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1.
Germination of Agaricus bisporus spores is stimulated by vapourdiffusing from dilute solutions of various short-chain fattyacids, especially uo-valeric acid. No increase in germinationwas found in spores treated with succinic acid. All these compoundsinhibited spore germination at concentrations above the optimallevel. An examination of the influence of hydrogen-ion concentrationon germination is also reported. It is suggested that the germination-stimulatingactivity of the acids tested is not a pH effect but is due todirect entry of these compounds into metabolic pathways, particularlythose of fat metabolism. The prominent oil reserves in thesespores suggests a system analogous to that of rust uredospores,the respiration and germination of which is stimulated by short-chainfatty acids, contributing both to the respired carbon dioxideand the for-mation of new cell materials. 相似文献
2.
Optimum germination of spores of a Fissidens species occurredat a relatively higher temperature (30 °C) than the optimumgermination of those of a Racopilum species (25 °C). Subsequentprotonemal growth of the two mosses also showed the same differentialtemperature optima. The high-temperature requirement for germinationof Fissidens spores happens to coincide with the maturationand dispersal of the spores in the dry season, and apparentlyfavours the establishment of new shoots. Fissidens sp, Racopilum sp, tropical mosses, spore germination, temperature adaptation 相似文献
3.
Moeller R Horneck G Rettberg P Mollenkopf HJ Stackebrandt E Nicholson WL 《Current microbiology》2006,53(3):227-231
RNA was extracted from dormant and germinating Bacillus subtilis 168 spores (intact spores and chemically decoated spores) by using rapid rupture followed by acid–phenol extraction. Spore
germination progress was monitored by assaying colony forming ability before and after heat shock and by reading the optical
density at 600 nm. The purity, yield, and composition of the extracted RNA were determined spectrophotometrically from the
ratio of absorption at 260 nm to that at 280 nm; in a 2100 BioAnalyzer, giving the RNA yield/108 spores or cells and the distribution pattern of rRNA components. The method reported here for the extraction of RNA from
dormant spores, as well as during different phases of germination and outgrowth, has proven to be fast, efficient and simple
to handle. RNA of a high purity was obtained from dormant spores and during all phases of germination and growth. There was
a significant increase in RNA yield during the transition from dormant spores to germination and subsequent outgrowth. Chemically
decoated spores were retarded in germination and outgrowth compared with intact spores, and less RNA was extracted; however,
the differences were not significant. This method for RNA isolation of dormant, germinating, and outgrowing bacterial endospores
is a valuable prerequisite for gene expression studies, especially in studies on the responses of spores to hostile environmental
conditions. 相似文献
4.
Spore Germination Patterns in the Ferns, Cyathea and Dicksonia 总被引:1,自引:0,他引:1
Cell division patterns during germination of spores of Cyatheaaustralis, C. cooperi and Dicksonia antarctica were examinedby light microscopy of sectioned materials and by the scanningelectron microscope. In C. australis and C. cooperi the rhizoidwas traced to a small cell formed by an asymmetric divisionof the spore by a wall parallel to its equatorial plane. Incontrast, the rhizoid was formed by a division of the sporeparallel to its polar axis in D. antarctica. In spores of bothgenera, a second division wall oriented in a plane perpendicularto the first gave rise to the protonemal cell. Certain aspectsof germination described here in spores of Cyathea and Dicksoniaare in conflict with the published accounts of spore germinationin these genera. Cyathea, Dicksonia, spore germination, cell division pattern 相似文献
5.
Sugai Michizo; Tomizawa Ken-ichi; Watanabe Masakatsu; Furuya Masaki 《Plant & cell physiology》1984,25(2):205-212
An action spectrum between 250 and 800 nm for the inhibitionof red-light-induced germination of spores in the fern Pterisvittata was determined on the Okazaki Large Spectrograph. Theresultant spectrum showed prominent peaks of effectiveness atabout 370, 440 and 730 nm and a minor peak in the neighborhoodof 260 nm. Next, a brief red light irradiation was given immediatelyafter the monochromatic irradiation to cancel the inhibitoryeffect caused by simultaneously formed PR. This resulted ina complete disappearance of the peak at 730 nm and considerabledecrease of other peaks in the shorter wavelength region exceptat 260 nm. Further correction of the latter spectrum by consideringthe transmission spectrum of a spore coat revealed that 260nm light acted more effectively than lights of 370 and 440 nm.The inhibitory effect of UV light on spore germination was nullifiedby subsequent irradiation with red light for 24 h or darknessfor 48 h followed by a brief red irradiation, indicating thatthe inhibitory action of UV light was ascribable to a blue-ultraviolet light-absorbing pigment.
4Present address (KT) and permanent address (MF): Botany Department,Faculty of Science, University of Tokyo, Hongo, Tokyo 113, Japan. (Received July 30, 1983; Accepted November 21, 1983) 相似文献
6.
The spores of Anabaena doliolum formed in light (light spores)and after transfer to darkness (dark spores) are biochemicallydifferent in that the light spores contain chlorophyll a andphycocyanin, while dark spores seem to lack them. The apparentbiosyntheses accompanying dark-spore germination seem to proceedin the following order: RNA, chlorophyll a, phycocyanin andDNA. Results of chloramphenicol treatment indicate that proteinsynthesis precedes RNA synthesis. The biosynthetic events followingRNA synthesis show a requirement for light. 相似文献
7.
PHOTOMORPHOGENESIS IN PTERIS VITTATA: I. PHYTOCHROME-MEDIATED SPORE GERMINATION AND BLUE LIGHT INTERACTION 总被引:1,自引:0,他引:1
- Spores of the fern Pteris vittata did not germinate under totaldark conditions, while an exposure of the spores to continuouswhite light brought about germination. The germination was mosteffectively induced by red light and somewhat by green and far-red,but not at all by blue light. The sensitivity of spores to redlight increased and leveled off about 4 days after sowing at2728. The promoting effect of red light could be broughtabout by a single exposure of low intensity. Far-red light givenimmediately after red light almost completely reversed the redlight effect, and the photoresponse to red and far-red lightwas repeatedly reversible. The photoreversibility was lost duringan intervening darkness between red and far-red irradiations,and 50% of the initial reversibility was lost after about 6hr of darkness at 2728. These observations suggest thatthe phytochrome system controls the germination of the fernspore.
- When the imbibed spores were briefly exposed to a low-energyblue light immediately before or after red irradiation, theirgermination was completely inhibited. The blue light-inducedinhibition was never reversed by brief red irradiation givenimmediately after the blue light. The escape reaction of redlight-induced germination as indicated by blue light given aftervarious periods of intervening darkness was also observed, andits rate was very similar to that determined by using far-redlight. Spores exposed to blue light required 3 days' incubationin darkness at 2728 to recover their sensitivity tored light. The recovery in darkness of this red sensitivitywas temperature-dependent. It is thus suggested that an unknownbluelight absorbing pigment may be involved in the inhibitionof phytochrome-mediated spore germination.
8.
Taejun Han Jeong‐Ae Kong Young‐Seok Han Sung‐Ho Kang Donat‐Peter Hder 《Journal of phycology》2004,40(2):315-322
Recent reduction in the ozone shield due to manufactured chlorofluorocarbons raised considerable interest in the ecological and physiological consequences of UV‐B radiation (λ=280–315 nm) in macroalgae. However, early life stages of macroalgae have received little attention in regard to their UV‐B sensitivity and UV‐B defensive mechanisms. Germination of UV‐B irradiated spores of the intertidal green alga Ulva pertusa Kjellman was significantly lower than in unexposed controls, and the degree of reduction correlated with the UV doses. After exposure to moderate levels of UV‐B irradiation, subsequent exposure to visible light caused differential germination in an irradiance‐ and wavelength‐dependent manner. Significantly higher germination was found at higher photon irradiances and in blue light compared with white and red light. The action spectrum for photoreactivation of germination in UV‐B irradiated U. pertusa spores shows a major peak at 435 nm with a smaller but significant peak at 385 nm. When exposed to December sunlight, the germination percentage of U. pertusa spores exposed to 1 h of solar radiation reached 100% regardless of the irradiation treatment conditions. After a 2‐h exposure to sunlight, however, there was complete inhibition of germination in PAR+UV‐A+UV‐B in contrast to 100% germination in PAR or PAR+UV‐A. In addition to mat‐forming characteristics that would act as a selective UV‐B filter for settled spores under the parental canopy, light‐driven repair of germination after UV‐B exposure could explain successful continuation of U. pertusa spore germination in intertidal settings possibly affected by intense solar UV‐B radiation. 相似文献
9.
Vegetative cells of Bacillus cereus Strain T contain cytochromeb-562, a minor b-type component, in addition to known components,cytochrome a+a3, cytochrome b-557 and cytochrome c-551. Also,the spores contain low but definite amounts of cytochromes b-562and c-551, which were oxidized when the spores were shaken withair. Contents of cytochromes a, b and c per cell and per cellnitrogen, and the activity of glucose oxidation increased duringspore germination and elongation. During the stage precedingfirst cell division, cytochrome contents per cell increasedin parallel with the increase of cell nitrogen, while the activityof glucose oxidation decreased. During early exponential growth,the content of cytochrome b per cell nitrogen and respiratoryactivity with glucose again increased. When cells entered thesporulation stage, characterized by structural changes insidethe cells, the activity of glucose oxidation began to decrease,while that of acetate or succinate oxidation started to increase.During the sporulation process, the contents of the three cytochromecomponents continued to increase and reached the highest levelin cells containing completed spores, but the activity of respirationwith endogenous or added substrates was negligible in thesecells. (Received November 10, 1975; ) 相似文献
10.
Gene Activity during Germination of Spores of the Fern, Onoclea sensibilis: RNA and Protein Synthesis and the Role of Stored mRNA 总被引:1,自引:0,他引:1
Pattern of 3H-uridine incorporation into RNA of spores of Onocleasensibilis imbibed in complete darkness (non-germinating conditions)and induced to germinate in red light was followed by oligo-dTcellulose chromatography, gel electrophoresis coupled with fluorographyand autoradiography. In dark-imbibed spores, RNA synthesis wasinitiated about 24 h after sowing, with most of the label accumulatingin the high mol. wt. poly(A)RNA fraction. There was noincorporation of the label into poly(A) + RNA until 48 h aftersowing. In contrast, photo-induced spores began to synthesizeall fractions of RNA within 12 h after sowing and by 24 h, incorporationof 3H-uridine into RNA of irradiated spores was nearly 70-foldhigher than that into dark-imbibed spores. Protein synthesis,as monitored by 3H-arginine incorporation into the acid-insolublefraction and by autoradiography, was initiated in spores within12 h after sowing under both conditions. Autoradiographicexperiments also showed that the onset of protein synthesisin the cytoplasm of the germinating spore is independent ofthe transport of newly synthesized nuclear RNA. One-dimensionalsodium dodecyl sulphate-polyacrylamide gel electrophoresis of35S-methionine-labelled proteins revealed a good correspondencebetween proteins synthesized in a cell-free translation systemdirected by poly(A) +RNA of dormant spores and those synthesizedin vivo by dark-imbibed and photo-induced spores. These resultsindicate that stored mRNAs of O. sensibilis spores are functionallycompetent and provide templates for the synthesis of proteinsduring dark-imbibition and germination. Key words: Onoclea sensibilis, fern spore germination, gene expression, protein synthesis, sensitive fern, stored mRNA 相似文献
11.
Laboratory and field experiments involving Asplenium ruta-murariaL., Asplenium trichomanes L. subsp. quadrivalens D.E. Meyeremend. Lovis and Asplenium scolopendrium L. [= Phyllitis scolopendrium(L.) Newm.] revealed differences in their temperature requirementsfor germination and in their sexual development on soil. Thegermination responses of A. trichomanes and A. scolopendriumto culture temperatures of 10, 15, 20 and 25 °C were verysimilar and all spores were able to germinate at 10 °C.Spores of A. ruta-muraria differed in that germination was slowerat 15-25 °C and very much delayed, or even inhibited, at10 °C. Both laboratory and field cultures of A. trichomanesand A. scolopendrium produced male, female and bisexual gametophyteswhereas those of A. ruta-muraria produced only males and bisexuals.The ecological significance of these differences is discussed.Copyright1994, 1999 Academic Press Fern, Asplenium ruta-muraria, Asplenium trichomanes, Asplenium scolopendrium, Phyllitis scolopendrium, spore germination, gametophyte, reproductive biology, temperature effects, field experiments 相似文献
12.
A method is described to determine germination by blue-light excited red fluorescence in the positively photoblastic spores of Dryopteris paleacea Sw. This fluorescence is due to chlorophyll as evidenced from 1) a fluorescence-emission spectrum in vivo, where a bright fluorescence around 675 nm is obtained only in red light (R)-irradiated spores and 2) in vitro measurements with acetone extracts prepared from homogenized spores. Significant amounts of chlorophyll can be found only in R-treated spores; this chlorophyll exhibits an emission band around 668 nm, when irradiated with 430 nm light at 21°C.
Compared to other criteria for germination, such as swelling of the cell, coat splitting, greening, and rhizoid formation, which require longer periods after induction for their expression, chlorophyll fluorescence can be used to quantify germination after two days. This result is confirmed by fluence-response curves for R-induced spore germination; the same relationship between applied R and germination is obtained by the evaluation with the epifluorescence method 2 days after the light treatment as compared with the evaluation with bright-field microscopy 5 days after the inducing R.
Using this technique we show for the first time that Ca2+ contributes to the signaltransduction chain in phytochrome-mediated chlorophyll synthesis in spores of Dryopteris paleacea . 相似文献
Compared to other criteria for germination, such as swelling of the cell, coat splitting, greening, and rhizoid formation, which require longer periods after induction for their expression, chlorophyll fluorescence can be used to quantify germination after two days. This result is confirmed by fluence-response curves for R-induced spore germination; the same relationship between applied R and germination is obtained by the evaluation with the epifluorescence method 2 days after the light treatment as compared with the evaluation with bright-field microscopy 5 days after the inducing R.
Using this technique we show for the first time that Ca
13.
Airborne fungal spores are known carriers of allergen. Correlations between spore counts and allergen concentrations are poor. It is known that germination increases allergen release, implicating spore viability as a determinant of allergen release. During aerial dispersal, spores can be exposed to prolonged periods of ultraviolet (UV) light which can reduce viability of spores. We examined the relation between spore viability and allergen release in two experiments: firstly spores from culture were treated with a UV wavelength of 254?nm (not present in sunlight reaching the earth's surface) or autoclaved, and secondly, spores were exposed to simulated sunlight over three days. In both studies viability was measured (by germination on agar and by metabolic activity with nitro-blue tetrazolium vital stain) and allergen release by the Halogen immunoassay. The UV light reduced the proportion of spores able to germinate but did not affect metabolic activity or allergen release. Autoclaving reduced the proportion of spores releasing allergen by half (p<0.0001). Three days' exposure to simulated sunlight correlated negatively with spore germination and metabolic activity (p<0.0001), but did not affect allergen release (p=0.799). In conclusion, simulated sunlight reduced the metabolic activity and germinability of spores however the proportion releasing allergen remained unaffected. These findings suggest that spore counts may reflect allergen concentrations in the air if spores are dead or dormant. The contribution of viable spores to concentrations of airborne allergen, as well as the role of germination in allergen delivery to the respiratory tract, remains to be resolved. 相似文献
14.
Irradiation of spores of the fern Mohria caffrorum Sw. witheither red light (67.4 µW cm2) or far-red light(63.2 µW cm2) for a period of 24 h induced maximumlevels of germination. Brief irradiations with blue light (127.6µW cm2) administered before or after photoinductioncompletely nullified the effects of red or far-red light; however,with prolonged exposure to blue light, germination levels roseto near maximum. The similar effects of red and far-red lightin promoting spore germination makes the involvement of phytochromein this process questionable. Based on energy requirements,the promotive and inhibitory phases of blue light appear toinvolve independent modes of action. Mohria caffrorum, ferns, spore germination, photoinduction, phytochrome 相似文献
15.
The effects of light on spore germination (protrusion of protonemata)in the liverwort Marchantia polymorpha L. were examined. Sporegermination was found to be light dependent and light irradiationfor 10 h or longer was necessary. Test using specific wavelengthsshowed that the entire spectrum from near UV to red light waseffective, red light being the most effective. Spore germinationcould be induced by intermittent irradiation with 15-min redlight pulses given every 1 or 2 h for 24 h. The effect of intermittentred light was not reversed by subsequent or simultaneous far-redlight irradiation. However, spore germination was inhibitedby the photosynthesis inhibitor DCMU (100 µM). Completeinhibition of spore germination was found when DCMU was givenduring the light period. When DCMU was applied during the darkperiods, only a slight reduction of germination rate was observed.Further, it was found that Chl formed in the spores during imbibitionin darkness. Light sensitivity increased at nearly the samerate as the appearance of Chl. Moreover, spore germination wasinduced in total darkness by the addition of glucose to themedium. These results clearly indicate that photosynthesis mediatesthe photoinduction of spore germination in Marchantia polymorpha. (Received May 13, 1999; Accepted July 14, 1999) 相似文献
16.
MORTON A. G.; DICKERSON A. G. F.; ENGLAND D. J. F. 《Journal of experimental botany》1960,11(1):116-128
The intracellular proteinase enzymes of Penicillium griseofulvumand other fungi increase to levels several times higher thanthat in growing mycelium in the first few hours of nitrogenstarvation, and remain at the higher level unless more assimilablenitrogen is supplied. The rise in proteinase does not take placein absence of oxygen or in the presence of p-fluorophenylalanine,and is not accompanied by net protein breakdown in the myceliumunless synthetic processes are inhibited by lack of oxygen orexogenous carbohydrate. The proteinase activity changes during the life cycle of thefungus, being absent in the spores, very low in the early stagesof germination, and tending to rise steadily during growth.In some conditions the induction of sporulation is associatedwith a rise in proteinase, but there is no simple relation betweenthe two processes. The results are considered to support theview that intracellular proteinase plays a part in protein turnoverin the fungal cell. 相似文献
17.
Dilute colchicine solutions have been found to modify the earlystages of germination of spores in the ferns Dryopteris subpubescensand Goniopteris prolifera. When subsequently grown on soil theprothalli continued to grow abnormally and produced abnormalsperms. Certain prothalli in both species produced large sperms,possibly being diploid, and others and less normal ones producedgiant possibly tetraploid sperms. Monstrous sperms were noted in which two, three, or four bodieswere all united in front, or more rarely where the body forksinto two heads. 相似文献
18.
Photomorphogenesis in Pteris vittata IV. Action spectra for inhibition of phytochrome-dependent spore germination 总被引:1,自引:0,他引:1
Action spectra between 350 and 500 nm for the inhibition ofphytochrome-dependent spore germination in the fern Pteris vittatawere obtained. Both action spectra obtained before and afterred light irradiation have peaks at about 440 nm and 380 nmand shoulders from 440 to 480 nm. These results suggest thatthe phytochrome system is not involved in the inhibitory processof spore germination induced by short irradiation with bluelight. (Received October 8, 1970; ) 相似文献
19.
Jintao Liang Pengfei Zhang Peter Setlow Yong-Qing Li 《Applied and environmental microbiology》2014,80(15):4606-4615
High-precision measurements of size changes of individual bacterial spores based on ellipse fitting to bright-field images recorded with a digital camera were employed to monitor the germination of Bacillus spores with a precision of ∼5 nm. To characterize the germination of individual spores, we recorded bright-field and phase-contrast images and found that the timing of changes in their normalized intensities coincided, so the bright-field images can be used to characterize spore size and refractility changes during germination. The major conclusions from this work were as follows. (i) The sizes of germinating B. cereus spores were nearly unchanged until Trelease, the time of the completion of CaDPA (a 1:1 chelate of Ca2+ and dipicolinic acid [DPA]) release after addition of nutrient germinants. (ii) The minor axis of germinating B. cereus spores rapidly increased by ∼50 nm in a few seconds right after Trelease, while the major axis was slightly decreased or unchanged. Both the minor and major axes remained unchanged for a further 30 to 45 s and then increased by 100 to 200 nm by Tlys, the time of completion of cortex lysis. (iii) Individual spores in a population showed significant heterogeneity in the timing of germination events, such as Trelease and Tlys, but also variation in size changes during germination. (iv) Bacillus subtilis wild-type spores, B. subtilis spores lacking the cortex-lytic enzyme CwlJ, and wild-type Bacillus megaterium spores showed similar kinetics of size changes during nutrient germination. The size increases in germinating spores probably result from uptake of water and cortex lysis after completion of CaDPA release. 相似文献
20.
The stimulation of the germination of Agaricus bisporus sporesby mycelium of the same species has been shown to be due toa volatile metabolite, diffusing into the culture medium andinto the atmosphere. A wide range of other fungi has been foundto affect A. bisporus spores in a similar manner. There wasno evidence . that the stimulant was carbon dioxide. A seven-carbonolefin, isolated from air, which had been passed through culturesof A. bisporus mycelium and dried with phosphorus pentoxide,showed germination-stimulating activity but may have been producedby the action of this drying agent on some other metabolitefrom the mycelium. Volatile materials reported by other workersfrom A. bisporus mycelium and from Saccharomyces cereviseaewere tested and, of these, iso-valeric acid and iso-amyl alcoholwere found to stimulate spore germination of A. bisporus 相似文献