DNA extraction conditions fromPorphyra perforata using LiCl

A rapid and economical method of DNA extraction from a red seaweedPorphyra perforata J. Agardh has been developed by the use of lithium chloride. This paper describes the optimization of extraction conditions. Heat treatment of tissues in a solution (0.8 M LiCl, 0.6% Sarkosyl, 10 mM EDTA, 0.2% PVPP, 5% ß-mercaptoethanol, pH 9.0) at 55 °C for 10 min extracts DNA that is of sufficient quality to be used as a template for PCR amplification. Total DNA yield was approximately 30 to 50g g^–1 t of partially dried tissue. Total RNA yield was approximately 400g g^–1 of partially dried tissue. Carbohydrate was contained as approximately 40 to 90 mM (expressed as glucose equivalents) from 1 g tissue, and protein contamination calculated as the O.D. 260/280 ratio was in the range of 1.4 to 1.7. The DNA was characterized by high molecular weight larger than 50 kb.     

An evaluation of species relationships in the Porphyra perforata complex (Bangiales,Rhodophyta) using starch gel electrophoresis

Traditional morphological features have formed the basis for distinguishing species of Porphyra. Among these features are number of cell layers, number of chloroplasts per cell, arrangement of reproductive structures on the thallus, and overall morphology. Chromosome number and chromosome morphology have helped corroborate some species identities. A survey of northeast Pacific species of Porphyra using starch gel electrophoresis of 15 soluble proteins has shown that electrophoretic banding patterns provide a reliable diagnostic tool for species identification. Data from starch gel electrophoresis are presented to confirm the identities of species formerly associated with the Porphyra perforata species-complex in British Columbia and northern Washington. Porphyra abbottae, P. fallax, P. kanakaensis, and P. torta are recognized as distinct species, and Porphyra sanjuanensis is synonymized with P. perforata.     

Conchospore production and seasonal occurrence of some Porphyra species (Bangiales,Rhodophyta) in Washington State

The leafy thalli of species of the marine red algal genus Porphyra grow rapidly but persist for a relatively short time on rocky intertidal or subtidal substrata or as epiphytes on other marine plants. In most species, the large, short-lived leafy thalli alternate with small, presumably perennial, filamentous conchocelis plants. Depending on the species of northeastern Pacific Porphyra, photoperiod and temperature are important regulators of conchospore formation and release. Data from laboratory studies of conchospore formation and release in five Washington species of Porphyra (P. abottae, P. nereocystis, P. perforata, P. pseudolanceolata and P. torta) indicate that conchospores are most likely to be released at a time that precedes the appearance of the leafy thalli in the field.     

Protoplast isolation and regeneration in the marine red alga Porphyra nereocystis

We have developed a method for isolating viable protoplasts from the blade phase of the epiphytic marine red alga Porphyra nereocystis Anderson, using a two-step enzymatic digestion with commercially available enzymes. The first step uses papain, the second step uses abalone acetone powder. The method is rapid and gives a high yield of viable protoplasts. In liquid culture in enriched seawater medium, the protoplasts can undergo regeneration along three pathways: they directly form filaments resembling the conchocelis phase of Porphyra; they form calli with relatively thick-walled, pigmented cells; and they indirectly form blades from the edges of these calli. Porphyra nereocystis protoplasts also may serve as an alternative propagation method in aquaculture and be useful for studies of cell-wall formation, cell division, and thallus differentiation. They may also be used in somatic selection, somatic hybridization and gene-transfection experiments.Abbreviations AAP abalone acetone powder - PAP papain - FDA fluorescein diacetate This paper is dedicated to the memory of the late Dr. Munenao Kurogi (1921–1988), Professor Emeritus of Hokkaido UniversityThis research was supported by the Washington Sea Grant Program (National Oceanic and Atmospheric Administration). We thank Professor Y. Fujita (Nagasaki University, Japan), Professor S.-J. Wang (Shanghai University of Fisheries, P.R. China) and Dr. H. Kito (Seikai Regional Fisheries Research Laboratory, Nagasaki, Japan) for sharing their experience with Porphyra protoplast production with us. We thank J.S. Charleston for expert technical assistance in preparation of the electron-microscopy specimens. We also thank Dr. S.K. Herbert and John Carrier (Friday Harbor Laboratories) and Dr. John Merrill and D. Gillingham (American Sea Vegetable Co. and Applied Algal Research, Seattle) for collections of P. nereocystis.     

Life cycle of Porphyra vietnamensis Tanaka & Pham-Hoang Ho from Thailand

Porphyra vietnamensis Tanaka & Pham-Hoang Ho is a tropical species of high potential for farming. Studies of the life cycle have been conducted for many years but have not been successful until recently. Mature thalli were collected from Songkhla, in the southern part of Thailand, and were used to obtain Conchocelis in the laboratory in Bangkok. Conchocelis in shells as well as free-floating filaments could be observed after one week of incubation at 25 °C, 25 salinity and 350–500 lux light intensity, and covered the culture shell surface within 2 months. Conchosporangia were formed after being incubated for 10 days at 30 °C, 20 salinity under light intensities of 350–500 lux with a photoperiod of 12 hours a day. Induction of conchospore release was achieved by lowering the temperature to 25 °C and the salinity to 10–15 and increasing the light intensity to 800–1000 lux. Liberated conchospores germinated into young thalli which became mature after 70 days.     

Nori cultivation in North America: growth of the industry

The cultivation of the red alga Porphyra in North America to produce the edible product nori is now in its tenth year of development. Cultivation technology has been transferred and modified from Japan and Korea. Early efforts by the Washington State Department of Natural Resources indicated that cultivation is biologically feasible and could be economically viable. Commercial production has begun in Washington, U.S.A. and in British Columbia, Canada. Early products are of high quality. Constraints to more rapid development are institutional — obtaining necessary permits for use of water areas and financing is difficult.This paper is dedicated to the memory of Bud Brinkhuis — friend and fellow phycologist who will be missed by all of us growing seawwees.     

Phycological research in the development of the Chinese seaweed industry

The term seaweed industry is employed in a broad sense and includes production both of commercial seaweeds such as Laminaria and Porphyra by phycoculture and of processed seaweed products, such as algin, agar and carrageenan.Before the founding of the People's Republic, China had a very insignificant seaweed industry, producing small quantities of the purple laver Porphyra and the glueweed Gloiopeltis by the primitive rock-cleaning method and the kelps Laminaria and Undaria by the primitive stone-throwing method, both aiming at enhancing the growth of the wild seaweeds. Also, a small quantity of agar was manufactured by the traditional Japanese method of gelling, freezing, thawing and drying the product. The small production was not sufficient to meet the demand of the Chinese people who for ages have appreciated seaweeds and their products for food. Therefore, large quantities of seaweeds and seaweed products had to be imported from various countries, for instance, Eucheuma and Gracilaria from Indonesia and other southeastern Asian countries, Laminaria and agar from Japan, even Porphyra from the USA. Annual Laminaria import from Japan generally amounted to over 10 000 tons and in some years approached 20 000–30 000 tons. Some quantities of the glueweed Gloiopeltis and the vermifuge weed Digenea simplex were exported, mainly to Japan.Since the founding of the People's Republic of China in October, 1949, China has exerted efforts to build up a self-supporting seaweed industry. Now after a lapse of 30-some years, a sizable seaweed industry has been developed. China is now able to produce by phycoculture more than one million tons of fresh seaweeds, including Laminaria, Undaria, Porphyra, Eucheuma, Gracilaria etc. and several thousand tons of seaweed extracts, including algin, agar, carrageenan, mannitol and iodine. At present, China still imports some quantities of seaweeds and seaweed products from various countries but is able to produce sufficient quantities to meet the people's need and even to export some quantities of the seaweeds Laminaria, Undaria and Porphyra and the seaweed products algin and mannitol.At the Tenth International Seaweed Symposium, I presented a paper on the Marine Phycoculture of China, in which I emphasized on the methods of cultivation (Tseng 1981b). Therefore I would like to take this opportunity to supplement the last lecture by presenting a paper on the role of phycological research in the development of China's seaweed industry.     

Effect of harvest method and timing on yield and regeneration of Karengo (Porphyra spp.) (Bangiales,Rhodophyta) in New Zealand

Commercial interest in harvesting wild stocks ofPorphyra and concern for this prized resource by the Maori community highlighted the need to investigate the impact of harvest method and timing onPorphyra beds. Harvesting trials were carried out at two locations near Kaikoura (South Island) and one in Wellington (southern North Island) between June 1987 and September 1987. At each of five sampling sites, ten replicate sets of four quadrats were used to test the effects of harvest method and timing on yield and regeneration. The method of harvest had a major effect on the extent of regeneration: in quadrats in which thePorphyra had been cut with basal portions left intact there were harvestable plants within two months, whereas in quadrats which were cleared of allPorphyra there was very little growth after the same period. Harvests in the latter half of thePorphyra growing season gave greater yields at all sites except Wellington. Several species ofPorphyra were found to exist at the Kaikoura sampling sites and a single, different, species at the Wellington site. There were site to site differences in the yields.     

携带TRAIL的溶瘤腺病毒联合LiCl对癌细胞的生长抑制效应

研究糖原合成激酶3的抑制剂LiCl联合携带TRA／L基因的溶瘤腺病毒Ad．sp—ElA—E1B（△55kDa）．TRAIL—Flag（Ad．sp—TRAIL—Flag）对癌细胞的体外杀伤作用。采用MTT法检测癌症特异性病毒Ad．sp—TRAIL—Flag联合药物LiCl对三种癌症细胞株的生长抑制作用;通过结晶紫实验进一步检测联合用药的杀伤效果：进而通过Western blot实验检测联合作用对癌细胞中TRAIL蛋白表达的影响,最后通过流式细胞仪检测其对癌细胞的凋亡作用。结果显示,LiCl联合Ad．sp—TRAIL．Flag的处理对癌细胞的增殖抑制作用明显优于两者单独使用。Western blot实验证明,LiCl可提高溶瘤腺病毒Ad．sp—TRAIL—FIag处理后TRAIL蛋白的表达水平,从而增强了溶瘤腺病毒Ad．sp—TRAIL—Flag通过乃己4儿的信号通路的杀伤效果。     

Effect of seaweed concentrate on the establishment and yield of greenhouse tomato plants

Seaweed concentrate prepared fromEcklonia maxima (Osbeck) Papenfuss, when applied as a soil drench, significantly improved the growth of tomato seedlings. Application as a foliar spray had no effect on young plants. In a second experiment SWC-treated plants exhibited early fruit ripening and a total fruit fresh weight increase of 17%. The number of harvested fruit were improved by about 10%. In this instance foliar applied SWC was more beneficial than SWC applied to the soil. The significance of these findings is discussed.author for correspondence     

Influence of tissue source and growth rates on dry weight and carrageenan composition of Chondrus crispus (Gigartinales,Rhodophyta)

Carrageenan analyses were conducted on vegetative female clones of Chondrus crispus that were cultured to provide tissues with differing growth rates. Tissue dry weights increased from apex to base of fronds. Total carrageenan contents were lower in apical 1 to 2 cm segments than elsewhere in the frond, except when the alga was grown at high photon irradiances. Clone 373A contained more carrageenan than clone G8. The proportion of 0.3 M KCl-soluble polymers in the total native carrageenans varied from 44 to 92%, being highest in older tissues of fronds cultured at high photon irradiances. The apical 1 cm segments contained less KCl-soluble carrageenans than other tissues from the corresponding fronds. The KCl-soluble carrageenans, when alkali-modified and refractionated, afforded the expected kappa-iota carrageenan in > 79% yields. The remainder consisted of a polymer containing 23.1% SO₃Na and 8.4% 3,6-anhydrogalactose. Lambda carrageenan was not detected. Variations in carrageenan distribution between the apical region and other parts of the frond may reflect the increasing influence of medullary tissue developed as the immature cells differentiate.     

Effect of a phorbol ester on basic surface properties of trichomonads

The effect of nanomolar concentrations of 12-O-tetradecanoil-phorbol-13-acetate (TPA) on the cell surface of the urogenital parasitic protozoaTrichomonas vaginalis andTritrichomonas foetus was evaluated by means of measurements of the parasites’ surface tension, electrokinesis, lectin agglutination tests, and adhesion to inert substrates. TPA-treated parasites had their adhesion increased to both plastic and glass substrates. This was accompanied by increases in the parasites’ net negative surface charge and also by changes in their surface tension. The lectin agglutination assays suggest that the increase in surface negativeness may be related in some extent to alterations in the oligosaccharide composition. Successive treatment of the microorganisms with TPA and sphingosine, a well-known competitive inhibitor of the phorbol ester active site, depressed the tendency of trichomonads to exhibit a phenotype of activated cells.