ABSTRACT
Light-independent chlorophyll (Chl) biosynthesis is a prerequisite for the assembly of photosynthetic pigment-protein complexes in the dark. Dark-grown Larix decidua Mill. seedlings synthesize Chl only in the early developmental stages and their Chl level rapidly declines during the subsequent development. Our analysis of the key regulatory steps in Chl biosynthesis revealed that etiolation of initially green dark-grown larch cotyledons is connected with decreasing content of glutamyl-tRNA reductase and reduced 5-aminolevulinic acid synthesizing capacity. The level of the Chl precursor protochlorophyllide also declined in the developing larch cotyledons. Although the genes chlL, chlN and chlB encoding subunits of the light-independent protochlorophyllide oxidoreductase were constitutively expressed in the larch seedlings, the accumulation of the ChlB subunit was developmentally regulated and ChlB content decreased in the fully developed cotyledons. The efficiency of chlB RNA-editing was also reduced in the mature dark-grown larch seedlings. In contrast to larch, dark-grown seedlings of Picea abies (L.) Karst. accumulate Chl throughout their whole development and show a different control of ChlB expression. Analysis of the plastid ultrastructure, photosynthetic proteins by Western blotting and photosynthetic parameters by gas exchange and Chl fluorescence measurements provide additional experimental proofs for differences between dark and light Chl biosynthesis in spruce and larch seedlings.
Subject(s)
Chlorophyll/biosynthesis , Picea/metabolism , Pinaceae/metabolism , Seedlings/metabolism , Amino Acid Sequence , Base Sequence , Blotting, Western , Chlorophyll/chemistry , Darkness , Fluorescence , Gene Expression Regulation, Developmental , Gene Expression Regulation, Plant , Light , Light-Harvesting Protein Complexes/genetics , Light-Harvesting Protein Complexes/metabolism , Microscopy, Electron , Photosystem I Protein Complex/genetics , Photosystem I Protein Complex/metabolism , Picea/genetics , Picea/growth & development , Pinaceae/genetics , Pinaceae/growth & development , Plant Proteins/genetics , Plant Proteins/metabolism , Plastids/ultrastructure , Protochlorophyllide/biosynthesis , RNA Editing , Reverse Transcriptase Polymerase Chain Reaction , Seedlings/genetics , Time FactorsABSTRACT
We have found and sequenced a significant part of the previously described tellurite resistance determinant on mini-Mu derivative pPR46, named pNT3B, originally cloned from a large conjugative plasmid pTE53, found in Escherichia coli. This plasmid contains genes essential for tellurite resistance, together with the protective region bearing genes terX, Y, W, and the conserved spacing region bearing several ORFs of unknown function. Computer analysis of obtained sequence revealed a close similarity to the formerly described ter operons found on the Serratia marcescens plasmid R478 and the chromosome of Escherichia coli O157:H7. This finding confirms the presence of a whole region on the large conjugative plasmid that pTE53 originated from a uropathogenic E. coli strain, and suggests its possible role in horizontal gene transfer, resulting in the development of new pathogenic E. coli strains.
