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Base excision repair (BER) is the main pathway protecting cells from the continuous damage to DNA inflicted by reactive oxygen species. BER is initiated by DNA glycosylases, each of which repairs a particular class of base damage. NTHL1, a bifunctional DNA glycosylase, possesses both glycolytic and ß-lytic activities with a preference for oxidized pyrimidine substrates. Defects in human NTLH1 drive a class of polyposis colorectal cancer. We report the first X-ray crystal structure of hNTHL1, revealing an open conformation not previously observed in the bacterial orthologs. In this conformation, the six-helical barrel domain comprising the helix-hairpin-helix (HhH) DNA binding motif is tipped away from the iron sulphur cluster-containing domain, requiring a conformational change to assemble a catalytic site upon DNA binding. We found that the flexibility of hNTHL1 and its ability to adopt an open configuration can be attributed to an interdomain linker. Swapping the human linker sequence for that of Escherichia coli yielded a protein chimera that crystallized in a closed conformation and had a lower binding affinity for lesion-containing DNA. This large scale interdomain rearrangement during catalysis is unprecedented for a HhH superfamily DNA glycosylase and provides important insight into the molecular mechanism of hNTHL1.

The bacterial flagellar motor, a remarkable rotary machine, can rapidly switch between counterclockwise (CCW) and clockwise (CW) rotational directions to control the migration behavior of the bacterial cell. The flagellar motor consists of a bi-directional spinning rotor surrounded by torque-generating stator units. Recent high-resolution in vitro and in situ structural studies have revealed stunning details of the individual components of the flagellar motor and their interactions in both the CCW and CW senses. In this review, we discuss these structures and their implications for understanding the molecular mechanisms underlying flagellar rotation and switching.

Chlorella pyrenoidosa is a microalga that holds enormous potential as a source of renewable energy. Nuclear radiation is commonly used to modify natural microalgal phenotypes to enhance specified functions. However, the mechanisms underlying such modifications are poorly understood. Here, we use a multidisciplinary approach to analyze wild-type Chlorella pyrenoidosa and a nuclear-irradiated mutant known for its higher growth rate and photosynthetic efficiency. A combination of focused ion beam scanning electron microscopy (FIB-SEM), cryo-FIB milling, and cryo-electron tomography (cryo-ET) achieve visualization of the microalgae and their organelles in unprecedented detail. Compared to the wild-type cell, the nuclear-irradiated mutant and its subcellular organelles, including the chloroplast, significantly increase in volume by 1.2-fold. Moreover, proteomics and metabolomics data indicate rubisco overexpression by 1.07-fold in the mutant, consistent with enhancement of carbon fixation in photosynthesis and the observed enlargement of subcellular morphology. Furthermore, cryo-ET reveals enlarged membrane width in the thylakoid of the mutant, suggesting an upregulation role for chlorophyll synthesis and chloroplast construction. Collectively, our studies reveal the detailed architectures of C. pyrenoidosa wild-type and a mutant with higher growth rate and photosynthetic efficiency, providing a basis for understanding how subcellular organelles function collaboratively to support macroscopic traits.