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                <identifier>oai:data.mendeley.com/x3xwc52z86.1</identifier>
                <datestamp>2025-05-22T07:23:30Z</datestamp>
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    <dc:creator>xu, xudong</dc:creator>
    <dc:title>Discovery of two natural strains closely similar to the model strain Anabaena sp. PCC 7120 used in molecular studies of heterocyst differentiation</dc:title>
    <dc:publisher>Mendeley Data</dc:publisher>
    <dc:description>Fig.S1 Comparison of gamma plasmids (a) or delta plasmids (b) from Anabaena strains FACHB-595, FACHB-709 and PCC 7120
Fig.S2 Electrophoretograms of PCR products showing the segregation of mutants. a to k, PCR examination of hetR, hetP, hetZ, patS, patU3, patX, patL, patA, patN, nrrA and hetC mutants
Each mutant was examined with two pairs of primers: the first pair, with one primer located within the deleted region and the other primer outside the deleted region (lanes 1, 3, 5 and 7); the second pair, with both primers outside the deleted region (lanes 2, 4, 6 and 8). Lanes 1-2, the deletion mutant of FACHB-595; lanes 3-4, the wild type of FACHB-595; lanes 5-6, the deletion mutant of FACHB-709; lanes 7-8, the wild type of FACHB-709; M, marker. The Trans 5K marker (0.3, 0.5, 0.8, 1, 1.5, 2, 3, 5 kb) was used in a, d, e, g, i and k, while that used in other electrophoretograms was the 100-bp marker (0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1.0, 1.2, 1.5 kb).
Table S1 List of strains, plasmids and primers used in this study</dc:description>
    <dc:subject>Cyanobacteria</dc:subject>
    <dc:subject>Genome</dc:subject>
    <dc:contributor>Hu, Xi</dc:contributor>
    <dc:contributor>Wang, Weipeng</dc:contributor>
    <dc:type>Dataset</dc:type>
    <dc:identifier>doi:10.17632/x3xwc52z86.1</dc:identifier>
    <dc:identifier>oai:data.mendeley.com/x3xwc52z86.1</dc:identifier>
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    <dc:date>2025-05-22T07:23:30Z</dc:date>
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