堆肥处理对污泥腐殖物质形态及其重金属分配的影响

采用透析、凝胶色谱 (SephadexG 75 )研究了污泥堆肥前后腐殖质分子大小的变化及重金属Cu和Zn在各级组分中的分配。透析结果表明 ,污泥经过堆腐以后 ,腐殖质中小分子物质 (<10 0 0Da)组分的含量下降 6 4 % ,而相对高分子组分 (>2 5 0 0 0Da)却增加了 6 8%。凝胶色谱进一步证实 ,污泥经过 4 9d堆腐后 ,腐殖质中大于 2 0 0 0KDa的大分子组分是堆肥起始时的2 3倍。而小分子组分明显减少 ,表现在小分子组分的凝胶洗脱体积明显减少。堆肥腐熟以后 ,腐殖质吸附的Cu、Zn元素含量增加 ,其中Cu主要被吸附在大分子物质上 ,而Zn主要与小分子物质结合     

淀粉合酶的酶学与分子生物学研究进展

淀粉合酶作为淀粉合成的关键酶之一,一直是淀粉研究的重要内容,这些研究多集中在对其同工型的研究,淀粉合酶的两类主要同工型分别为淀粉粒结合的淀粉合酶和可溶性淀粉合酶,这两类同工型的作用极为复杂,本文介绍了淀粉合酶同工型的酶学和分子生物学近年来的研究进展,同时也讨论了这些同工型的分类,相互关系及其在淀粉合成过程中的生理功能等内容。     

Factors affecting the distribution and abundance of an unpigmented heterotrophic alga Prototheca richardsi

1. Numbers of the contramensal alga Prototheca richardsi were high in spring in two ponds used for breeding by anuran amphibians, but lower at other times of year and undetectable in two ponds not used by anurans. 2. Prototheca richardsi became abundant in the silt of eight experimental ponds which contained tadpoles, but remained undetectable in four otherwise identical ponds lacking tadpoles. 3. Prototheca richardsi numbers in laboratory microcosms remained stable for many days in sterile tap water, but declined with a half-life of about 6 days in pond water at 20°C. 4. Further studies with microcosms using antibiotics and electron microscopy indicated that mortality of P. richardsi was caused primarily by pathogenic bacteria.     

DETECTION OF CLOSTRIDIUM BOTULINUM TYPE E TOXIN BY MONOCLONAL ANTIBODY ENZYME IMMUNOASSAY

Botulinum type E toxin is a well recognized causative agent of seafood botulism poisoning. Underprocessing or postretort recontamination of preserved seafoods has resulted in sporadic cases of botulism. Currently, laboratory mice are being used to detect this toxin. However, it requires three to six days to obtain final results. A rapid method using monoclonal antibody (Mab) enzyme immunoassay was therefore developed. Hybridomas secreting specific Mab against the type E epitope were generated by fusion of SP/20-Ag 14 myeloma cells with spleen cells from BALB/c mice immunized with botulinum type E neurotoxoid. Five potent, stable hybridomas were selected, cloned, propagated, and preserved in liquid nitrogen as cell lines. Immunoglobulin subisotyping showed these Mabs belonged to the IgG subclasses. No cross-reaction was observed with culture supernatants of C. botulinum types A, B, and F or with crude toxins extracts of type C and D. Large quantities of Mabs were produced in ascites fluids, harvested, and affinity purified. A Mab-based biotin-avidin amplified double sandwich enzyme-linked immunosorbent assay allowed detection of type E toxin in inoculated seafoods at levels equivalent to 1–10 MLDs/ml (5–10 pg/ml).     

Pseudomonas tolaasii in cultivated mushroom (Agaricus bisporus) crops: effects of sodium hypochlorite on the bacterium and on blotch disease severity

Sodium hypochlorite killed Pseudomonas tolaasii in water in 30 s at pH 6.0 when 5 mg/1 free available chlorine (FAC) was used. On glass beads 62.5 mg/1 FAC was necessary to kill the pathogen in 30 s. Peat and limestone mixture ('casing') prevented some cells of the pathogen being killed by chlorine. Casing treated with 50 and 100 mg/1 FAC still contained some Ps. tolaasii cells which were later able to multiply. Although some viable cells of the pathogen survived the use of 150 mg/1 FAC these were apparently unable to multiply. Mushroom tissue is more 'disinfectant-wasting' than casing, the pathogen on it surviving 250 mg/1 FAC for 10 min. In controlled environmental experiments, use of 150 mg/1 FAC at mushroom 'pinning' (2.5 mm diameter primordia) gave as much control of blotch disease as was obtainable if chlorination began after casing. Delay in starting chlorination until the mushrooms were 10 to 15 mm in diameter resulted in blotch disease incidence and severity as severe as in unchlorinated controls. Disease incidence was not reduced when 50, 100 and 150 mg/1 FAC was used, but disease severity was significantly reduced when 150 mg/1 was used. Adjusting the pH of the water did not affect these results. On commercial farms, routine watering with 150 mg/1 FAC starting at pinning, checked frequently by the sodium arsenite titrimetric method, for 3 years, reduced the percentage of mushrooms discarded because of very severe Ps. tolaasii blotch from 5.2% to 0.6% on one farm and from 7.4% to 0.5% on another, but did not eliminate the disease completely.