Light-induced absorbance changes in the fungus Verticillium agaricinum

Light-induced absorbance changes were investigated in vivo in the fungus Verticillium agaricinum (Link) Corda. There was a broad light-induced absorbance decrease in the blue and near UV with a maximum at 384 nm. An action spectrum indicated that the absorbance changes were due to photo-bleaching of a pigment with an absorption spectrum that was similar to the action spectrum. Neither redox reactions nor energy metabolism were involved in the photo-bleaching process. A direct comparison of action spectra for light-induced absorbance changes and photo-induction of carotenogenesis suggests that the photo-bleaching may not be related to photo-induction of carotenogenesis.     

Perithecial Formation in Gelasinospora reticulispora VII: Action Spectra in UV Region for the Photoinduction and the Photoinhibition of Photoinductive Effect Brought by Blue Light

An action spectrum for photoinduction of perithecial formationafter a prior 72 h dark growth period was determined in theUV region with apically growing mycelia of a sordariaceous fungus,Gelasinospora reticulispora. The spectrum exhibited a peak at280 nm. Quantum effectiveness of 280 nm irradiation was ca.1.7 times higher than that of 450 nm light. The number of peritheciainduced by UV radiation was saturated at a lower level as comparedwith blue light. UV radiation having a fluence greater thanthe saturation level decreased the number of induced perithecia.UV radiation that was given after a saturating exposure to inductiveblue light inhibited the inductive effect of blue light. Anaction spectrum for this inhibition exhibited a peak between260 and 270 nm. Monochromatic light beyond 350 nm had no inhibitoryeffect. Inhibitory effects of UV radiation given after inductiveblue light irradiation were observed in the fluence range wherephotoinductive effects of UV radiation became obvious. Therefore,the true height of the UV peak in the photoinduction actionspectrum,when free of distortion from the inhibitory effect, should behigher than the peak obtained in this study. (Received August 20, 1983; Accepted November 4, 1983)     

Sporulatim in the fungus Verticillium agaricinum: Reversal of blue light inhibition by Ultraviolet radiation

In colonies ranging from 3- to 5-days-old, light in general stimulates conidiation in Verticillium , including V. agaricinum and several strains of V. albo-atrum . However, when growth was started by inoculating with conidial suspension spread evenly over the plate, it was found that blue light inhibited conidiation in our strain of V. egaticinum . We most light-sensitive phase was around 9 h after inoculation. A broad band blue light pulse of 10 J m⁻² saturated the response. The inhibitory effect of blue light could be reversed by a subsequent ultraviolet (UV) radiation, but a further effect of blue light was lost after the UV pulse. Blue light inhibition was also prevented by IJV radiation administered before the blue light.     

Effect of light and phosphate on conidiation in the fungus Verticillium agaricinum

Verticillium agaricinum (Link) Corda, grown in a yeast extract-sucrose medium, conidiated abundantly in darkness after irradiation with near ultraviolet (290–400 nm) for 15 min or blue light (400–550 nm) for 60 min. Few conidia were formed in total darkness. Exposure to 30 min of near ultraviolet light suppressed conidiation. Conidiation was also suppressed by phosphate in excess of 10⁻⁴ M irrespective of light condition. After irradiation with near ultraviolet light for more than 30 min, there was a cessation of growth and a change in colony color from yellow to reddish. The color does not appear to be due to a carotenoid because the colonies turned from red to yellow when covered with acid. At pH lower than 6.0 the pigment has an absorption maximum around 390 nm, whereas at higher pH it is around 540 nm. Thus, it appears that irradiation of V. agaricinum with near ultraviolet may cause an increase in pH, which in turn produces the change of colony color from yellow to reddish.     

Effects of light flashes on the dark closure of Albizzia julibrissin pinnules

An electronic flash unit is used to deliver, at the beginning of a 10 min dark period and within a few ms, large doses of light to Albizzia julibrissin pinnules, to ascertain their effects on the rate of pinnule closing. In a series of alternating light flashes at 710 and 550 nm, the first 710 nm light flash significantly retards closing. A following light flash at 550 nm negates the far-red induced delay. The second 710 nm light flash delays closing less effectively than the first when given within 4 s after the green flash, but is just as effective when given after 30 s. The delay brought about by the second 710 nm light flash is again abolished by a light flash at 550 nm. A light flash at 660 nm has no effect on pinnule closing by itself and is also ineffective in reversing the far-red induced delay. A series of ten 710 nm light flashes becomes most effective in delaying closure when there is a dark interval of one min between flashes. The closing delay induced by a 710 nm light flash escapes reversal by a 550 nm light flash when the dark interval between the two flashes exceeds 2–3 min. A 750 nm light flash has no retarding effect on pinnule closing, but it becomes effective when preceded by a 660 nm or 550 nm light flash. The results obtained are suggested to be due to light absorbed by phytochrome and an unknown photoreceptor with green, far-red photoreversal property.     

UV‐A/BLUE LIGHT–INDUCED REACTIVATION OF SPORE GERMINATION IN UV‐B IRRADIATED ULVA PERTUSA (CHLOROPHYTA)1

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.     

Regulation of the xanthophyll cycle pool size in duckweed (Lemna minor) plants

Duckweed ( Lemna minor L.) plants grown under high light are characterized, when compared to low light acclimated plants, by a higher xanthophyll cycle (VAZ) pool content, but also by a higher proportion of photoconvertible violaxanthin and a superior ability to synthesize VAZ pigments. When duckweed plants were transferred to a high light environment a general response was the quick adjustment of the carotenoid composition, mainly xanthophyll cycle pigments. These changes resulted from a balance between a process of continuous light-independent carotenoid degradation and a light-induced accumulation. The use of norflurazon, an inhibitor of carotenogenesis, allowed us to demonstrate that the observed light induced increase of the VAZ pool was mainly caused by de novo synthesis through carotenogenesis. The extent of light-induced carotenogenesis was proportional to the light treatment and also to the operation of the VAZ cycle since it was partly abolished by treatments leading to a low activity of the VAZ cycle, such as low light, DTT or DCMU. These results suggest that not only the light itself, but also a mechanism triggered by a factor associated with the de-epoxidation state of the VAZ cycle controls carotenogenesis at some point before phytoene formation in the terpenoid biosynthesis pathway.     

Studies on the near-UV effect on carotenogenesis in Verticillium agaricinum

Carotenoids identified in Verticillium agaricinum under near-UV were beta-, zeta-, and gamma-carotenes, neurosporene, torulene, neurosporaxanthin and one of its esters. Evidence supports the proposal that gamma-carotene, and not torulene, is the immediate precursor of neurosporaxanthin. It is also suggested that phytochrome may be involved in the high irradiance reactions (HIR) causing carotenoid synthesis in this fungus although there is no knowledge of how this is effected. Spores grown under near-UV conditions varied in size and shape from those grown in the dark. A new pigment (390, 420 nm) is also proposed as the photoreceptor for carotenogenesis in V. agaricinum.     

Light emitting diode(LED)‐based trapping of the greenhouse whitefly (Trialeurodes vaporariorum)

Visual traps like yellow sticky card traps are used for monitoring and control of the greenhouse whitefly (Trialeurodes vaporariorum). However, reflected intensity (brightness) and hence, attractiveness depend on the ambient light conditions, and the colour (wavelength) might not fit with the sensitivity of whitefly photoreceptors. The use of light emitting diodes (LEDs) is a promising approach to increase the attractiveness, specificity and adaptability of visual traps. We constructed LED‐based visual traps equipped with blue and green high‐power LEDs and ultraviolet (UV) standard LEDs according to the putative spectral sensitivities of the insects' photoreceptors. In a series of small‐scale choice and no‐choice recapture experiments, the factors time of day as well as light intensity and light quality (colour) of LED traps were studied in terms of attractiveness compared to yellow traps without LEDs. Green LED traps (517 nm peak wavelength) were comparably attractive in no‐choice experiments but clearly preferred over yellow traps in all choice experiments. The time of day had a clear effect on the flight activity of the whiteflies and thereby on the trapping success. Blue LEDs (474 nm) suppressed the attractiveness of the light traps when combined with green LEDs suggesting that a yet undetected photoreceptor, sensitive for blue light, and an inhibiting interaction with the green receptor, might exist in T. vaporariorum. In choice experiments between LED traps emitting green light only or in combination with UV (368 nm), the green‐UV combination was preferred. In no‐choice night‐time experiments, UV LEDs considerably increased whitefly flight activity and efficacy of trapping. Most likely, the reason for the modifying effect of UV is the stimulating influence on flight activity. In conclusion, it seems that the use of green LEDs alone or in combination with UV LEDs could be an innovative option for improving attractiveness of visual traps.     

Photoinduced Carotenogenesis in Chlorotic Euglena gracilis

Light induces β-carotene synthesis in streptomycin-bleached Euglena gracilis Z. Light-adapted, chemostat-grown cells have up to 10-fold as much β-carotene and 25% more protein than similarly grown, dark-adapted cells. Carotenogenesis does not occur under anaerobic conditions or in the presence of diphenylamine, cyanide, or cycloheximide. The blue portion of the spectrum (360-560 nm) is most active in initiating carotenogenesis. The level of cellular carotenoids is influenced by the type of carbon source and to some degree by pH. Phytofluence and ζ-carotene are present in dark-grown cells but not in cells grown aerobically in white light (360-1120 nm). These pigments, however, were present in cells grown in yellow or green light (above 486 nm) or in cells exposed to white light anaerobically. The carotenoids are localized in two types of structures at the light microscope level. A protoporphyrin was isolated from Euglena, and its role as a possible photoreceptor during carotenogenesis is suggested.     

Far-red induced changes of the protochlorophyllide components in wheat leaves

Biosynthesis of chlorophyll is partly controlled by the phytochrome system. In order to study the effects of an activated phytochrome system on the protochlorophyllide (PChlide) biosynthesis without accompanying phototransformation to chlorophyll, wheat seedlings (Triticum aestivum L. cv. Starke II Weibull) were irradiated with long wavelength far-red light of low intensity. Absorption spectra were measured in vivo after different times in the far-red light or in darkness. The relationship between the different PChlide forms, the absorbance ratio _{650nm636 nm} changed with age in darkness, and the change was more pronounced when the leaves were grown in far-red light. Absorption spectra of dark-grown leaves always showed a maximum in the red region at 650 nm. For leaves grown in far-red light the absorption at 636 nm was high, with a maximum at the 5 day stage where it exceeded the absorption at 650 nm. At the same time there was a maximum in the total amount of PChlide accumulated in the leaves, about 30% more than in leaves grown in darkness. But the amount of the directly phototransformable PChlide, mainly PChlide_650–657, was not increased. The amount of PChlide_628–632, or more probably the amount of (PChlide_628–632, + PChlide _636–657) was thus higher in young wheat leaves grown in far-red light than in those grown in darkness. After the 5 day stage the absorption at 636 nm relative to 650 nm decreased with age, and at the 8 day stage the spectra were almost the same in both types of leaves. Low temperature fluorescence spectra of the leaves also showed a change in the ratio between the different PChlide forms. The height of the fluorescence peak at 632 nm relative to the peak at 657 nm was higher in leaves grown in far-red light than in dark-grown leaves. – After exposure of the leaves to a light flash, the half time for the Shibata shift was measured. It increased with age both for leaves grown in darkness and in far-red light; but in older leaves grown in far-red light (7–8 days) the half time was slightly longer than in dark-grown leaves. – The chlorophyll accumulation in white light as well as the leaf unrolling were faster for leaves pre-irradiated with far-red light. The total length of the seedlings was equal or somewhat shorter in far-red light, but the length of the coleoptile was markedly reduced from 8.1 ± 0.1 cm for dark-grown seedlings to 5.2 ± 0.1 cm for seedlings grown in far-red light.     

Action spectra for polarotropism and phototropism in protonemata of the fern Adiantum capillus-veneris

The action spectrum for polarotropism was determined, using the Okazaki large spectrograph, by brief irradiation with light between 260 nm and 850 nm in single-celled protonemata of the fern Adiantum capillus-veneris L., which had been cultured for 6 days in red light and then in the dark for 15 h. The action spectrum had a peak at around 680 nm. This effect was nullified by subsequent irradiaton with far-red light, and typical red/far-red reversibility was observed, indicating the involvement of phytochrome. Polarized ultraviolet or blue light had no effect on the direction of apical growth. The action spectrum for phototropism was also determined in the red light region by means of brief microbeam irradiation of a flank of the subapical region of the protonema. This spectrum showed a peak at 662 nm which was consistent with the absorption peak of phytochrome, but not with the peak of the action spectrum for polarotropism.     

不同光质补光对促早栽培‘瑞都香玉’葡萄果实品质的影响

以4年生‘贝达’嫁接的早熟葡萄品种‘瑞都香玉’为试材,研究设施促早栽培条件下,紫外光、蓝光和红蓝光不同光质补光对果实品质的影响,结果表明: 促早栽培节能日光温室内环境属于典型的弱蓝紫光和弱紫外光环境.与对照(未补光)相比,夜间6 h的蓝光和紫外光补光处理可显著加快葡萄果实发育过程中质量和果粒纵横径的增大、果实糖含量的升高以及酸含量的下降,红蓝光效果不明显.果实成熟期紫外光补光处理果实的单粒质量最高,蓝光与红蓝光处理显著高于对照;蓝光补光处理果实葡萄糖、果糖和总糖含量最高,紫外光次之,红蓝光略高于对照.与对照相比,蓝光补光处理可显著加快果实中里那醇、α-萜品醇、橙花醇等萜烯类组分含量高峰的出现,而紫外光、红蓝光补光处理差异较小.果实成熟期蓝光补光处理果实中里那醇、香茅醇等萜烯类物质含量最高,紫外光补光处理里那醇含量较高,香叶醇、己醛、E-2-己烯醛等主要香气物质的含量最高,而红蓝光补光处理里那醇的含量与对照相比有所降低.紫外光、蓝光和红蓝光3种光质补光处理均增加了果实中醛酮类物质的种类及含量.表明蓝光补光处理果实发育最快,成熟最早,糖含量最高,里那醇等萜烯类物质含量高峰出现的时间最早;紫外光补光处理果实的单粒质量最大,主要萜烯类组分含量高;红蓝光补光处理对改善果实品质的效果不明显.     

Wing colors of Chrysozephyrus butterflies (Lepidoptera; Lycaenidae): ultraviolet reflection by males

Wing colors of the four species of Chrysozephyrus butterflies were analyzed by a spectrophotometer. As the dorsal wing surface of males showed a strong reflectance when the specimen was tilted, measurements were made by the tilting method. The dorsal wing surface of males which appears green to the human eye reflected UV (315-350 nm) as well as green light (530-550 nm). The reflectance rate of UV to visible green light varied among species with a higher rate for C. hisamatsusanus and C. ataxus, and a lower rate for C. smaragdinus and C. brillantinus. The peak wavelength and the peak height did not shift when the specimen was exposed to direct sunlight at least for 16 hr. Artificial removal of scales by scratching the wing surface decreased reflectance. Blue marks on the forewings of C. brillantinus, C. hisamatsusanus and C. ataxus females reflected UV to visible light of short wavelength, and orange marks on the dorsal surface of the forewing and the ventral surface of the hindwing of C. samaragdinus females showed a higher reflectance at longer wavelengths.     

Are two photoreceptors involved in the flowering of a long-day plant?

The effect of daylength extension with narrow spectral bands on the flowering of a long-day plant, Brassica campestris L. cv. Ceres, was investigated to obtain clues to the identity of the photoreceptor involved. Extension of a 9 h photoperiod with 5 h of light pulses at various wavelengths resulted in maximal flowering occurring after irradiation at 710 nm, less at 730 nm, and none at 550, 660 and 750 nm. Flowering at 710 and 730 nm was negated by simultaneous exposures at 550 nm, but not at 660 nm. A short preirradiation at 660 nm enabled a following irradiation at 750 nm to induce flowering. This latter induction was prevented by 550 nm irradiation.
Short flashes of light at 710 nm induced flowering that was negated by a following flash at 550 nm but not at 660 nm. The negation by 550 nm radiation was prevented by subsequent flashes at 710 nm, indicating photoreversibility. A flash at 660 nm enabled subsequent light flashes at 750 nm to initiate flowering that was reversed by a following 550 nm flash.
From the results showing the necessity of red and far-red lights, it is proposed that flowering in this long-day plant is due to two photoreceptors - one is phytochrome and the other an unknown pigment with far-red, green photoreversible properties. By using fluence response data, it is deduced that the unidentified photoreceptor has weak absorption bands in the far-red, but has a strong absorption band in the green. Flowering is induced when effects of red light absorbed by phytochrome interact with effects of far-red light absorbed by the unidentified photoreceptor.     

Suppression and reactivation of UV-induced sporulation by blue light inBipolaris oryzae

Sporulation inBipolaris oryzae was induced by UV radiation (295 nm), but the number of conidia gradually decreased with increasing duration of UV radiation longer than 1 min. The inductive effect of UV radiation can be nullified by blue light (459 nm) applied immediately before or after inductive UV radiation shorter than 1 min. In contrast, the number of conidia increased with an increasing duration of blue light applied after inductive UV radiation longer than 1 min, but not if it was applied before UV radiation. The present study firstly revealed the possibility of photoreactivation inB. oryzae sporulation.     

Blue Light Inhibits Mitosis in Tissue Culture Cells

Irradiation of the mitotic (prophase and prometaphase) tissue culture PK (pig kidney embryo) cells using mercury arc lamp and band-pass filters postponed or inhibited anaphase onset. The biological responses observed after irradiation were: (i) normal cell division, (ii) delay in metaphase and then normal anaphase and incomplete cytokinesis, (iii) exit into interphase without separation of chromosomes, (iv) complete mitotic blockage. Cell sensitivity to the light at wavelengths from 423 and 488 nm was nearly the same; to the near UV light (wavelength 360 nm) it was 5–10 times more; to the green light (wavelength >500 nm) it was at least 10 times less. To elucidate the possible mechanism of the action of blue light we measured cell adsorption and examined cell autofluorescence. Autofluorescence of cytoplasmic granules was exited at wavelengths of 450–490 nm, but not at >500 nm. In mitotic cells fluorescent granules accumulated around the spindle. We suppose blue light irradiation induces formation of the free radicals and/or peroxide, and thus perturb the checkpoint system responsible for anaphase onset.     

Blue light regulation of stomata in wheat seedlings. II. Action spectrum and search for action dichroism

The stomatal conductance response to low intensity blue light was studied in wheat seedlings ( Triticum aestivum L. cv. Starke II, Weibull) under red background illumination. Reciprocity was shown to be valid for illumination times from 10 s up to about 2 min. The action spectrum, constructed from fluence rate response curves, showed a maximum peak at 445–450 nm, another peak at 470 nm, a slight shoulder at 420 nm and a plateau between 370–400 nm. The relationship with action spectra for other blue light responses is discussed. The blue light response of wheat stomata did not exhibit action dichroism (the direction of the electrical vector of polarized blue light did not influence the response of the guard cells).     

Mechanism of Photoregulated Carotenogenesis in Rhodotorula minuta VII. Action Spectrum for Photoinduced Carotenogenesis

An action spectrum for photoinduced carotenogenesis in the yeast,Rhodotorula minuta, was determined over the wavelength rangefrom 250 nm to 770 nm. The action spectrum had a prominent peak at about 280 nm, withshoulders at 340, 370 and 400 nm. In addition, at wavelengthsfrom 260 nm to 400 nm, all slopes of fluence-response curveswere approximately equal, and reciprocity was obtained at eachwavelength tested. The action spectrum obtained was different from any action spectrumso far reported for photoinduced carotenogenesis and suggeststhat a new type of chromoprotein plays a major role as a photoreceptor. ³Present address: Koshi Agricultural Extension Office of FukuiPrefecture, Matsumoto, Fukui, 910 Japan (Received March 31, 1989; Accepted December 8, 1989)