» Articles » PMID: 5427113

In Vitro Protein Synthesis by Plastids of Phaseolus Vulgaris. IV. Amino Acid Incorporation by Etioplasts and Effect of Illumination of Leaves on Incorporation by Plastids

Overview
Journal Plant Physiol
Specialty Physiology
Date 1970 Apr 1
PMID 5427113
Citations 12
Authors
Affiliations
Soon will be listed here.
Abstract

Protein synthesis in vitro by etioplasts and chloroplasts from Phaseolus vulgaris was examined to study the factors regulating the development of etioplasts into chloroplasts. The properties of incorporation of (14)C-leucine into protein by etioplasts from plants grown 6.5 days in darkness are similar to those of chloroplasts from plants of the same age that were illuminated for 12 hours. However, the rate of incorporation per plastid by chloroplasts is 4 times higher than the rate of amino acid incorporation by etioplasts. When 6-day-old plants are placed in light, this 4-fold increase occurs within 6 hours and is maintained up to 36 hours. The difference in rate of amino acid incorporation into protein between etioplasts and chloroplasts represents a real difference in the ability of etioplasts and chloroplasts to synthesize protein. A difference in pool size of leucine between etioplasts and chloroplasts does not account for the difference in amino acid incorporation between etioplasts and chloroplasts. Also the difference in photosynthetic capabilities of etioplasts and chloroplasts does not account for the difference in the ability to incorporate amino acid into protein. Furthermore, there are no factors in homogenates of etiolated leaves which inactivate amino acid incorporation into protein by chloroplasts. The difference in rates of amino acid incorporation between etioplasts and chloroplasts is correlated with the state of development of the plastids. The plastids have increased ability to incorporate amino acid into protein when the plastids are undergoing growth and differentiation.

Citing Articles

Changes in envelope permeability during chloroplast development.

Hampp R, Schmidt H Planta. 2014; 129(1):69-73.

PMID: 24430818 DOI: 10.1007/BF00390916.


Protein synthesis by isolated chloroplasts.

Gnanam A, Subbaiah C, Mannan R Photosynth Res. 2014; 19(1-2):129-52.

PMID: 24425371 DOI: 10.1007/BF00114572.


Chloroplast Protein Synthesis in the Chromophytic Alga Olisthodiscus luteus: Cell Cycle Analysis.

Reith M, Cattolico R Plant Physiol. 1985; 79(1):231-6.

PMID: 16664376 PMC: 1074857. DOI: 10.1104/pp.79.1.231.


Kinetics of Membrane Transport during Chloroplast Development.

Hampp R Plant Physiol. 1978; 62(5):735-40.

PMID: 16660596 PMC: 1092211. DOI: 10.1104/pp.62.5.735.


Changes in Enzyme Regulation during Growth of Maize: III. Intracellular Localization of Homoserine Dehydrogenase in Chloroplasts.

Bryan J, Lissik E, Matthews B Plant Physiol. 1977; 59(4):673-9.

PMID: 16659916 PMC: 542471. DOI: 10.1104/pp.59.4.673.


References
1.
Hoober J, Siekevitz P, Palade G . Formation of chloroplast membranes in Chlamydomonas reinhardi y-1. Effects of inhibitors of protein synthesis. J Biol Chem. 1969; 244(10):2621-31. View

2.
Jacobson A . A procedure for isolation of proplastids from etiolated maize leaves. J Cell Biol. 1968; 38(1):238-44. PMC: 2107456. DOI: 10.1083/jcb.38.1.238. View

3.
Kupke D . Correlation of a soluble leaf protein with chlorophyll accumulation. J Biol Chem. 1962; 237:3287-91. View

4.
Jacobson A, Swift H, Bogorad L . Cytochemical studies concerning the occurrence and distribution of RNA in plastids of Zea mays. J Cell Biol. 1963; 17:557-70. PMC: 2106211. DOI: 10.1083/jcb.17.3.557. View

5.
Spencer D, Wildman S . THE INCORPORATION OF AMINO ACIDS INTO PROTEIN BY CELL-FREE EXTRACTS FROM TOBACCO LEAVES. Biochemistry. 1964; 3:954-9. DOI: 10.1021/bi00895a019. View