» Articles » PMID: 16664909

Uptake and Processing of the Precursor to the Small Subunit of Ribulose 1,5-bisphosphate Carboxylase by Leucoplasts from the Endosperm of Developing Castor Oil Seeds

Overview
Journal Plant Physiol
Specialty Physiology
Date 1986 Jul 1
PMID 16664909
Citations 18
Authors
Affiliations
Soon will be listed here.
Abstract

Intact leucoplasts from the endosperm of developing castor oil seed were isolated by Percoll density gradient centrifugation. The precursor to the small subunit of ribulose 1,5-bisphosphate carboxylase from pea was synthesized in vitro from hybrid-selected mRNA. Leucoplasts imported this precursor by an ATP-requiring mechanism similar to that described in chloroplasts (AR Grossman et al. 1980 Nature 285: 625-628). The small subunit precursor was processed to a molecular weight that was identical with that of the mature pea small subunit. These results show that leucoplasts, though specialized for fatty acid biosynthesis and not photosynthesis, have a mechanism of protein import similar to that of chloroplasts.

Citing Articles

Developmental regulation of protein import into plastids.

Chu C, Li H Photosynth Res. 2018; 138(3):327-334.

PMID: 29943361 DOI: 10.1007/s11120-018-0546-4.


Transport of proteins into chloroplasts.

Lubben T, Theg S, Keegstra K Photosynth Res. 2014; 17(1-2):173-94.

PMID: 24429668 DOI: 10.1007/BF00047688.


Recent developments in chloroplast protein transport.

Mishkind M, Scioli S Photosynth Res. 2014; 19(1-2):153-84.

PMID: 24425372 DOI: 10.1007/BF00114573.


A pentapeptide motif related to a pigment binding site in the major light-harvesting protein of photosystem II, LHCII, governs substrate-dependent plastid import of NADPH:protochlorophyllide oxidoreductase A.

Reinbothe C, Pollmann S, Phetsarath-Faure P, Quigley F, Weisbeek P, Reinbothe S Plant Physiol. 2008; 148(2):694-703.

PMID: 18441218 PMC: 2556810. DOI: 10.1104/pp.108.120113.


Malate- and pyruvate-dependent Fatty Acid synthesis in leucoplasts from developing castor endosperm.

Smith R, Gauthier D, Dennis D, Turpin D Plant Physiol. 1992; 98(4):1233-8.

PMID: 16668781 PMC: 1080338. DOI: 10.1104/pp.98.4.1233.


References
1.
Ellis R . Chloroplast protein synthesis: principles and problems. Subcell Biochem. 1983; 9:237-61. DOI: 10.1007/978-1-4613-3533-7_2. View

2.
Laemmli U . Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970; 227(5259):680-5. DOI: 10.1038/227680a0. View

3.
Bradford M . A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976; 72:248-54. DOI: 10.1016/0003-2697(76)90527-3. View

4.
Fish L, Jagendorf A . High rates of protein synthesis by isolated chloroplasts. Plant Physiol. 1982; 70(4):1107-14. PMC: 1065834. DOI: 10.1104/pp.70.4.1107. View

5.
Bonner W, Laskey R . A film detection method for tritium-labelled proteins and nucleic acids in polyacrylamide gels. Eur J Biochem. 1974; 46(1):83-8. DOI: 10.1111/j.1432-1033.1974.tb03599.x. View