Literature DB >> 12644498

Mutations which uncouple transport and phosphorylation in the D-mannitol phosphotransferase system of Escherichia coli K-12 and Klebsiella pneumoniae 1033-5P14.

Susanne Otte1, Annette Scholle, Sevket Turgut, Joseph W Lengeler.   

Abstract

Mutants of Escherichia coli K-12 were isolated which lack the normal phosphotransferase system-dependent catabolic pathway for D-mannitol (Mtl). In some mutants the pts genes for the general proteins enzyme I and histidine protein of the phosphoenolpyruvate-dependent carbohydrate phosphotransferase systems were deleted. Other mutants expressed truncated mannitol-specific enzymes II (II(Mtl)) which lacked the IIA(Mtl) or IIBA(Mtl) domain(s), and the mtlA genes originated either from E. coli K-12 or from Klebsiella pneumoniae 1033-5P14. The dalD gene from Klebsiella oxytoca M5a1 was cloned on single-copy plasmids and transformed into the strains described above. This gene encodes an NAD-dependent D-arabinitol dehydrogenase (DalD) which converts D-arabinitol into D-xylulose and also converts D-mannitol into D-fructose. The different strains were used to isolate mutations which allow efficient transport of mannitol through the nonphosphorylated II(Mtl) complexes by selecting for growth on this polyhydric alcohol. More than 40 different mutants were analyzed to determine their ability to grow on mannitol, as well as their ability to bind and transport free mannitol and, after restoration of the missing domain(s), their ability to phosphorylate mannitol. Four mutations were identified (E218A, E218V, H256P, and H256Y); all of these mutations are located in the highly conserved loop 5 of the IIC membrane-bound transporter, and two are located in its GIHE motif. These mutations were found to affect the various functions in different ways. Interestingly, in the presence of all II(Mtl) variants, whether they were in the truncated form or in the complete form, in the phosphorylated form or in the nonphosphorylated form, and in the wild-type form or in the mutated form, growth occurred on the low-affinity analogue D-arabinitol with good efficiency, while only the uncoupled mutated forms transported mannitol at a high rate.

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Year:  2003        PMID: 12644498      PMCID: PMC151505          DOI: 10.1128/JB.185.7.2267-2276.2003

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


  43 in total

1.  Site-directed mutagenesis of loop L3 of sucrose porin ScrY leads to changes in substrate selectivity.

Authors:  C Ulmke; J Kreth; J W Lengeler; W Welte; K Schmid
Journal:  J Bacteriol       Date:  1999-03       Impact factor: 3.490

2.  Relation between the oligomerization state and the transport and phosphorylation function of the Escherichia coli mannitol transport protein: interaction between mannitol-specific enzyme II monomers studied by complementation of inactive site-directed mutants.

Authors:  H Boer; R H ten Hoeve-Duurkens; G T Robillard
Journal:  Biochemistry       Date:  1996-10-01       Impact factor: 3.162

3.  Substrate recognition domains as revealed by active hybrids between the D-arabinitol and ribitol transporters from Klebsiella pneumoniae.

Authors:  H Heuel; S Turgut; K Schmid; J W Lengeler
Journal:  J Bacteriol       Date:  1997-10       Impact factor: 3.490

4.  The glucose transporter of the Escherichia coli phosphotransferase system. Mutant analysis of the invariant arginines, histidines, and domain linker.

Authors:  R Lanz; B Erni
Journal:  J Biol Chem       Date:  1998-05-15       Impact factor: 5.157

Review 5.  Enzymes II of the phospho enol pyruvate-dependent phosphotransferase systems: their structure and function in carbohydrate transport.

Authors:  J W Lengeler; K Jahreis; U F Wehmeier
Journal:  Biochim Biophys Acta       Date:  1994-11-01

6.  Analysis of mutations that uncouple transport from phosphorylation in enzyme IIGlc of the Escherichia coli phosphoenolpyruvate-dependent phosphotransferase system.

Authors:  G J Ruijter; G van Meurs; M A Verwey; P W Postma; K van Dam
Journal:  J Bacteriol       Date:  1992-05       Impact factor: 3.490

7.  A conserved glutamate residue, Glu-257, is important for substrate binding and transport by the Escherichia coli mannitol permease.

Authors:  C A Saraceni-Richards; G R Jacobson
Journal:  J Bacteriol       Date:  1997-02       Impact factor: 3.490

8.  Site-specific mutagenesis of residues in the Escherichia coli mannitol permease that have been suggested to be important for its phosphorylation and chemoreception functions.

Authors:  Q P Weng; J Elder; G R Jacobson
Journal:  J Biol Chem       Date:  1992-09-25       Impact factor: 5.157

9.  Molecular analysis of two fructokinases involved in sucrose metabolism of enteric bacteria.

Authors:  P Aulkemeyer; R Ebner; G Heilenmann; K Jahreis; K Schmid; S Wrieden; J W Lengeler
Journal:  Mol Microbiol       Date:  1991-12       Impact factor: 3.501

10.  Genes for D-arabinitol and ribitol catabolism from Klebsiella pneumoniae.

Authors:  H Heuel; A Shakeri-Garakani; S Turgut; J W Lengeler
Journal:  Microbiology       Date:  1998-06       Impact factor: 2.777

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  3 in total

1.  Localization of the substrate-binding site in the homodimeric mannitol transporter, EIImtl, of Escherichia coli.

Authors:  Milena Opacić; Erwin P P Vos; Ben H Hesp; Jaap Broos
Journal:  J Biol Chem       Date:  2010-06-03       Impact factor: 5.157

2.  The mannitol operon repressor MtlR belongs to a new class of transcription regulators in bacteria.

Authors:  Kemin Tan; Shonda Clancy; Maria Borovilos; Min Zhou; Stefan Hörer; Shiu Moy; Lour L Volkart; Judyth Sassoon; Ulrich Baumann; Andrzej Joachimiak
Journal:  J Biol Chem       Date:  2009-10-19       Impact factor: 5.157

Review 3.  Challenges in enzymatic route of mannitol production.

Authors:  Sheelendra Mangal Bhatt; Anand Mohan; Suresh Kumar Srivastava
Journal:  ISRN Biotechnol       Date:  2012-12-26
  3 in total

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