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Structure and Organisation of Chloroplast Genome
The chloroplast genomes of vascular plants and most algae are quite similar. In general structure and organization, especially by comparison to the wholesale variation seen in the nuclear and mitochondrial genomes. With one Possible exception, all known chloroplast genomes are circular DNA molecules. Size variation is greatest among green algae in which most chloroplast genomes range between about 85 and 300 kb.

The genome of Acetabularia chloroplasts is exceptional in being very large (approximately 2,000 kb) and perhaps composed of linear rather than circular DNA molecules. However, in angiosperms chloroplast genomes in all but two of over 200 species examined are circular and range in size between 120 and 160 kb. The low end of this range is a single group of legumes which lack one copy of the large (15-25 kb) repeated sequence characteristic of most other chloroplast genomes.

Thus the great majority of angiosperm chloroplast genomes actually fall into the relatively narrow range of 135 and 160 kb. Chloroplast DNA (ctDNA) consists of a circular molecule of 83-128 x 106 molecular weight with a size of 1.21-1.93 x 105 bp, which contains about 85% single copy sequences. DNA is present in about 30-200 copies per chloroplast.

A number of genes have been located on the circle and one of the important features is the presence of two copies of the ribosomal DNA sequences. These sequences are often but not always-present on a large inverted repeat. Other genes mapped include those for the large subunit of RuBP. Case, tRNAs, subunits of ATP synthase, and cytochrome.

Most of this size variation can be accounted for by the presence or absence of a portion of the plastid genome which has been duplicated and is present in an inverted orientation in the plastid DNA molecule. The location of this inverted repeat is relatively fixed with respect to other genes and it separates a small single-copy region from a large single copy DNA region.

In most higher plants the inverted repeat is 22 to 26 kbp, within which the rRNA transcription unit is located. In geranium the repeated DNA is larger and genes such as psbB, petB, pelD, petA and rbcL are included in the inverted repeat. Finally, some plastid genomes, such as those in pea and mung bean, lack inverted repeat.

Plastid gene content in higher plants is very constant and many polycistronic transcription units are conserved. Several gene pairs such as psaA­-psaB, psbD-psbC, atpB-atpE, are contranscribed in all the higher plant plas­tid genomes examined to date. The contranscription of genes may ensure that the synthesis of subunits is stoichiometric and or could promote protein-­protein interactions required for assembly of functional complexes.

For example, psaA and psaB encode polypeptides which are tightly associated in the reaction centre of PSI. Other genes, such as rbcL and some gene encoding tRNAs, are not part of polycistronic transcription units. While the plastid gene content of higher plants is very constant, variation in gene order is evident, which results primarily from DNA inversion. DNA.

Inversions have reshuffled plastid genomes such that distances between genes, and relative orientation of transcription units, vary considerably in genomes of higher plants. For example, rps16 is proximal to trnk in barley, whereas in pea rbcL occupies this position. The greatest variation in gene order is found in peas (at least 12 rearrangements), perhaps due to lack of an inverted repeat in this plasmid genome which might stabilize the genome.