Literature DB >> 11389694

Overproduction, purification and novel redox properties of the dihaem cytochrome c, NapB, from Haemophilus influenzae.

A Brigé1, J A Cole, W R Hagen, Y Guisez, J J Van Beeumen.   

Abstract

The napB gene of the pathogenic bacterium Haemophilus influenzae encodes a dihaem cytochrome c, the small subunit of a heterodimeric periplasmic nitrate reductase similar to those found in other bacteria. In order to obtain sufficient protein for biophysical studies, we aimed to overproduce the recombinant dihaem protein in Escherichia coli. Initial expression experiments indicated that the NapB signal peptide was not cleaved by the leader peptidase of the host organism. Apocytochrome was formed under aerobic, semi-aerobic and anaerobic growth conditions in either Luria--Bertani or minimal salts medium. The highest amounts of apo-NapB were produced in the latter medium, and the bulk was inserted into the cytoplasmic membrane. The two haem groups were covalently attached to the pre-apocytochrome only under anaerobic growth conditions, and with 2.5 mM nitrite or at least 10 mM nitrate supplemented to the minimal salts growth medium. In order to obtain holocytochrome, the gene sequence encoding mature NapB was cloned in-frame with the E. coli ompA (outer membrane protein A) signal sequence. Under anaerobic conditions, NapB was secreted into the periplasmic space, with the OmpA signal peptide being correctly processed and with both haem c groups attached covalently. Unless expressed in the DegP-protease-deficient strain HM125, some of the recombinant NapB polypeptides were N-terminally truncated as a result of proteolytic activity. Under aerobic growth conditions, co-expression with the E. coli ccm (cytochrome c maturation) genes resulted in a higher yield of holocytochrome c. The pure recombinant NapB protein showed absorption maxima at 419, 522 and 550 nm in the reduced form. The midpoint reduction potentials of the two haem groups were determined to be -25 mV and -175 mV. These results support our hypothesis that the Nap system fulfils a nitrate-scavenging role in H. influenzae.

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Year:  2001        PMID: 11389694      PMCID: PMC1221913          DOI: 10.1042/0264-6021:3560851

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  40 in total

1.  Structure and characterization of Ectothiorhodospira vacuolata cytochrome b(558), a prokaryotic homologue of cytochrome b(5).

Authors:  V Kostanjevecki; D Leys; G Van Driessche; T E Meyer; M A Cusanovich; U Fischer; Y Guisez; J Van Beeumen
Journal:  J Biol Chem       Date:  1999-12-10       Impact factor: 5.157

Review 2.  Prokaryotic nitrate reduction: molecular properties and functional distinction among bacterial nitrate reductases.

Authors:  C Moreno-Vivián; P Cabello; M Martínez-Luque; R Blasco; F Castillo
Journal:  J Bacteriol       Date:  1999-11       Impact factor: 3.490

3.  Competition between Escherichia coli strains expressing either a periplasmic or a membrane-bound nitrate reductase: does Nap confer a selective advantage during nitrate-limited growth?

Authors:  L C Potter; P Millington; L Griffiths; G H Thomas; J A Cole
Journal:  Biochem J       Date:  1999-11-15       Impact factor: 3.857

4.  Different physiological roles of two independent pathways for nitrite reduction to ammonia by enteric bacteria.

Authors:  L Page; L Griffiths; J A Cole
Journal:  Arch Microbiol       Date:  1990       Impact factor: 2.552

5.  Periplasmic and membrane-bound respiratory nitrate reductases in Thiosphaera pantotropha. The periplasmic enzyme catalyzes the first step in aerobic denitrification.

Authors:  L C Bell; D J Richardson; S J Ferguson
Journal:  FEBS Lett       Date:  1990-06-04       Impact factor: 4.124

6.  The identification of cytochromes involved in the transfer of electrons to the periplasmic NO3- reductase of Rhodobacter capsulatus and resolution of a soluble NO3(-)-reductase--cytochrome-c552 redox complex.

Authors:  D J Richardson; A G McEwan; M D Page; J B Jackson; S J Ferguson
Journal:  Eur J Biochem       Date:  1990-11-26

7.  A NapC/NirT-type cytochrome c (NrfH) is the mediator between the quinone pool and the cytochrome c nitrite reductase of Wolinella succinogenes.

Authors:  J Simon; R Gross; O Einsle; P M Kroneck; A Kröger; O Klimmek
Journal:  Mol Microbiol       Date:  2000-02       Impact factor: 3.501

8.  Expression of a Desulfovibrio tetraheme cytochrome c in Escherichia coli.

Authors:  P N da Costa; C Conte; L M Saraiva
Journal:  Biochem Biophys Res Commun       Date:  2000-02-24       Impact factor: 3.575

9.  Identification of the regulatory sequence of anaerobically expressed locus aeg-46.5.

Authors:  M Choe; W S Reznikoff
Journal:  J Bacteriol       Date:  1993-02       Impact factor: 3.490

10.  Structure and function of a periplasmic nitrate reductase in Alcaligenes eutrophus H16.

Authors:  R A Siddiqui; U Warnecke-Eberz; A Hengsberger; B Schneider; S Kostka; B Friedrich
Journal:  J Bacteriol       Date:  1993-09       Impact factor: 3.490

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  6 in total

Review 1.  Structural and mechanistic insights on nitrate reductases.

Authors:  Catarina Coelho; Maria João Romão
Journal:  Protein Sci       Date:  2015-09-22       Impact factor: 6.725

2.  Regulation of nap gene expression and periplasmic nitrate reductase activity in the phototrophic bacterium Rhodobacter sphaeroides DSM158.

Authors:  Mónica Gavira; M Dolores Roldán; Francisco Castillo; Conrado Moreno-Vivián
Journal:  J Bacteriol       Date:  2002-03       Impact factor: 3.490

3.  Identification of Actinobacillus pleuropneumoniae genes important for survival during infection in its natural host.

Authors:  Brian J Sheehan; Janine T Bossé; Amanda J Beddek; Andrew N Rycroft; J Simon Kroll; Paul R Langford
Journal:  Infect Immun       Date:  2003-07       Impact factor: 3.441

Review 4.  Nitrate and periplasmic nitrate reductases.

Authors:  Courtney Sparacino-Watkins; John F Stolz; Partha Basu
Journal:  Chem Soc Rev       Date:  2014-01-21       Impact factor: 54.564

5.  NapB in excess inhibits growth of Shewanella oneidensis by dissipating electrons of the quinol pool.

Authors:  Miao Jin; Qianyun Zhang; Yijuan Sun; Haichun Gao
Journal:  Sci Rep       Date:  2016-11-18       Impact factor: 4.379

6.  NapB Restores cytochrome c biosynthesis in bacterial dsbD-deficient mutants.

Authors:  Kailun Guo; Xue Feng; Weining Sun; Sirui Han; Shihua Wu; Haichun Gao
Journal:  Commun Biol       Date:  2022-01-21
  6 in total

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