These authors contributed equally to this work.
SUMMARYDespite significant progress in clarifying the subunit compositions and functions of the multiple NADPH dehydrogenase (NDH-1) complexes in cyanobacteria, the subunit maturation and assembly of their NDH-1 complexes are poorly understood. By transformation of wild-type cells with a transposon-tagged library, we isolated three mutants of Synechocystis sp. PCC 6803 defective in NDH-1-mediated cyclic electron transfer and unable to grow under high light conditions. All the mutants were tagged in the same slr1097 gene, encoding an unknown protein that shares significant homology with the Arabidopsis protein chlororespiratory reduction 6 (CRR6). The slr1097 product was localized in the cytoplasm and was required for efficient assembly of NDH-1 complexes. Analysis of the interaction of Slr1097 with 18 subunits of NDH-1 complexes using a yeast two-hybrid system indicated a strong interaction with NdhI but not with other Ndh subunits. Absence of Slr1097 resulted in a significant decrease of NdhI in the cytoplasm, but not of other Ndh subunits including NdhH, NdhK and NdhM; the decrease was more evident in the cytoplasm than in the thylakoid membranes. In the Δslr1097 mutant, NdhH, NdhI, NdhK and NdhM were hardly detectable in the NDH-1M complex, whereas almost half the wild-type levels of these subunits were present in NDH-1L complex; similar results were observed in the NdhI-less mutant. These results suggest that Slr1097 is involved in the maturation of NdhI, and that assembly of the NDH-1M complex is strongly dependent on this factor. Maturation of NdhI appears not to be crucial to assembly of the NDH-1L complex.
Based upon highly selective and irreversible Hg2+‐promoted deprotection of the dithioacetal reaction, a new water‐soluble “turn‐on” fluorescent chemosensor (1) was prepared and exhibited high selectivity and sensitivity towards the Hg2+ ion over other heavy and transition‐metal ions in pure water by transforming a weakly fluorescent precursor (colorless) to a highly fluorescent aldehyde (yellow–green; see figure) with a 155‐fold increase in fluorescent intensity.
A series of new fluorescent chemosensors 5a–5e, composed of two aminonaphthalimide fluorophores and 2,6‐bis((N‐aminoalkyl)aminocarboxy)pyridines, were prepared, characterized, and their fluorescent properties towards heavy and transition metal (HTM) ions were investigated. Chemosensors 5c–5e exhibited high selectivity and sensitivity for Cu2+ ion over other HTM ions with fluorescent quenching (green to colourless). It clearly demonstrated that the length of the linkers (diamines) between the aminonaphthalimides and 2,6‐dicarboxypyridine of 5a–5e was very important for their sensitivity and selectivity for Cu2+ ion over other HTM ions.
Acute respiratory distress syndrome (ARDS) is a common critical illness in respiratory care units with a huge public health burden. Despite tremendous advances in the prevention and treatment of ARDS, it remains the main cause of intensive care unit (ICU) management, and the mortality rate of ARDS remains unacceptably high. The poor performance of ARDS is closely related to its heterogeneous clinical syndrome caused by complicated pathophysiology. Based on the different pathophysiology phases, drugs, protective mechanical ventilation, conservative fluid therapy, and other treatment have been developed to serve as the ARDS therapeutic methods. In recent years, there has been a rapid development in nanomedicine, in which nanoparticles as drug delivery vehicles have been extensively studied in the treatment of ARDS. This study provides an overview of pharmacologic therapies for ARDS, including conventional drugs, natural medicine therapy, and nanomedicine. Particularly, we discuss the unique mechanism and strength of nanomedicine which may provide great promises in treating ARDS in the future.
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