Difference between revisions of "Mdh"
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** pGP1123 (N-terminal Strep-tag, for [[SPINE]], purification from ''B. subtilis'', in [[pGP380]]) (available in [[Stülke]] lab)  | ** pGP1123 (N-terminal Strep-tag, for [[SPINE]], purification from ''B. subtilis'', in [[pGP380]]) (available in [[Stülke]] lab)  | ||
** for expression, purification in ''E. coli'' with N-terminal His-tag, in [[pWH844]]: pGP385, available in [[Stülke]] lab  | ** for expression, purification in ''E. coli'' with N-terminal His-tag, in [[pWH844]]: pGP385, available in [[Stülke]] lab  | ||
| − | |||
** pGP1755 (expression / purification of Mdh-S149A, with N-terminal His-tag from ''E. coli'', in [[pWH844]]), available in [[Stülke]] lab  | ** pGP1755 (expression / purification of Mdh-S149A, with N-terminal His-tag from ''E. coli'', in [[pWH844]]), available in [[Stülke]] lab  | ||
| − | + | ** pGP1764 (for expression, purification in ''E. coli'' with N-terminal Strep-tag, in [[pGP172]], available in [[Stülke]] lab)   | |
| + | |||
* '''lacZ fusion:'''  | * '''lacZ fusion:'''  | ||
Revision as of 14:12, 4 November 2010
-  Description: malate dehydrogenase 
 
| Gene name | mdh | 
| Synonyms | citH | 
| Essential | no | 
| Product | malate dehydrogenase | 
| Function | TCA cycle | 
|  Metabolic function and regulation of this protein in SubtiPathways:  Central C-metabolism  | |
| MW, pI | 33 kDa, 4.727 | 
| Gene length, protein length | 936 bp, 312 aa | 
| Immediate neighbours | phoP, icd | 
| Get the DNA and protein sequences  (Barbe et al., 2009)  | |
 Genetic context  
  This image was kindly provided by SubtiList 
 | |
Contents
The gene
Basic information
- Locus tag: BSU29120
 
Phenotypes of a mutant
Database entries
- DBTBS entry: [1]
 
- SubtiList entry: [2]
 
Additional information
The protein
Basic information/ Evolution
- Catalyzed reaction/ biological activity: (S)-malate + NAD+ = oxaloacetate + NADH (according to Swiss-Prot)
 
- Protein family: MDH type 3 family (according to Swiss-Prot)
 
- Paralogous protein(s):
 
Extended information on the protein
- Kinetic information: Reversible Michaelis-Menten PubMed
 
- Domains:
 
- Modification: phosphorylation on Ser-149 PubMed
 
- Cofactor(s):
 
- Effectors of protein activity:
 
- Interactions:
 
- Localization: cytoplasm (according to Swiss-Prot), membrane associated PubMed
 
Database entries
- Structure: 1EMD (E.coli)
 
- UniProt: P49814
 
- KEGG entry: [3]
 
- E.C. number: 1.1.1.37
 
Additional information
The enzyme is a tetramer PubMed
Expression and regulation
- Regulation:
 
- Regulatory mechanism:
 
- Additional information:
 
Biological materials
- Mutant: GP719 (spc), available in Stülke lab
 
-  Expression vector:
- pGP1123 (N-terminal Strep-tag, for SPINE, purification from B. subtilis, in pGP380) (available in Stülke lab)
 - for expression, purification in E. coli with N-terminal His-tag, in pWH844: pGP385, available in Stülke lab
 - pGP1755 (expression / purification of Mdh-S149A, with N-terminal His-tag from E. coli, in pWH844), available in Stülke lab
 - pGP1764 (for expression, purification in E. coli with N-terminal Strep-tag, in pGP172, available in Stülke lab)
 
 
- lacZ fusion:
 
- GFP fusion:
 
- two-hybrid system: B. pertussis adenylate cyclase-based bacterial two hybrid system (BACTH), available in Stülke lab
 
- Antibody:
 
Labs working on this gene/protein
Your additional remarks
References
Frederik M Meyer, Jan Gerwig, Elke Hammer, Christina Herzberg, Fabian M Commichau, Uwe Völker, Jörg Stülke  
Physical interactions between tricarboxylic acid cycle enzymes in Bacillus subtilis: evidence for a metabolon. 
Metab Eng: 2011, 13(1);18-27 
[PubMed:20933603]
  [WorldCat.org]
 [DOI]
 (I p)
Hannes Hahne, Susanne Wolff, Michael Hecker, Dörte Becher  
From complementarity to comprehensiveness--targeting the membrane proteome of growing Bacillus subtilis by divergent approaches. 
Proteomics: 2008, 8(19);4123-36 
[PubMed:18763711]
  [WorldCat.org]
 [DOI]
 (I p)
Boris Macek, Ivan Mijakovic, Jesper V Olsen, Florian Gnad, Chanchal Kumar, Peter R Jensen, Matthias Mann  
The serine/threonine/tyrosine phosphoproteome of the model bacterium Bacillus subtilis. 
Mol Cell Proteomics: 2007, 6(4);697-707 
[PubMed:17218307]
  [WorldCat.org]
 [DOI]
 (P p)
Hyun-Jin Kim, Agnes Roux, Abraham L Sonenshein  
Direct and indirect roles of CcpA in regulation of Bacillus subtilis Krebs cycle genes. 
Mol Microbiol: 2002, 45(1);179-90 
[PubMed:12100558]
  [WorldCat.org]
 [DOI]
 (P p)
C Jourlin-Castelli, N Mani, M M Nakano, A L Sonenshein  
CcpC, a novel regulator of the LysR family required for glucose repression of the citB gene in Bacillus subtilis. 
J Mol Biol: 2000, 295(4);865-78 
[PubMed:10656796]
  [WorldCat.org]
 [DOI]
 (P p)
S Jin, M De Jesús-Berríos, A L Sonenshein  
A Bacillus subtilis malate dehydrogenase gene. 
J Bacteriol: 1996, 178(2);560-3 
[PubMed:8550482]
  [WorldCat.org]
 [DOI]
 (P p)
S Jin, A L Sonenshein  
Transcriptional regulation of Bacillus subtilis citrate synthase genes. 
J Bacteriol: 1994, 176(15);4680-90 
[PubMed:8045899]
  [WorldCat.org]
 [DOI]
 (P p)
A K Tyagi, F A Siddiqui, T A Venkitasubramanian  
Studies on the purification and characterization of malate dehydrogenase from Mycobacterium phlei. 
Biochim Biophys Acta: 1977, 485(2);255-67 
[PubMed:922015]
  [WorldCat.org]
 [DOI]
 (P p)
A YOSHIDA  
ENZYMIC PROPERTIES OF MALATE DEHYDROGENASE OF BACILLUS SUBTILIS. 
J Biol Chem: 1965, 240;1118-24 
[PubMed:14284712]
  [WorldCat.org]
   (P p)
