黑桫椤孢子的无菌栽培

1植物名称黑桫椤(Alsophila podophylla Hook.)。2材料类别成熟的孢子。3培养条件培养基:(1)MS;(2)1/2MS;(3) 1/5MS;(4)1/10MS(1/2MS、1/5MS、1/10MS指大量和微量元素分别为MS基本培养基全量的1/ 2、1/5、1/10)。上述培养基均使用MS培养基     

Spore germination in Dictyostelium discoideum

Mutant spores of Dictyostelium discoideum, strain SG-10, differ from wild type spores in their ability to spontaneously germinate, to be activated with 5% dimethyl Sulfoxide (DMSO), and to be deactivated with 0.2 M sucrose. Both heat-activated wild type and mutant spores began to swell after a lag of 60–75 min at ambient temperature. Suspension of heat activated spores in 5% DMSO resulted in blockage of spore swelling and a concomitant severe inhibition of respiration; removal of 5% DMSO allowed resumption of respiration and the spores began to swell after a lag of only 15 min. It was concluded that 5% DMSO allowed the early reactions (M) to proceed but blocked the later reactions (R) of post-activation lag.Treatment of one day old spores with 20% DMSO solution for 30–120 min quantitatively activated the population. The post-activation lag time was directly dependent on the time of 20% DMSO treatment. Spores activated with 20% DMSO treatment could be deactivated by incubation at 0°C; the spores most quickly deactivated at 0°C were those within 10 min of swelling. Mitochondrial transport inhibitors such as azide and cyanide caused deactivation in an analogous manner. It is hypothesized that spores proceed to the second portion of the lag phase called (R) before the environment determines if dormancy is reimposed or if germination will proceed. The sensitive strain (SG-10) showed a greater degree of damage than the wild type after supraoptimal treatment with 40% DMSO. The spores became more resistant with age to the damaging action of 40% DMSO. All the observed effects of DMSO treatment were compatible with our multistate model of activation which suggests that the early portion of the lag phase (M) may involve a relative uncoupling of oxidative phosphorylation while the later portion (R) may require tight coupling.     

温度、基质对泡泡刺种子萌发的影响

研究了温度、种子大小和基质对荒漠植物泡泡刺种子萌发的影响.结果表明:无论是滤纸还是沙子基质上,泡泡刺种子的萌发率、平均萌发时间和萌发率指数受温度的影响显著,而受种子大小的影响不显著.在沙子处理中,较高的萌发率发生在恒温25℃～35℃和变温20℃/30℃,10℃时萌发率较低.平均萌发时间随着温度的上升而呈下降趋势.在滤纸和沙子基质中,泡泡刺萌发的基本温度、最佳温度和最高温度分别为9.0℃、25.3℃、45.2℃和4.8℃、34.1℃、45.0℃.从4.8℃～45℃,泡泡刺种子可萌发的热量范围广,说明了泡泡刺定植的高度潜力.在荒漠生态系统恢复中,这种特性可使泡泡刺成为较好的候选者.     

Photocontrol of seed germination in Impatiens wallerana Hook. f.

General characteristics of light sensitivity of Impatients wallerana seeds were investigated. Germination was absolutely dependent on light, irrespective of temperature. High percentages of germination were obtained by exposure to long periods of illumination or, alternatively, to several repeated short irradiations with red light. In this case, responsiveness to light was not altered by increasing either the initial incubation period in darkness or the dark intervals between short exposures. Effects of red light were reversed by far-red light, thus demonstrating the involvement of phytochrome. Evidence was presented for an interactive effect, of unknown physiological nature between red and far-red light on the germination of the seeds.Abbreviations P_r phytochrome, red light absorbing form - Pfr phytochrome far-red absorbing form     

Spore germination inCylindrospermum sp.: Influence of gases and growth conditions

Influence of different gases on spore germination ofCylindrospermum sp. revealed that acetylene and ethylene suppressed the germination which was more pronounced at their higher concentrations. Germination was completely inhibited under the atmosphere of hydrogen and argon even when supplied with 1% CO₂. Carbon dioxide, both in air and in N₂, stimulated the process. However, higher concentrations of CO₂ inhibited the germination in a concentration-dependent manner, possibly due to a decrease in pH. Germination was completely arrested in the absence of light and nutrients. The energetic requirement for germination was not efficiently fulfilled by photosystem I (PS II was blocked by 3-(3,4-dichlorophenyl)-1,1-dimethylurea) or under conditions of anoxygenic photosynthesis (medium supplemented with sodium sulfide).     

Spore pool glutamic acid as a metabolite in germination

Spore glutamic acid pools were examined in dormant and germinating spores using colorimetric and (14)C analytical procedures. Germination of spores of Bacillus megaterium (parent strain), initiated by d-glucose, was accompanied by a rapid drop in the level of spore pool glutamate, from 12.0 mug/mg of dry spores to 7.7 mug/mg of dry spores after 30 sec of germination. Similar decreases in extractable spore pool glutamate were observed with l-alanine-initiated germination of B. licheniformis spores. On the other hand, glutamate pools of mutant spores of B. megaterium, with a requirement of gamma-aminobutyric acid for spore germination, remained unchanged for 9 min of germination, at which time more than 50% of the spore population had germinated. Evidence for conversion of spore pool glutamate to gamma-aminobutyric acid during germination of spores of B. megaterium (parent strain) was obtained.     

Spore lytic enzyme released from Clostridium perfringens spores during germination.

The exudate of fully germinated spores of Clostridium perfringens was found to contain a large amount of a spore lytic enzyme which acted directly on alkali-treated spores of the organism to cause germination. Although no detectable amount of the enzyme was found in dormant spores during germination in a KCl medium, the enzyme was produced rapidly and released into the medium. The optimal conditions for enzyme activity were pH 6.0 and 45 degrees C. Maximum activity occurred in the presence of various univalent cations at a concentration of 50 mM. The enzyme was readily inactivated by several sulfhydryl reagents. A strong reducing condition was generated in the ionic germination of the spores, a minimum Eh level of -350 mV being reached 30 min after initiation of germination. Furthermore, adenosine triphosphate-dependent pyruvate:ferredoxin oxidoreductase (EC 1.2.7.1) was identified in both dorman and germinated spores. The relationship between the release of active enzyme and the generation of reducing conditions during germination is discussed.     

Spore germination promoter of Dictyostelium discoideum excreted by Aerobacter aerogenes.

The nutrient medium in which Aerobacter aerogenes was grown, contains a spore germination promoter (SGP) for the cellular slime mould Dictyostelium discoideum. SGP can cuase synchronous spore germination in a short time, and triggers the germination process in just a few minutes. Germination-promoting capacity of SGP decreases as it comes in contact with increasing number of spores. When spores activated by SGP are stored at 4 degrees C, they gradually return to the dormant state. SGP is comparatively heat-stable, but is unstable at pH above 10 or under 3.     

Spore germination and isozyme patterns in the apomictic fern Cyrtotnium falcatum

Progeny from a plant of the apomictic species Cyrtomium falcatum were examined by protein electrophoresis. These progeny were produced from spores originating in sporangia with differing spore numbers. Analysis of zymograms indicates that variant banding patterns were exhibited in 16.1% of the progeny sampled. These anomalous phenotypes suggest that some apomictically reproducing plants can produce genetically variable progeny.     

Spore germination in Dictyostelium discoideum: I. The thermodynamics of reversible activation

Spore activation in Dictyostelium discoideum is characterized by a narrow range of activation temperatures centered near 43 °C. The temperature required for maximal spore activation may vary from one to two degrees depending upon the sporulation temperature and the age of the spore preparation. Thermodynamic calculations revealed that spore activation might involve a greater enthalpy and entropy change than that expected for soluble globular protein denaturation. The number of activation sites was calculated to be nine or more per spore using assumptions based upon a Poisson distributed array of sites. A hypothesis is suggested that the activation “site” is the mitochondrion and that the inner mitochondrial membrane contains regulatory proteins (“subsites”) which may restrict oxidative phosphorylation in the dormant spore. The restriction imposed upon oxidative phosphorylation may be relaxed upon partial denaturation of the “subsites” resulting in spore activation and subsequent germination.     

Spore morphology and some other features of Goniomitrium Hook. & Wils. (Funariaceae)

Abstract

Goniomitrium enerve, G. acuminatum and G. africanum are distinguished mainly on costal features. There are some problems with the Australian species because of intergradation of characters but no name changes have been suggested and a key to species is provided. The spores of the three species, which are monolete and have a large reticulate ornamentation, are distinctive amongst moss spores and appear to be diagnostic for the genus.     

Spore germination and mycelial growth of streptomycetes at different humidity levels

This study is the first to show the ability of streptomycetes to develop at a very low humidity level. All of the streptomycetes studied produced growth at low humidity (aw 0.86 and 0.67). This capacity was most markedly pronounced in Streptomyces odorifer, whose spores were capable of germinating, and mycelial germs increased in length, at the air humidity aw 0.50. The formation of lateral branches (mycelium branching) at this humidity was noted only in single S. odorifer germs and only after 72 h of incubation. Study of streptomycete growth on an agarized medium with different osmotic pressures, created by various glycerol concentrations in the medium, showed that, at aw 0.67, the spores of all the streptomycetes studied germinate, producing mycelial germs but not microcolonies. The ecological significance of mycelial prokaryotes in soil microbial communities that develop and function under conditions of extremely low humidity is discussed.     

Spore germination and swarm cell morphogenesis in the acellular slime mold Fuligo septica

This report describes conditions under which spores of the acellular slime mold Fuligo septica underwent a very rapid, synchronous and complete (100%) germination followed by morphogenesis of motile, flagellated swarm cells from the released protoplasts. This developmental sequence was initiated immediately upon wetting the spores with a surfactant and was completed within 40–50 min in the absence of any exogenous nutrient other than sodium phosphate buffer. Oxygen was required for germination. The rate and percentage of germination diminished with increasing spore concentration suggesting the existence of an autoinhibitor. The morphological sequence of events in the differentiation process was examined by scanning electron microscopy.