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| Content Provider | Springer Nature Link |
|---|---|
| Author | Katada, Hitoshi Sei, Hidetake Mizobe, Yasushi Sumaoka, Jun Komiyama, Makoto |
| Copyright Year | 2007 |
| Abstract | The structures of Ce4+ complexes that are active for DNA hydrolysis were determined for the first time by X-ray crystallography. The crystals were prepared from a 1:2 mixture of Ce(NH4)2(NO3)6 and dipicolinic acid (2,6-pyridinedicarboxylic acid). Depending on the recrystallization conditions, three types of crystals were obtained. Some of the Ce4+ ions in these complexes have enough coordinated water molecules that can directly and indirectly participate in the catalysis. The distances between the Ce4+ and the dipicolinate ligand are considerably shorter than those in the corresponding La3+ and Ce3+ complexes. On the other hand, the distances between the Ce4+ and its coordinated water are similar to those for the La3+ and Ce3+ complexes. In a proposed mechanism of DNA hydrolysis, the scissile phosphodiester linkage is notably activated by coordination to Ce4+ and attacked by the Ce4+-bound hydroxide. The process is further assisted by acid catalysis of Ce4+-bound water. |
| Starting Page | 249 |
| Ending Page | 255 |
| Page Count | 7 |
| File Format | |
| ISSN | 09498257 |
| Journal | JBIC Journal of Biological Inorganic Chemistry |
| Volume Number | 13 |
| Issue Number | 2 |
| e-ISSN | 14321327 |
| Language | English |
| Publisher | Springer-Verlag |
| Publisher Date | 2007-11-07 |
| Publisher Place | Berlin, Heidelberg |
| Access Restriction | One Nation One Subscription (ONOS) |
| Subject Keyword | Cerium DNA cleavage Phosphodiester hydrolysis Crystal structure Microbiology Biochemistry |
| Content Type | Text |
| Resource Type | Article |
| Subject | Biochemistry Inorganic Chemistry |
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