bcsB encodes a single-pass inner-membrane/periplasmic BcsB-family accessory subunit of the bacterial cellulose synthase complex. It associates with the BcsA catalytic subunit and helps organize the periplasmic path for nascent cellulose during c-di-GMP-controlled cellulose biosynthesis.
| GO Term | Evidence | Action | Reason |
|---|---|---|---|
| GO:0005886 plasma membrane | IEA GO_REF:0000120 | ACCEPT | Summary: Plasma membrane is the appropriate bacterial inner-membrane location for BcsB. Reason: UniProt places BcsB in the cell inner membrane as a single-pass membrane protein. Supporting Evidence: file:PSEPK/bcsB/bcsB-uniprot.txt SUBCELLULAR LOCATION: Cell inner membrane file:PSEPK/bcsB/bcsB-goa.tsv GO:0005886 plasma membrane |
| GO:0006011 UDP-alpha-D-glucose metabolic process | IEA GO_REF:0000002 | MODIFY | Summary: UDP-alpha-D-glucose metabolism is an over-broad donor-substrate process for BcsB. Reason: BcsB is a cellulose synthase regulatory subunit in bacterial cellulose biosynthesis; the broad UDP-glucose metabolic-process term should be replaced by the pathway process. Proposed replacements: cellulose biosynthetic process Supporting Evidence: file:PSEPK/bcsB/bcsB-uniprot.txt PATHWAY: Glycan metabolism; bacterial cellulose biosynthesis. file:PSEPK/bcsB/bcsB-goa.tsv GO:0006011 UDP-alpha-D-glucose metabolic process |
| GO:0016020 membrane | IEA GO_REF:0000002 | MODIFY | Summary: Membrane is correct but less specific than the bacterial plasma membrane assignment already present. Reason: BcsB is specifically assigned to the cell inner membrane, so GO:0005886 is the preferred location term. Proposed replacements: plasma membrane Supporting Evidence: file:PSEPK/bcsB/bcsB-uniprot.txt SUBCELLULAR LOCATION: Cell inner membrane file:PSEPK/bcsB/bcsB-goa.tsv GO:0016020 membrane |
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Download this section (compressed HTML)Q: Does KT2440 BcsB directly bind c-di-GMP, or is its regulatory role indirect through BcsA and local c-di-GMP-metabolism partners?
Q: Which local bcs-locus accessory proteins are required for BcsB-dependent cellulose synthesis and export?
Experiment: Reconstitute KT2440 BcsA/BcsB membrane complexes and test whether BcsB variants affect cellulose synthase activity or BcsA PilZ-dependent c-di-GMP activation.
Type: in vitro regulatory and complex-assembly assay
Experiment: Compare cellulose production and biofilm matrix phenotypes in wild-type, bcsB deletion, and bcsB complementation strains.
Type: targeted genetics and biofilm polysaccharide assay
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