DERMATITIS-PRODUCING ALGA LYNGBY A MAJUSCULA GOMONT IN HAWAII. II. BIOLOGICAL PROPERTIES OF THE TOXIC FACTOR1,2

The course of the reaction produced by intracutaneous injection of the toxin of Lyngbya majuscula Gomont is that of a severe acute inflammatory reaction. No protective or sensitizing effect is induced by a previous exposure. The response from intravenous injection into a rat indicates that the toxin acts as a general cell toxin. The protozoan Tetrahymena pyriformis and rabbit erythrocytes are lysed by the toxic principle, which also possesses antibacterial activity. Of the organisms tested, Mycobacterium species are markedly inhibited, while Bacillus cereus, Gaffkya tetragena, and Sarcina lutea are slightly to moderately inhibited. Other components of the alga, which are steam distillable, have been found to have antibacterial activity but are not involved in the skin reaction.     

略大凹顶藻化学成分的研究

对采自中国南海西沙群岛海域的略大凹顶藻（Laurencia majuscula)化学成分进行了研究,分离出了8个化合物,其中化合物1和2为首次报道的新化合物,经光谱分析,确证1为8－溴－1－烯－Chamigrene,2为谷甾－4,25－二烯－3β,6β－二醇。     

BIOSYNTHESIS OF THYROTROPIN RELEASING FACTOR BY NEWT (TRITURUS VIRIDESCENS) BRAIN IN VITRO. ISOLATION AND CHARACTERIZATION OF THYROTROPIN RELEASING FACTOR

Abstract— The in vitro biosynthesis of thyrotropin releasing factor (TRF) by hypothalamic and forebrain fragments from adult newts ( Triturus viridescens ) was studied by incubating the fragments in the presence of the radioactive amino acid precursors of thyrotropin releasing factor (TRF). The synthesized product was identified by successive chromatography and electrophoresis. A purification scheme was developed which can be applied to the processing of multiple samples labelled with l -[³H]proline and yields a TRF peak which, when derivatized with 1-fluoro-2,4-dinitrobenzene and applied to electrophoresis in acid buffer, yields a single radioactive peak corresponding to the migration of the N^im-Dnp derivative made from standard synthetic [³H]TRF. Both forebrain and hypothalamic fragments of the adult newt are capable of synthesizing a product which migrates with standard TRF after application of this purification scheme. Hypothalamic and forebrain fragments were also assayed for biological activity of TRF and it was determined that one newt hypothalamus contains approximately 200 pg TRF and that an equal amount of TRF is present in a forebrain piece of comparable size. It is concluded that newt TRF is identical to mammalian TRF (pGlu-His-Pro-NH₂) and that the storage and synthesis of this substance is not confined to the hypothalamus in this species.     

GLIDING MOTILITY OF OSCILLATORIA: ULTRASTRUCTURAL AND CHEMICAL CHARACTERIZATION OF THE FIBRILLAR LAYER1,2

Ultrastructural examination of platinum-carbon replicated trichomes or wall fragments of 3 Oscilatoria species readily displayed the fibrillar components of the presumed motility system. These fibrils had a lateral organization as well as longitudinal continuity and wavelike distortions, which are consistent with the hypothesized movement mechanism. The fibrils were sensitive to proteolytic enzymes but resistant to hydrolytic agents, suggesting a protein composition. The fibrils and motility were unaffected by cytochalasin B.     

ISOLATION AND CHARACTERIZATION OF GLYCOSAMINOGLYCANS IN BRAIN OF DIFFERENT SPECIES

Abstract— The uronic acid-containing glycosaminoglycans present in the brains of rat, monkey, chicken, sheep and rabbit were isolated into various fractions by combining the cetyl pyridinium procedure and DEAE-Sephadex column chromatography. The analyses of the fractions show that hyaluronic acid, chondroitin-4-sulphate, chondroitin-6-sulphate, heparan sulphate and a testicular hyaluronidase-resistant galactosamine-containing GAG are present in the brain of all the species studied. Hyaluronic acid is the major GAG (33–41 per cent). Chondroitin-4-sulphate (19–35 per cent), and heparan sulphate (11–19 per cent), are the next prominent GAGs, in all the species except chicken. The results indicate the similarity in the pattern of GAGs in the brain of all the species.     

ISOLATION AND CHARACTERIZATION OF THE SARCOPLASMIC RETICULUM OF SKELETAL MUSCLE

The sarcoplasmic reticulum (SR) of rabbit skeletal muscle was studied after isolation of a vesicle fraction and of vesicular subfractions by means of differential and density gradient centrifugations. The different fractions were examined electron microscopically by negative and positive staining; their content in protein and phospholipid and their ability to bind Ca⁺⁺ were determined. After homogenization, differential centrifugation yielded a "sarcovesicular fraction" (SVF) which was mainly composed of numerous vesicles of different types mixed with fibrous proteins and mitochondrial fragments. This SVF contained 2% of the protein and 25% of the phospholipid of the initial tissue extract. It had a high Ca⁺⁺ binding activity that was preserved for several days by storage in the presence of oxalate. After centrifugations of the SVF on sucrose density gradients, two vesicular subfractions were obtained which were characterized by different sedimentation rates, isopycnic banding, morphology, and composition in protein and phospholipid. (a) The low-density subfraction (ρ 1.10–1.12) contained a heterogeneous population of membranous structures: thick- and thin-walled vesicles, tubular formations, triads, and plasma membranes. Its content in protein and phospholipid was very low. (b) The high-density subfraction (ρ 1.13–1.17) was a very pure subfraction composed only of thin-walled vesicles. Its content in phospholipid was high and the ratio of phospholipid-phosphorus to protein was about 20. The calcium-binding activity found in the total SVF was recovered only in this latter homogeneous subfraction. The origin of these two subfractions from the SR is discussed.     

THE ULTRASTRUCTURE OF MITOSIS IN THE MARINE RED ALGA MEMBRANOPTERA PLATYPHYLLA1,2

Gametophyte germlings from unialgal cultures of Membranoptera platyphylla were examined with the electron microscope. The events of mitosis were observed in dividing cells near the thallus apex. In prophase the nucleus is spindle-shaped and surrounded by microtubules and a layer of endoplasmic reticulum. A unique organelle, the polar ring, is present at each pole; its junction is not clear. At metaphase the nuclear envelope is intact except for fenestrations at the poles. Spindle microtubules are attached to distinct kinetochores on the chromosomes and continuous pole-to-pole microtubules are present. The nucleolus has dispersed but, its granular components are still evident in the nucleoplasm. As the chromosomes separate, the nucleus elongates and finally constricts in the middle to produce 2 daughter nuclei.     

THE FINE STRUCTURE OF SPOROGENESIS IN THE XANTHOPHYCEAN ALGA PSEUDOBUMILLERIOPSIS PYRENOIDOSA1,2

The fine structure of vegetative cells, sporogenesis, and zoospores of the xanthophycean alga Pseudo-bumilleriopsis pyrenoidosa is described. Cleavage in sporogenesis closely resembles that of certain aquatic fungi.     

ISOLATION AND CHARACTERIZATION OF MYELIN-RELATED MEMBRANES

Abstract— Myelin related membrane fractions from rat brain and spinal cord were isolated from material normally discarded during standard myelin isolation procedures. A fraction which floated on 0.32 M-sucrose (F) and the material released after subjecting the myelin fraction to osmotic shock at two stages in the purification (W₁ and W₂) were characterized. These fractions were subjected to subfractionation on three step discontinuous sucrose gradients. Morphologically, the heavier subfrac-tions of W₁ and W₂ were shown to consist mainly of single membranes and vesicles. Sodium dodecyl sulphate (SDS) polyacrylamide gel electrophoresis showed that, relative to myelin, proteolipid and basic protein were reduced in all subfractions, while the high molecular weight proteins were increased. The specific activity of 2′,3′-cyclic nucleotide 3′-phosphohydrolase (CNP) was up to 2-fold higher than that of myelin in the heavier subfractions of W₁ and W₂. The major myelin-associated glycoprotein was also increased in these subfractions as determined by periodic acid-Schiff staining. Differential centrifugation of the initial tissue homogenate to remove microsomes prior to myelin isolation gave rise to W₁ and W₂ subfractions with a CNP specific activity 3–4 times that of myelin. The high molecular weight proteins and glycoproteins were enriched in these microsome-depleted subfractions, but were qualitatively similar to those of myelin. Some of the membranes in these fractions may be derived from the continuum between the plasma membrane of the oligodendrocyte and compact myelin. Fraction F consisted of small membrane fragments and many vesicles, and was particularly deficient in proteolipid. The specific activity of CNP in fraction F was about the same as myelin, while the major myelin associated glycoprotein could not be detected. Fraction F from normal CNS tissue appears to be similar to the floating fractions previously isolated in larger amounts from pathological brain undergoing edematous demyelination.     

ISOLATION AND CHARACTERIZATION OF GLYCOSAMINOGLYCANS IN PERIPHERAL NERVE AND SPINAL CORD OF MONKEY

—The isolation of uronic acid-containing glycosaminoglycans from peripheral nerve and spinal cord of monkey was done by combining the cetyl pyridinium procedure and DEAE-Sephadex column chromatography. The constituent analyses of the isolated GAG-fractions indicated that hyaluronic acid, chondroitin-4-sulphate, chondroitin-6-sulphate, heparan sulphate and a testicular hyaluronidase-resistant galactosamine-containing GAG were present in both tissues. Hyaluronic acid was the predominant GAG (63 per cent) in both tissues and its level was much higher than in brain. Chondroitin-4-sulphate constituted 16 per cent in both tissues. The levels of heparan sulphate and hyaluronidase-resistant galactosamine-containing GAG in these tissues were much lower than in brain. The results indicate that the patterns of GAGs in peripheral nerve and spinal cord of monkey are similar but differ from that of brain.     

酿酒酵母(Saccharomyces cerevisiae)基因启动子的分离和鉴定

用启动子探针型载体pFR109从酿酒酵母(Saccharomyces cerevisiae)总DNA中克隆到多个启动子片段,它们在大肠杆菌中均能启动β-半乳糖苷酶基因的表达。对其中Y8片段的进一步分析结果表明:该片段不仅来自酿酒酵母基因组,而且是以多拷贝的形式存在。当Y8片段再次转入供体酵母时,它仍能启动β-半乳糖苷酶基因表达,但经次克隆去掉Y8片段5′端部分顺序后,它就失去了启动子的功能。     

小定鞭藻毒素的分离与鉴定

从大量死鱼的鱼池中收集分离出小定鞭藻Ｐｒｙｍｎｅｓｉｕｍｐｏｒｖｕｍ的毒株,并在实验室成功地进行了单种培养,当温度２３℃,光照６００－８００ｌｘ盐度约１２—１６‰左右时,该藻在海水及人工海水培养基中均生长良好,在对数生长末期到平衡期溶血毒素活性最高。从藻细胞及浓缩的培养液中提取出二种毒素：溶血毒素（Ｈａｅｍｏｌｙｔｉｃｔｏｘｉｎｓ）和鱼毒素（Ｉｃｈｔｈｙｏｔｏｘｉｎｓ）。用新鲜牛血球测定了溶血毒素活性;用孔雀鱼测定了鱼毒素活性。用部分纯化的溶血毒素经元素分析、红外光谱、核磁共振及ＦＡＢ质谱测定,结果显示该藻溶血毒素可能是一个糖脂。     

ULTRASTRUCTURAL OBSERVATION OF CROSSWALLS IN THE BLUE-GREEN ALGA SPIRULINA MAJOR1,2

Spirulina major Kütz. was observed with the electron microscope and compared at the ultrastructural level with a species of Arthrospira. The presence, of crosswalls which develop by progressive ingrowth from peripheral walls was demonstrated in S. major. Since cellular septation is not consistent with the generally accepted characters of the genus Spirulina, a taxonomic shift may be indicated.     

STIMULATORY PROPERTIES OF FILTRATE FROM THE GREEN ALGA HORMOTILA BLENNISTA. I. DESCRIPTION1,2

A laboratory phenomenon involving autostimulation of growth by filtrates of the green alga Hormotila blennista is described, and stimulation attributed primarily to the secretion of organic metabolites. Filtrates obtained from actively growing cultures 1 through 4 weeks old showed maximum growth rate stimulation values in excess of 100%. Stimulatory properties of filtrate were heat labile, were not closely controlled by the starting pH within the limits normally encountered in culture, and did not result from depletion of essential nutrients. Concomitant with growth rate stimulation, filtrates characteristically extended the lag phase of culture growth. H. blennista filtrate can support bacterial growth and selectively stimulate or inhibit 2 planktonic green algae. It was suggested that extracellular organic products secreted by H. blennista during active growth could be of survival value to the organism, and could also play regulatory roles among other microorganisms in nature.     

REPRODUCTION AND SYSTEMATICS OF THE MARINE ALGA DERBESIA (CHLOROPHYCEAE) IN NEW ENGLAND1,2

The morphology, gross cytology, reproduction, and habitat ecology are described for Derbesia marina based on observations of New England field populations and laboratory cultures of this plant. These data, and additional observations on cultures of several other species of Derbesia from elsewhere and on type and other important collections, have been used to evaluate the systematic relationship of New England Derbesia with other species of this genus. The single Derbesia species in New England is referred to D. marina. The systematic criteria previously used to distinguish species within Derbesia are reviewed and interpreted within the context of the present investigation. In systematic studies, we stress the importance of the use of sporangial and chloroplast morphology, the presence or absence of pyrenoids, and reproductive history. Two types of life history are reported for D. marina in New England: (1) A form of D. marina collected at 20 m reproduces directly with stephanokontous zoospores growing into sporophytic plants of Derbesia morphologically identical to their parent thalli. (2) On the other hand, at least some New England, populations of D. marina have retained the genetic potential for producing a sexual generation (Halicystis ovalis), even though the latter is unknown for the coast of northeastern North America.³ Gametophytes (H. ovalis) were produced directly from enlargement and subsequent differentiation of uncleaved lateral sporangia in 2 cultured populations of New England D. marina. A single female and numerous male vesicles formed in this manner produced gametes, but neither fertilization nor parthenogenesis occurred; thus the entire life history was not completed in culture. The occurrence of the directly reproducing deep water form of D. marina is presented as evidence for speciation of a sporophyte (Derbesia) independent of its alternate gametophyte (Halicystis). An hypothesis is advanced to explain the source and means for expression of genetic variability necessary for speciation in a population of nonsexually reproducing Derbesia.     

红曲菌代谢产物中低极性组分的分离及表征

以石油醚∶醋酸乙酯 =4∶1(V/V)作为洗脱剂 ,采用柱层层析粗分离醇溶性红曲菌代谢产物中的低极性组分。经浓缩、结晶除去白色结晶后的浓缩液 ,用正己烷∶醋酸乙酯 =9∶1(V/V)作为展开剂进行薄层层析分离 ,在紫外灯下观察 ,从低极性组分中分离出六个组分 ,分别为 :具荧光组分、两个相隔较近的黄色组分、淡黄色具荧光组分、具浅蓝绿色荧光组分、具荧光组分。各组分的Rf 值分别为 :0 2 9、0 15、0 12、0 0 9、0 0 6、0 0 4。MS测定结果表明 ,Rf 值最大的具荧光组分可能为含有 OH及Br的共轭烯烃或脂肪酮 ,而在紫外灯下呈淡黄色组分为含有 OH的环状化合物。     

ISOLATION AND CHARACTERIZATION OF GLYCOSAMINOGLYCANS IN HUMAN BRAIN OF DIFFERENT AGE GROUPS

—Five distinct glycosaminoglycan fractions have been isolated from human brain of various age groups, by employing an improved fractionation procedure. Analysis of these fractions showed that human brain contains hyaluronic acid, chondroitin-4-sulphate, chondroitin-6-sulphate, dermatan sulphate, heparan sulphate and two unidentified low sulphated fractions. The pattern of variation of these compounds with age, indicates that they may be playing an important role in the process of myelination and brain maturation.     

中脑神经前体细胞的体外分离、培养和特性

为了解中脑神经前体细胞的体外培养特性和建立中脑神经前体细胞的体外分化调控机制提供细胞模型。本实验采用含有丝分裂源表皮生长因子(EGF)的无血清培养基培养来源于大鼠胚胎E14.5天的中脑神经前体细胞,应用免疫细胞化学方法了解其前体细胞特性。结果发现中脑神经前体细胞呈神经前体细胞特征性标记Nestin免疫染色阳性,无分化细胞标记;细胞克隆实验证实中脑神经前体细 胞有自我更新能力;在EGF刺激下增殖迅速;当撤去EGF后置于含胎牛血清的培养基和被覆多聚赖氨酸(PLL)的培养皿内,中脑神经前体细胞可分化成神经元和星形胶质细胞。本试验证明我们培养的中脑神经前体细胞具有增殖、自我更新能力和多向分化潜能特性。