzyme preparations at pH 3·5 and 5·5 on pectate were analyzed by gel-filtration chromatography early in the course of reaction (8–15% hydrolysis), and at a time 10 times that required for 10% hydrolysis. The degree of hydrolysis at the latter time varied from 25 to 74%. Three patterns of oligosaccharide production could be distinguished: endo-hydrolysis, exo-hydrolysis, and that due to S-polygalacturonase. The initial products of endo-hydrolysis were mixed oligosaccharides 5–30 units long; monomer and dimer appeared early but represented less than 2% of the products until late in the reaction. exo-Polygalacturonase (not entirely free of endo-) showed predominant production of the monomer and was clearly evident when mixed with four parts of endo-polygalacturonase. The time course of reducing group production by highly purified S-polygalacturonase could be reproduced by the above mixture of exo- and endo-polygalacturonases, but the pattern of products and the pH relations could not. The initial products of S-polygalacturonase were monomer, dimer and pentamer with lesser amounts of trimer and tetramer. After the hydolysis of the polymer and large oligomers, the pentamer was attacked by S-polygalacturonase, in the same way that the accumulated hexamer, etc. were finally hydrolysed by the endo-polygalacturonase.     

外源5-氨基乙酰丙酸对NaCl胁迫下黑果枸杞幼苗生理及生长的影响

5-氨基乙酰丙酸(ALA)是植物血红素、叶绿素等四吡咯化合物的关键生物合成前体,对植物适应非生物胁迫至关重要。为验证外源ALA对黑果枸杞幼苗生理生长的影响,该研究用300 mmol·L^-1 NaCl和不同浓度(0、5、10、15、20、25 mg·L^-1)的ALA共同处理黑果枸杞幼苗,并测定其相关的生理指标和生长指标,综合评价各处理幼苗的耐盐性。结果表明：(1)NaCl胁迫使黑果枸杞幼苗总生物量和叶片总叶绿素、类胡萝卜素、可溶性糖含量以及过氧化物酶(POD)活性较CK分别显著降低了33.39%、19.06%、24.38%、39.57%和47.91%(P<0.05),使黑果枸杞幼苗脯氨酸和丙二醛的含量较CK分别显著增加了165.74%和49.16%。(2)当外源ALA和NaCl同时处理时,黑果枸杞幼苗叶片类胡萝卜素和丙二醛含量、POD和过氧化氢酶(CAT)活性以及株高、总生物量均恢复至对照水平,叶片总叶绿素和脯氨酸含量以及SOD活性较CK显著增加。(3)黑果枸杞幼苗叶片叶绿素和脯氨酸含量以及抗氧化酶活性、生物量等指标随ALA浓度增加均呈先...     

Fullerol-fluorescein isothiocyanate phosphorescent labeling reagent for the determination of glucose and alkaline phosphatase

The active -OH group in fullerol (F-ol) could react with the dissociated -COOH group in fluorescein isothiocyanate (FITC) to form F-ol-(FITC)_n, which could emit room temperature phosphorescence (RTP) signal of F-ol and FITC on acetate cellulose membrane (ACM), respectively. Their RTP signals were enhanced by N,N-dimethylaniline (DMA). The labeling reaction between the -NCS group of FITC in DMA-F-ol-(FITC)_n and the -NH₂ group in wheat germ agglutinin (WGA) produced DMA-F-ol-(FITC)_n-WGA, which could further take affinity adsorption (AA) reaction with bioactive substances (BS), such as glucose and alkaline phosphatase (AP), to produce DMA-F-ol-(FITC)_n-WGA-BS. Both of these two products could maintain the good RTP characteristics of F-ol and FITC. Based on the facts above, a new phosphorescent labeling reagent, DMA-F-ol-FITC, was developed, and a new affinity adsorption solid substrate room temperature phosphorimetry (AASSRTP) for the determination of BS was established. This method was applied to the determination of BS in human serum and the diagnosis of diseases, with the results agreeing very well with those of enzyme-linked immunosorbent assay (ELISA). The mechanism of DMA-F-ol-(FITC)_n labeling of WGA and AASSRTP for the determination of BS is discussed.     

Laboratory Hints from the Literature

Chaze, J. Sur le mode de formation et la detection des alcaloides dans la plantule de tabac. Bull. d'Histol. Appl., 5, 253. 1928.

Nan, Yao. Sur un fixateur cytologique particulièrement adapté aux tissues des insectes. Bull. d'Histol. Appl., 4, 71, 1927.

Reichardt, H., and Wetzel, A. Paraffineinbettungsmethode nach vorhergegangener Zelloidindurchtränkung unter Vermeidung der härtenden Intermedien, Xylol, Benzol, Chloroform. Zeit. f. wiss. Mikr., 45, 476-479. 1928.

Erb, N. M. A rapid stain for direct miroscopic examination of milk. J. Lab. & Clin. Med., 14, 377. 1929.

Galesesco, P., and Bratiano, S. Coloration des graisses par l'extrait alcoolique de Daucus carota. Compt. Rend. Soc. Biol., 99, 1460. 1928.

Goldner, J' Résultats obtenus chez la seiche par l'emploi de divers colorants vitaux Comp. Rend. Soc. Biol., 99, 1323. 1928.

Hadjioloff, A. Une modification rapide de la méthode de Weigert-Pal. Bull. d'Histol. Appl., 5, 431-434. 1928.

Hausdorf, G. Farbung zur Darstellung reifer Samenzellen im Hodenschnittpraparat. Zeit. f. wiss. Mikr., 44, 327-328. 1927.

Houcke, E. Emploi des colorants mixtes en technique histologique. Comp. Rend. Soc. Biol., 99, 783. 1928.

Houcke, E. Emploi des mélanges de fuchsines et de blues basiques pour la coloration histologique. Comp. Rend. Soc. Biol., 99, 786. 1928.

Houcke, E. Emploi du mélange rhodamine-blue de méthylène dans la coloration des tissus splénique et lymphcïde. Comp. Rend. Soc. Biol., 99, 788. 1928.

Lillie, R. D. Erne Schnellmethode zur Toluidinblau-Schleimfarbung. Zeit. f. wiss. Mikr., 45, 381. 1928.

Ochs, Georg Wilhelm. Über den Einfluss der Temperatur auf die Färbung von Blutausstrich-Präparaten. Folia Hematologica, 37, 241-257. 1928.

Verne, Jean. Une nouvelle coloration élective de la myeline. Bull. d'Histol. Appl., 5, 223-224. 1928.     

Potential role of bacterial extracellular polymeric substances as biosorbent material for arsenic bioremediation

Carcinogenic effects of arsenic through consumption of contaminated water are an alarming threat and there is an emergent need to reduce extremely high levels of toxic arsenic from environment. Bacterial biofilms produce polyanionic extracellular polymeric substance (EPS) that is considered an excellent biosorbent material for the remediation of toxic metals and metalloids. This study was aimed to investigate the role of bacterial EPS in arsenic bioremediation. EPS was extracted from biofilm forming and arsenic reducer bacterial strains that were isolated from industrial waste water and characterized biochemically. Fourier transform infrared spectroscopy was also performed to study functional groups. Both Exiguobacterium profundum PT2 and Ochrobactrum ciceri SW1 exhibited enhanced EPS production in the presence of arsenic. Arsenic stress increased protein and carbohydrate contents in the EPS of both bacterial strains as indicated by the peaks of 1363 to 1613 and 1035 to 1218?cm^?1 wavenumbers, respectively to cope with arsenic present in the surroundings. Shifting of peaks in As⁵⁺ treated samples from 1363 to 1379, 847 to 800 and 1211 to 1134?cm^?1 demonstrated the involvement of proteins, carbohydrates and phosphates in the sequestration of arsenic. Scanning electron microscopic examination of EPS revealed structural alterations such as the presence of closely embedded large clumps with interstitial spaces between stacked layers of the EPS of E. profundum PT2 treated with As⁵⁺ displayed the enhanced polysaccharide content and arsenic sorption. Therefore, increased production of bacterial EPS with large number of polyanionic functional groups on its surface having tendency to sequester arsenic through electrostatic or covalent interactions presented EPS an excellent biosorbent material for arsenic bioremediation.