Plastid and seedling development in SAN-9789 [4-chloro-5-(methylamine)-2-(α,α,α-trifluoro-m-tolyl)-3-(2H)-pyridasinone]-treated etiolated bean seedlings

1980 ◽  
Vol 58 (1) ◽  
pp. 25-35 ◽  
Author(s):  
Anthony D. Pardo ◽  
Jerome A. Schiff

SAN 9789[4-chloro-5-(methylamine)-2-(α,α,α-trifluoro-m-tolyl)-3-(2H)-pyridasinone] inhibits carotenoid synthesis at the level of phytoene in Phaseolus vulgaris L. Although carotenoids are greatly reduced in the primary leaves, prolamellar bodies and thylakoid membranes are formed containing phototransformable protochlorophyll(ide). SAN 9789 also produces developmental effects similar to those of red light since seedlings treated in darkness are short, show plumular unhooking, formation of adventitious roots, expansion of primary leaves and full expansion of the first trifoliate leaf and first internode. The effect is not directly on phytochrome since far red light does not reverse the effect of SAN. If abscisic acid (ABA) is indeed formed from carotenoids, we may be observing the consequences of reduced levels of ABA leading to reduced ethylene production as occurs with red light. The first trifoliate leaf of SAN-treated plants contains practically no carotenoids (0.2%) compared with untreated 7-day-old, etiolated primary leaves yet shows normal development of etioplasts, prolamellar bodies, thylakoid membranes, and phototransformable protochlorophyll(ide). In Euglena, lack of carotenoids stops synthesis and assembly of other membrane components; in higher plants this type of regulation does not appear to operate.

1976 ◽  
Vol 54 (15) ◽  
pp. 1819-1826 ◽  
Author(s):  
Hugh Frick ◽  
Raymond F. Jones

During the 12-h lag period in chlorophyll accumulation after the onset of white-light illumination of Lemna minor etiolated for 35 days, a rapid increase in visible fronds per culture occurred. This new frond production then assumed a log-linear rate of increase, and total protein per unit fresh weight came to parallel the rate of increase in fresh weight per plant. The ribosomal RNA content of 45-day-etiolated plants was deficient in 23S and 16S species compared with green plants. The prolamellar bodies of etioplasts were either tightly or loosely paracrystalline within the same cell; they were without extended perforate lamellae, which developed during far-red-light illumination even while prolamellar bodies persisted. The development of chloroplasts in deetiolating L. minor was typical of other higher plants. The developmental sequence in green Lemna included proplastid to deeply stacked granal chloroplast within several millimetres. Plastid profiles suggestive of division configurations occurred only in primordial cells of green and etiolated plants. The relatively small numbers of plastids in any given stage of differentiation may account for the sensitivity of plastid development to inhibitors of protein and nucleic acid synthesis.


2018 ◽  
Author(s):  
Sapana Nongmaithem ◽  
Sameera Devulapalli ◽  
Yellamaraju Sreelakshmi ◽  
Rameshwar Sharma

One sentence summaryN-1-naphthylphthalamic acid (NPA) treatment stimulates tomato hypocotyl elongation likely by elevating ethylene emission and lowering indole-3-butyric acid levels in the seedlings.AbstractIn higher plants, phytohormone indole-3-acetic acid is characteristically transported from the apex towards the base of the plant, termed as polar auxin transport (PAT). Among the inhibitors blocking PAT, N-1-naphthylphthalamic acid (NPA) that targets ABCB transporters is most commonly used. NPA-treated light-grown Arabidopsis seedlings show severe inhibition of hypocotyl and root elongation. In light-grown tomato seedlings, NPA inhibited root growth, but contrary to Arabidopsis stimulated hypocotyl elongation. The NPA-stimulation of hypocotyl elongation was milder in blue, red, and far-red light-grown seedlings. The NPA-treatment stimulated emission of ethylene from the seedlings. The scrubbing of ethylene by mercuric perchlorate reduced NPA-stimulated hypocotyl elongation. NPA action on hypocotyl elongation was antagonized by 1-methylcyclopropene, an inhibitor of ethylene action. NPA-treated seedlings had reduced levels of indole-3-butyric acid and higher levels of zeatin in the shoots. NPA did not alter indole-3-acetic levels in shoots. The analysis of metabolic networks indicated that NPA-treatment induced moderate shifts in the networks compared to exogenous ethylene that induced a drastic shift in metabolic networks. Our results indicate that in addition to ethylene, NPA-stimulated hypocotyl elongation in tomato may also involve zeatin and indole-3-butyric acid. Our results indicate that NPA-mediated physiological responses may vary in a species-specific fashion.


Crop Science ◽  
1977 ◽  
Vol 17 (5) ◽  
pp. 797-799 ◽  
Author(s):  
Paul J. Kretchmer ◽  
J. L. Ozbun ◽  
Stuart L. Kaplan ◽  
D. R. Laing ◽  
D. H. Wallace

1973 ◽  
Vol 19 (7) ◽  
pp. 831-836 ◽  
Author(s):  
Martin Kessel ◽  
Robert MacColl ◽  
Donald S. Berns ◽  
Mercedes R. Edwards

The particulate material (intact and dissociated phycobilisomes), adjacent to the thylakoids of Plectonema boryanum and Calothrix parietina, was examined in thin sections and in freshly prepared C-phycocyanin extracts. For the latter a method was developed using spheroplasts of log-phase cells. When examined by sedimentation velocity centrifugation, the sedimentation coefficients of the rapidly extracted C-phycocyanin were found to be 18 S and 5 S. Also, a 10-S boundary was observed with P. boryanum. When C. parietina was grown under red light the 18-S aggregates increased to 20 S. The 18 S particles, in electron micrographs of negatively stained preparations, displayed eight subunits surrounding a central one. The possibility that some subunits fall out of the plane of view is contemplated in proposing a dodecamer arrangement for such particles. The 20-S particles were also examined by electron microscopy. However, the precise number of monomer units associated with either the 18-S or 20-S particles has not yet been ascertained. Thin sections of intact algal cells are presented to demonstrate the presence of phycobilisomes along the outer faces of the thylakoid membranes.


Planta ◽  
2016 ◽  
Vol 245 (4) ◽  
pp. 793-806 ◽  
Author(s):  
Reimund Goss ◽  
Anne Greifenhagen ◽  
Juliane Bergner ◽  
Daniela Volke ◽  
Ralf Hoffmann ◽  
...  

2019 ◽  
Vol 116 (35) ◽  
pp. 17316-17322 ◽  
Author(s):  
Orly Levitan ◽  
Muyuan Chen ◽  
Xuyuan Kuang ◽  
Kuan Yu Cheong ◽  
Jennifer Jiang ◽  
...  

A descendant of the red algal lineage, diatoms are unicellular eukaryotic algae characterized by thylakoid membranes that lack the spatial differentiation of stroma and grana stacks found in green algae and higher plants. While the photophysiology of diatoms has been studied extensively, very little is known about the spatial organization of the multimeric photosynthetic protein complexes within their thylakoid membranes. Here, using cryo-electron tomography, proteomics, and biophysical analyses, we elucidate the macromolecular composition, architecture, and spatial distribution of photosystem II complexes in diatom thylakoid membranes. Structural analyses reveal 2 distinct photosystem II populations: loose clusters of complexes associated with antenna proteins and compact 2D crystalline arrays of dimeric cores. Biophysical measurements reveal only 1 photosystem II functional absorption cross section, suggesting that only the former population is photosynthetically active. The tomographic data indicate that the arrays of photosystem II cores are physically separated from those associated with antenna proteins. We hypothesize that the islands of photosystem cores are repair stations, where photodamaged proteins can be replaced. Our results strongly imply convergent evolution between the red and the green photosynthetic lineages toward spatial segregation of dynamic, functional microdomains of photosystem II supercomplexes.


1960 ◽  
Vol 43 (4) ◽  
pp. 841-851 ◽  
Author(s):  
Ludwig Bergmann

The cultivation of single cells of Nicotiana tabacum L. var. "Samsun" and Phaseolus vulgaris L. var. "Early Golden Cluster" on a thin agar layer in Petri dishes is described. Under these conditions about 20 per cent of the cells divided repeatedly and established tissue clones which could be isolated and maintained as growing tissue cultures. It was possible also to follow the successive divisions of isolated cells and to observe their behavior during cytogenesis under the microscope.


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