Walfield A M, Hershberger C L
J Bacteriol. 1978 Mar;133(3):1437-43. doi: 10.1128/jb.133.3.1437-1443.1978.
The mechanism for the turnover-synthesis of chloroplast DNA in the absence of net synthesis during the chloroplast maturation in Euglena gracilis was determined. DNA synthesis was measured by incorporation of32Pi into chloroplast DNA. The density label, 15N, was incorporated to examine the mechanism of turnover-synthesis. The newly synthesized segments represent a replacement of segments in the DNA containing 1.5 X 10(3) to 6.1 X 10(3) nucleotides. Twenty-three fragments of chloroplast DNA, generated by digestion with the restriction endonuclease EcoRI, became labeled with 32Pi. Turnover-synthesis, therefore, replaces segments throughout the molecule of chloroplast DNA.
确定了纤细裸藻叶绿体成熟过程中在无净合成情况下叶绿体DNA周转合成的机制。通过将³²Pi掺入叶绿体DNA来测量DNA合成。加入密度标记物¹⁵N以研究周转合成的机制。新合成的片段代表了含有1.5×10³至6.1×10³个核苷酸的DNA片段的替换。用限制性内切酶EcoRI消化产生的23个叶绿体DNA片段被³²Pi标记。因此,周转合成替换了叶绿体DNA分子中的各个片段。