Processing of cellulose synthase (AcsAB) from Gluconacetobacter hansenii 23769

Prashanti R. Iyer, Yu An Liu, Ying Deng, John B. McManus, Teh Hui Kao, Ming Tien

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

The cellulose synthase protein (AcsAB) is encoded by a single gene in Gluconacetobacter hansenii ATCC 23769. We have examined the processing pattern of this enzyme and the localization of the cleavage products by heterologously expressing the truncated portions of the AcsAB protein and using specific antibodies generated against these regions. We found that the AcsAB protein is processed into three polypeptide subunits of molecular masses 46 kDa, 34 kDa and 95 kDa. The 46 kDa polypeptide (AcsAcat) harbors the conserved glycosyltransferase domain and hence contains the catalytic subunit of the enzyme. This polypeptide is localized in the cytoplasmic membrane. The 34 kDa polypeptide (AcsAreg) is the regulatory subunit with the cyclic diGMP-binding PilZ domain. This polypeptide is largely cytoplasmic. The 95 kDa subunit (AcsB) is of unknown function and contains a predicted signal peptide at its N-terminus. This subunit is localized in the outer membrane. In addition to this, we have also localized the AcsC protein in the outer membrane, confirming its predicted localization based on the OM-signal sequence at its N-terminus.

Original languageEnglish (US)
Pages (from-to)92-98
Number of pages7
JournalArchives of Biochemistry and Biophysics
Volume529
Issue number2
DOIs
StatePublished - Jan 15 2013

All Science Journal Classification (ASJC) codes

  • Biophysics
  • Biochemistry
  • Molecular Biology

Fingerprint

Dive into the research topics of 'Processing of cellulose synthase (AcsAB) from Gluconacetobacter hansenii 23769'. Together they form a unique fingerprint.

Cite this