期刊
出版社
NATL ACAD SCIENCES
DOI: 10.1073/pnas.2111745119
关键词
biomineralization; bacterial organelles; magnetosome; magnetotactic bacteria; magnetite
资金
- NIH [R01GM084122, R35GM127114]
This study identifies MamE as a key regulator of magnetosome membrane growth in magnetotactic bacteria. Disruption of MamE's protease activity restricts membrane growth and limits the size of magnetite particles. MamO and MamM, the upstream regulators of MamE protease activity, are also involved in magnetosome membrane growth. Moreover, Mms6 and MamD are identified as two MamE substrates that are related to magnetosome membrane growth and size control.
Magnetosomes are lipid-bound organelles that direct the biomineralization of magnetic nanoparticles in magnetotactic bacteria. Magnetosome membranes are not uniform in size and can grow in a biomineralization-dependent manner. However, the underlying mechanisms of magnetosome membrane growth regulation remain unclear. Using cryoelectron tomography, we systematically examined mutants with defects at various stages of magnetosome formation to identify factors involved in controlling membrane growth. We found that a conserved serine protease, MamE, plays a key role in magnetosome membrane growth regulation. When the protease activity of MamE is disrupted, magnetosome membrane growth is restricted, which, in turn, limits the size of the magnetite particles. Consistent with this finding, the upstream regulators of MamE protease activity, MamO and MamM, are also required for magnetosome membrane growth. We then used a combination of candidate and comparative proteomics approaches to identify Mms6 and MamD as two MamE substrates. Mms6 does not appear to participate in magnetosome membrane growth. However, in the absence of MamD, magnetosome membranes grow to a larger size than the wild type. Furthermore, when the cleavage of MamD by MamE protease is blocked, magnetosome membrane growth and biomineralization are severely inhibited, phenocopying the MamE protease-inactive mutant. We therefore propose that the growth of magnetosome membranes is controlled by a protease-mediated switch through processing of MamD. Overall, our work shows that, like many eukaryotic systems, bacteria control the growth and size of biominerals by manipulating the physical properties of intracellular organelles.
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