Macromolecular Physiology Of Plastids

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.

2015 ◽  
Vol 42 (3) ◽  
pp. 441-452 ◽  
Author(s):  
J. S. Knypl

Cotyledons dissected from 5-day-old etiolated cucumber seedlings were incubated in solutions on AMO-1618, B-Nine, CCC and Phosfon D for 48 h in light. In some tests the retardants were applied in mixed solutions with GA<sub>3</sub> or BAP. IAA oxidase was extracted and purified by means of molecular sieving through a bed of Sephadex G-25. The retardants inhibited chlorophyll synthesis by 50 % or more, and had essentially no effect on IAA oxidase activity per cotyledon basis. GA<sub>3</sub> and BAP also had no effect on enzyme activity in spite of a fact that the compounds stimulated growth of the cotyledons. The crude enzyme extract from B-Nine treated cotyledons showed lower IAA oxidase activity in comparison with the water treated control, the effect being due to a longer lag-phase preceding the initiation of IAA oxidation. KNO<sub>3</sub> strikingly stimulated expansional growth of the cotyledons, the effect being correlated with the accelerated chlorophyll accumulation. KNO<sub>3</sub> had no effect on IAA oxidase activity per cotyledon and decreased it per gram fr wt. It is concluded that [1] the growth rate of cucumber cotyledons is not correlated with IAA oxidase activity, and ;[2] the growth retarding compounds do not affect IAA oxidase system is this tissue.


1974 ◽  
Vol 1 (1) ◽  
pp. 119 ◽  
Author(s):  
DJ Simpson ◽  
CO Chichester ◽  
TH Lee

The effects of 2-(4-chlorophenylthio)ethyldiethylammonium chloride (CPTA) on chlorophyll accumulation, carotenoid biosynthesis and plastid ultrastructure were examined in expanding excised pumpkin cotyledons. CPTA in the dark caused an increased synthesis of non-photoconvertible protochlorophyll but had no effect on the ultrastructure of the starch-containing plastids. In the light, CPTA was a powerful inhibitor of chlorophyll synthesis in greening cotyledons, especially at high light intensity, and induced the accumulation of lycopene. When applied to the greened cotyledons, CPTA caused the transformation of the chloroplasts to chromoplast-like organelles containing osmiophilic globules and lycopene crystalloids. Two other structurally similar compounds,diethyl[4-{3'-(4"-methylphenyl)-3-oxoprop-2' -enyl}phenoxyethyl]ammonium chloride (SK&F 13831) and (2-chloroethyl)trimethylammonium chloride (chlormequat), also caused lycopene accumulation and inhibited chlorophyll synthesis. It is possible that CPTA can induce the formation of chromoplasts from proplastids and chloroplasts in tissue that does not normally contain such organelles.


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.


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.


1975 ◽  
Vol 2 (4) ◽  
pp. 543 ◽  
Author(s):  
E Newell ◽  
KG Rienits

A spontaneous non-lethal chlorophyll mutant of hexaploid wheat was shown to have a greatly diminished rate of chlorophyll accumulation compared to the wild type when 8-day-old dark-grown plants were illuminated with white light. The rate of conversion of protochlorophyllide to chlorophyll was approximately the same in both types. When leaves from dark-grown plants were incubated in �-aminolaevulinate, protoporphyrin and protochlorophyll accumulated in the mutant whereas larger amounts of protochlorophyll accumulated in the wild type. It was concluded that the mutation brings about a restriction in the rate of conversion of protoporphyrin to magnesium protoporphyrin and its methyl ester. The effect of the mutation on protoporphyrin and protochlorophyll accumu- lation was intensified in crosses of the mutant with lines deficient in one of the No. 7 chromosomes, which control chlorophyll synthesis.


2015 ◽  
Vol 42 (3) ◽  
pp. 431-439 ◽  
Author(s):  
J. S. Knypl

Cotyledons were excised from 5-day old etiolated cucumber seedlings and .grown for 24 or 48 h in solutions of plant growth retardants: AMO-1618,B-Nine, CCC and phosfon D, supplemented with KNO<sub>3</sub> (10<sup>-2</sup>M) in light. Nitrate reductase (NR) activity was determined <i>in vivo</i>. CCC and Phosfon D at high concentrations had no effect on nitrate reductase activity in 24 h tests. CCC at 5xl0<sup>-2</sup> M enhanced NR activity in longer 48 h tests; Phosfon D was inhibitory in that case. AMO-1618 markedly decreased NR activity. B-Nine strikingly enhanced NR activity in KNO<sub>3</sub> induced cytoledons; the effect was positively correlated with the concentration of B-Nine. Ali the compounds inhibited chlorophyll synthesis.


2010 ◽  
Vol 52 (9) ◽  
pp. 809-816 ◽  
Author(s):  
Ming Yuan ◽  
Mo-Yun Xu ◽  
Shu Yuan ◽  
Yang-Er Chen ◽  
Jun-Bo Du ◽  
...  

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.


1966 ◽  
Vol 41 (10) ◽  
pp. 1695-1700 ◽  
Author(s):  
Peter M. Shugarman ◽  
David Appleman

eLife ◽  
2020 ◽  
Vol 9 ◽  
Author(s):  
Christopher I Cazzonelli ◽  
Xin Hou ◽  
Yagiz Alagoz ◽  
John Rivers ◽  
Namraj Dhami ◽  
...  

Carotenoids are a core plastid component and yet their regulatory function during plastid biogenesis remains enigmatic. A unique carotenoid biosynthesis mutant, carotenoid chloroplast regulation 2 (ccr2), that has no prolamellar body (PLB) and normal PROTOCHLOROPHYLLIDE OXIDOREDUCTASE (POR) levels, was used to demonstrate a regulatory function for carotenoids and their derivatives under varied dark-light regimes. A forward genetics approach revealed how an epistatic interaction between a ζ-carotene isomerase mutant (ziso-155) and ccr2 blocked the biosynthesis of specific cis-carotenes and restored PLB formation in etioplasts. We attributed this to a novel apocarotenoid retrograde signal, as chemical inhibition of carotenoid cleavage dioxygenase activity restored PLB formation in ccr2 etioplasts during skotomorphogenesis. The apocarotenoid acted in parallel to the repressor of photomorphogenesis, DEETIOLATED1 (DET1), to transcriptionally regulate PROTOCHLOROPHYLLIDE OXIDOREDUCTASE (POR), PHYTOCHROME INTERACTING FACTOR3 (PIF3) and ELONGATED HYPOCOTYL5 (HY5). The unknown apocarotenoid signal restored POR protein levels and PLB formation in det1, thereby controlling plastid development.


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