scholarly journals EARLY STAGES IN THE DEVELOPMENT OF PLASTID FINE STRUCTURE IN RED AND FAR-RED LIGHT

1964 ◽  
Vol 22 (2) ◽  
pp. 433-442 ◽  
Author(s):  
Shimon Klein ◽  
G. Bryan ◽  
Lawrence Bogorad

Developmental changes in fine structure were studied in plastids of etiolated bean leaves during the time required for the protochlorophyllide-chlorophyllide transformation and the following lag phase prior to chlorophyll accumulation. In agreement with some other workers, two distinct stages of change in the fine structure of proplastids were found to occur upon illumination during this period. The first involves a dissociation of the previously fused units in the prolamellar bodies of the proplastids and occurs simultaneously with the protochlorophyllide-chlorophyllide conversion in light of 655 mµ, but not of 682, 700, or 730 mµ. The effect of the red light could not be reversed by a simultaneously supplied stronger far-red irradiation. The energy requirements for these structural changes parallel those for the pigment conversion. During the following step the vesicles which arose from the fused units of the prolamellar body were dispersed in rows through the stroma, and the prolamellar bodies themselves disappeared. For these changes to occur, higher light energies were required and the leaves had to be illuminated for longer periods. A red preillumination seemed to accelerate the development somewhat. The structural changes could be induced by light of 655 mµ, but also, to a lesser degree, of 730 mµ. No measurable additional chlorophyll accumulated during this period. Thus, the structural changes observed were independent of major changes in pigment content.

1964 ◽  
Vol 22 (2) ◽  
pp. 443-451 ◽  
Author(s):  
Shimon Klein ◽  
Lawrence Bogorad

Etiolated bean leaves supplied δ-amino-levulinic acid in the dark synthesize large amounts of protochlorophyllide which is not converted to chlorophyllide upon illumination of the leaves. The fine structure of the proplastids is not affected by the treatment. When leaves containing "inactive" protochlorophyllide are exposed to light of 700 ft-c for 3 hours, they lose practically all their green pigments. During this period large stacks of closed membrane structures are built up in the region of the prolamellar body. These lamellar structures remain even when no or only traces of pigment are left in the leaves. In untreated control leaves the pigment content remained constant during similar illumination and the structural changes in the plastids consisted of a rearrangement of the vesicles from the prolamellar bodies into strands dispersed through the stroma; lamellae and grana formation occurred later.


1971 ◽  
Vol 8 (1) ◽  
pp. 185-200
Author(s):  
D. R. BERRY ◽  
H. SMITH

The etioplasts of fully dark-grown barley leaves exhibit a relatively low frequency of crystalline prolamellar bodies (ca. 16-20%). Brief red-light treatment leads to rapid disruption of all prolamellar bodies followed by a slow reformation in the subsequent dark period. When several red-light treatments are given with intervening 3-h dark periods, a marked increase in the proportion of crystalline prolamellar bodies is seen. It is suggested that this phenomenon may be associated with the regeneration of protochlorophyll. Red-light pretreatment stimulates the formation of granal thylakoids upon subsequent transfer to continuous white light. This response is correlated with the phytochrome-mediated shortening of the lag phase in chlorophyll-synthesis under identical conditions. Regular arrays of hexagonal tubules 16-19 nm in diameter have been observed often in close juxtaposition to the newly forming thylakoid membranes. These may be aggregations of Fraction I protein, although their exact nature and function is at present Unknown.


1961 ◽  
Vol 11 (2) ◽  
pp. 433-440 ◽  
Author(s):  
Shimon Klein ◽  
A. Poljakoff-Mayber

Proplastids containing a prolamellar body were isolated from leaves of etiolated bean plants. The isolation methods do not necessarily lead to destruction of their submicroscopic structure and most of the isolated proplastids show well preserved outer membranes, lamellar strands, and the prolamellar body. Morphological intactness of the proplastids varies; certain leaf fractions contain single prolamellar bodies as well as proplastids. Since pellets after centrifugation between 350 g and 1000 to 3000 g contain intact proplastids and, as was shown by quantitative experiments, the same fractions show photoconversion of protochlorophyll to chlorophyll, it is supposed that the isolated particles probably retain many of the properties which are characteristic of them in situ. Isolated proplastids may thus be a valuable tool in investigations on the development of the photosynthetic apparatus.


1975 ◽  
Vol 53 (21) ◽  
pp. 2405-2410 ◽  
Author(s):  
Hugh Frick

The 10- to 12-h lag phase in chlorophyll accumulation preceding the rapid accumulation phase in Lemna minor de-etiolating in the light was eliminated by a red light preillumination given about the length of the lag period before the onset of continuous red light. Neither the rate after the lag nor the extent of cholorophyll accumulation differed between preilluminated and control plants. Both the rate of accumulation in controls and the absolute stimulation by preillumination were shown to depend upon the length of time the etiolated plants had been grown in darkness up to 93 days. Only one photoproduct of preillumination contributed to the elimination of the chlorophyll lag phase, but the effect of red light was only partially (about 60%) nullified by subsequent far-red light.


1969 ◽  
Vol 5 (3) ◽  
pp. 757-793
Author(s):  
K. W. HENNINGSEN ◽  
J. E. BOYNTON

Barley seedlings developing at 23 °C in darkness have been studied at various ages for changes in fresh weight, height of shoot, protochlorophyll content and structure of the etioplasts in the primary leaf. Changes of the pigments in vivo, such as the spectral shift of the newly formed chlorophyll and the resynthesis of protochlorophyll, were studied spectrophotometrically prior to and following a 1-min illumination. Concomitantly, leaf tissue was fixed with glutaraldehyde-OsO4 and later analysed in thin sections using the electron microscope. In darkness, protochlorophyll content in the primary leaf, size of the etioplasts, size of the crystalline prolamellar bodies and area of the primary lamellar layers reach their maximum values on the 7th day. Thereafter all the aforementioned parameters decrease, particularly the protochlorophyll content. The structural changes of the prolamellar-body material, rate of the spectral shift of the newly formed chlorophyll and rate of the resynthesis of protochlorophyll in darkness after photoconversion of the original protochlorophyll depend on seedling age. In both 5- and 7-day-old seedlings with high protochlorophyll content, the illumination causes a rapid transformation of the prolamellar bodies. Subsequently in 5-day-old seedlings, a rapid resynthesis of protochlorophyll takes place and the prolamellar bodies recrystallize before dispersal is completed. In the 7-day-old seedlings, resynthesis of protochlorophyll is slower and the prolamellar bodies are largely dispersed into primary lamellar layers before resynthesis of protochlorophyll and reformation of crystalline prolamellar bodies ensue. In 5-day-old seedlings, in which resynthesis of protochlorophyll and recrystallization of the prolamellar bodies are completed within less than 1 h in darkness following illumination, a second illumination effects a more rapid transformation and dispersal of the prolamellar bodies than is observed after the first illumination. In 9- and 11-day-old seedlings, in which the content of protochlorophyll is low, transformation of the prolamellar bodies occurs slowly in darkness following the initial illumination and is not completed within 60 min. No significant protochlorophyll resynthesis and no dispersal of the prolamellar bodies were observed during this time interval. Dispersal of the prolamellar bodies results in an increase in the area of the primary lamellar layers. During reformation of protochlorophyll, a decrease in area of the primary lamellar layers is correlated with an increase in volume and number of the prolamellar bodies. These quantitative relationships between the parameters for prolamellar bodies and primary lamellar layers indicate that, for dispersal and recrystallization of the prolamellar bodies, no significant amount of membrane synthesis is required. Different configurations of the prolamellar bodies can occur: protochlorophyll is associated with the crystalline configurations where the spacing of the tubules is either narrow or wide; chlorophyll is associated with the transformed prolamellar-body configuration. The narrow and wide crystalline configurations appear to be interconvertible, and re-organization does not necessarily involve the primary lamellar layers as an intermediate step. Wide spacing of the tubules coincides with the highest pigment content.


1974 ◽  
Vol 15 (1) ◽  
pp. 31-55
Author(s):  
K. W. HENNINGSEN ◽  
J. E. BOYNTON

The development of plastid membranes was studied in relation to chlorophyll accumulation in dark-grown barley seedlings of various ages after transfer to light. Quantitative electron microscopy showed that the prolamellar body membranes are reorganized into primary lamellar layers which contain sufficient membranes to support grana formation during 24 h of greening. Structural reorganization of the plastid membranes is completed rapidly in young seedlings, but is slow in older seedlings. Chlorophyll accumulates rapidly in young leaves after a short lag. In older leaves there is a longer lag phase before the onset of chlorophyll synthesis, and the final rate of synthesis is lower. Shortly after transferring to light, the crystalline prolamellar bodies in the etioplasts are transformed and then dispersed into lamellar layers with numerous perforations and protuberances. Before the phase of rapid chlorophyll synthesis, many small-diameter 2-disk grana are formed. When chlorophyll begins to accumulate, the perforations are rapidly eliminated from the lamellar layers and a maximum number of 2-disk grana are formed. As greening proceeds additional disks are added to these original 2-disk grana. During the phase of rapid chlorophyll synthesis, pairing of the lamellae is positively correlated with the accumulation of chlorophyll. During greening less chlorophyll appears to be incorporated into the paired regions of the lamellae in young leaves as compared to old leaves. The results on the structural aspects of plastid development are discussed in relation to the formation of photosynthetic capacity.


2021 ◽  
Vol 68 (5) ◽  
pp. 867-872
Author(s):  
M. S. Khristin ◽  
T. N. Smolova ◽  
V. D. Kreslavski

Abstract The dynamics of changes in the photochemical activity of photosystem II (PSII) and low-temperature spectra at 77 K in the first leaves of 11-day winter wheat plants Triticum aestivum L., as well as structural changes in chlorophyll-protein complexes (CPC) of thylakoid membranes during recovery after a short-term (20 min) heating at a temperature of 42°C, were studied. Changes in the Fv/Fm, F735/F695, and F735/F685 ratios indicate inhibition of PSII immediately after heating. Using nondenaturing electrophoresis, it was shown that the light-harvesting Chl a/b complex of PSII does not aggregate immediately after heating but after several hours, after 6 h the desagregation of CPC was observed, which was consistent with an increase in the Fv/Fm ratio upon recovery. The influence of temperature, intensity, and quality of light (white, blue, and red light) on the recovery of PSII activity and low-temperature fluorescence spectra was studied. It was concluded that the recovery is a photo-activated low-energy process, independent of photosynthesis, and the most effective in blue light.


2019 ◽  
Author(s):  
Elin Claesson ◽  
Weixiao Yuan Wahlgren ◽  
Heikki Takala ◽  
Suraj Pandey ◽  
Leticia Castillon ◽  
...  

Phytochrome proteins control the growth, reproduction, and photosynthesis of plants, fungi, and bacteria. Light is detected by a bilin cofactor, but it remains elusive how this leads to activation of the protein through structural changes. We present serial femtosecond X-ray crystallographic data of the chromophore-binding domains of a bacterial phytochrome at delay times of 1 ps and 10 ps after photoexcitation. The structures reveal a twist of the D-ring, which lead to partial detachment of the chromophore from the protein. Unexpectedly, the conserved so-called pyrrole water is photodissociated from the chromophore, concomitant with movement of the A-ring and a key signalling aspartate. The changes are wired together by ultrafast backbone and water movements around the chromophore, channeling them into signal transduction towards the output domains. We suggest that the water dissociation is key to the phytochrome photoresponse, explaining the earliest steps of how plants, fungi and bacteria sense red light.


CONVERSAZIONES were held this year on 9 May and 27 June. At the first conversazione twenty-seven exhibits and two films were shown. The fine structure of plant roots in relation to transport of nutrient ions and water was demonstrated by Dr D. T. Clarkson of the A.R.C. Letcombe Laboratory, Wantage and Dr A. W. Robards of the Department of Biology, University of York. Two major pathways by which nutrients and water move radially across the cortex towards the central vascular tissue have been distinguished by the use of tracer studies of adsorption by different zones of intact root systems, microautoradiography and electron microscopy. Movement can be apoplastic through cell walls, or symplastic between cells joined by plasmodesmata. As the root ages, structural changes in the endodermis reduce movement in the former pathway but the symplast is not interrupted by the elaboration of endodermal walls because plasmodesmatal connexions remain intact. These observations help explain the contrasting extent to which different ions and water reach the shoot from young and mature parts of root systems.


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