Stromal low temperature compartment derived from the inner membrane of the chloroplast envelope.

Leaf discs of four dicotyledonous species, when incubated at temperatures of 4 to 18 degrees C (optimum at 12 degrees C) for 30 or 60 minutes, responded by accumulations of membranes in the chloroplast stroma in the space between the inner membrane of the envelope and the thylakoids. The accumulated membranes, here referred to as the low temperature compartment, were frequently continuous with the envelope membrane and exhibited kinetics of formation consistent with a derivation from the envelope. Results were similar for expanding leaves of garden pea (Pisum sativum), soybean (Glycine max), spinach (Spinacia oleracea), and tobacco (Nicotiana tabacum). We suggest that the stromal low temperature compartment may be analogous to the compartment induced to form between the transitional endoplasmic reticulum and the Golgi apparatus at low temperatures. The findings provide evidence for the possibility of a vesicular transfer of membrane constituents between the inner membrane of the chloroplast envelope and the thylakoids of mature chloroplasts in expanding leaves.

[1]  P. Weisbeek,et al.  The role of the transit peptide in the routing of precursors toward different chloroplast compartments , 1986, Cell.

[2]  R. Douce Site of Biosynthesis of Galactolipids in Spinach Chloroplasts , 1974, Science.

[3]  E. Heinz,et al.  Lipid Labelling in Intact Chloroplasts from Exogenous Nucleotide Precursors , 1981 .

[4]  J. Joyard,et al.  Structure and Function of the Plastid Envelope , 1980 .

[5]  J. Hoober The Molecular Basis of Chloroplast Development , 1987 .

[6]  J. Harwood Plant Acyl Lipids: Structure, Distribution, and Analysis , 1980 .

[7]  John H. Luft,et al.  IMPROVEMENTS IN EPOXY RESIN EMBEDDING METHODS , 1961, The Journal of biophysical and biochemical cytology.

[8]  J. Kartenbeck,et al.  Membrane flow and intercoversions among endomembranes. , 1979, Biochimica et biophysica acta.

[9]  J. Helsper,et al.  Characterization of galactosyltransferases in spinach chloroplast envelopes , 1987 .

[10]  K. Keegstra,et al.  Galactosyltransferases involved in galactolipid biosynthesis are located in the outer membrane of pea chloroplast envelopes. , 1983, Plant physiology.

[11]  J. Tooze,et al.  Site of addition of N-acetyl-galactosamine to the E1 glycoprotein of mouse hepatitis virus-A59 , 1988, The Journal of cell biology.

[12]  M. Block,et al.  Preparation and characterization of membrane fractions enriched in outer and inner envelope membranes from spinach chloroplasts. II. Biochemical characterization. , 1983, The Journal of biological chemistry.

[13]  E. Heinz,et al.  Biosynthesis of digalactosyldiacylglycerol in plastids from 16:3 and 18:3 plants. , 1990, Plant physiology.

[14]  A. Loud A METHOD FOR THE QUANTITATIVE ESTIMATION OF CYTOPLASMIC STRUCTURES , 1962, The Journal of cell biology.

[15]  D. Morré,et al.  Identification of the 16°C compartment of the endoplasmic reticulum in rat liver and cultured hamster kidney cells , 1989, Biology of the Cell.

[16]  K. Keegstra Transport and routing of proteins into chloroplasts , 1989, Cell.

[17]  D. Lagunoff,et al.  TEMPERATURE DEPENDENCE OF MAST CELL HISTAMINE SECRETION , 1974, The Journal of cell biology.

[18]  E. Heinz,et al.  Distribution of radioactive lipids between envelopes and thylakoids from chloroplasts labelled in vivo. , 1980, European journal of biochemistry.

[19]  M. Farquhar Progress in unraveling pathways of Golgi traffic. , 1985, Annual review of cell biology.

[20]  A. Tartakoff Temperature and energy dependence of secretory protein transport in the exocrine pancreas. , 1986, The EMBO journal.

[21]  E. Fries,et al.  The effects of low temperatures on intracellular transport of newly synthesized albumin and haptoglobin in rat hepatocytes. , 1986, The Biochemical journal.