Literature DB >> 32989086

Comparison of Single and Multiple Turnovers of SecYEG in Escherichia coli.

Chunfeng Mao1, Priya Bariya1, Yuying Suo1, Linda L Randall2.   

Abstract

Precursor proteins are translocated across the cytoplasmic membrane in Escherichia coli by the general secretory, or Sec, pathway. The main components of the pathway are the integral membrane heterotrimeric SecYEG complex and the peripheral membrane ATPase, SecA. In this study, we have applied an in vitro assay using inverted cytoplasmic membrane vesicles to investigate the complex cycle that leads to translocation. We compared the apparent rate constants for nine precursors under two experimental conditions, single turnover and multiple turnovers. For each precursor, the rate constant for a single turnover was higher than for multiple turnovers, indicating that a different step limits the rate under the two conditions. We conclude that the rate-limiting step for a single turnover is an early step in the initial phase of transit through the channel, whereas the rate of multiple turnovers is limited by the resetting of the translocon. The presence of the chaperone SecB during multiple turnovers increased the maximal amplitude translocated for the three precursor species tested, pGBP, pPhoA, and proOmpA, and also increased the apparent rate constants for both pGBP and pPhoA. The rate constant for proOmpA was decreased by the presence of SecB.IMPORTANCE Vastly different experimental techniques and conditions have been used to study export in E. coli We demonstrated that altering experimental conditions can change the step that is observed during study. Investigators should consider specific experimental conditions when comparing data from different laboratories, as well as when comparing data from different experiments within a laboratory. We have shown that each precursor species has inherent properties that determine the translocation rate; thus generalizations from studies of a single species must be made with caution. A summary of advantages and disadvantages in use of nine precursors is presented.
Copyright © 2020 American Society for Microbiology.

Entities:  

Keywords:  E. coli; SecA; SecYEG; multiple turnovers; protein export; protein translocation; rate-limiting step; secretion; single turnover; translocon

Mesh:

Substances:

Year:  2020        PMID: 32989086      PMCID: PMC7685557          DOI: 10.1128/JB.00462-20

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  38 in total

1.  The PrlA and PrlG phenotypes are caused by a loosened association among the translocase SecYEG subunits.

Authors:  F Duong; W Wickner
Journal:  EMBO J       Date:  1999-06-15       Impact factor: 11.598

Review 2.  The protein-conducting channel SecYEG.

Authors:  Andreas K J Veenendaal; Chris van der Does; Arnold J M Driessen
Journal:  Biochim Biophys Acta       Date:  2004-11-11

3.  Multiple SecA molecules drive protein translocation across a single translocon with SecG inversion.

Authors:  Kazuhiro Morita; Hajime Tokuda; Ken-ichi Nishiyama
Journal:  J Biol Chem       Date:  2011-11-10       Impact factor: 5.157

4.  SecA, the motor of the secretion machine, binds diverse partners on one interactive surface.

Authors:  Dylan B Cooper; Virginia F Smith; Jennine M Crane; Hilary C Roth; Angela A Lilly; Linda L Randall
Journal:  J Mol Biol       Date:  2008-06-24       Impact factor: 5.469

5.  Chaperone SecB from Escherichia coli mediates kinetic partitioning via a dynamic equilibrium with its ligands.

Authors:  T B Topping; L L Randall
Journal:  J Biol Chem       Date:  1997-08-01       Impact factor: 5.157

6.  Coassembly of SecYEG and SecA Fully Restores the Properties of the Native Translocon.

Authors:  Priya Bariya; Linda L Randall
Journal:  J Bacteriol       Date:  2018-12-07       Impact factor: 3.490

7.  Orientation of membrane vesicles from Escherichia coli prepared by different procedures.

Authors:  M Futai
Journal:  J Membr Biol       Date:  1974       Impact factor: 1.843

8.  Identification and characterization of an Escherichia coli gene required for the formation of correctly folded alkaline phosphatase, a periplasmic enzyme.

Authors:  S Kamitani; Y Akiyama; K Ito
Journal:  EMBO J       Date:  1992-01       Impact factor: 11.598

9.  Direct visualization of the E. coli Sec translocase engaging precursor proteins in lipid bilayers.

Authors:  Raghavendar Reddy Sanganna Gari; Kanokporn Chattrakun; Brendan P Marsh; Chunfeng Mao; Nagaraju Chada; Linda L Randall; Gavin M King
Journal:  Sci Adv       Date:  2019-06-12       Impact factor: 14.136

Review 10.  Structure-based working model of SecDF, a proton-driven bacterial protein translocation factor.

Authors:  Tomoya Tsukazaki
Journal:  FEMS Microbiol Lett       Date:  2018-06-01       Impact factor: 2.742

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  3 in total

1.  Refined measurement of SecA-driven protein secretion reveals that translocation is indirectly coupled to ATP turnover.

Authors:  William J Allen; Daniel W Watkins; Mark S Dillingham; Ian Collinson
Journal:  Proc Natl Acad Sci U S A       Date:  2020-11-30       Impact factor: 11.205

2.  Synchronized Real-time Measurement of Sec-mediated Protein Translocation.

Authors:  Riti Gupta; Dmitri Toptygin; Christian M Kaiser
Journal:  Bio Protoc       Date:  2021-08-20

3.  Rate-limiting transport of positively charged arginine residues through the Sec-machinery is integral to the mechanism of protein secretion.

Authors:  William J Allen; Robin A Corey; Daniel W Watkins; A Sofia F Oliveira; Kiel Hards; Gregory M Cook; Ian Collinson
Journal:  Elife       Date:  2022-04-29       Impact factor: 8.713

  3 in total

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