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Revision as of 20:29, 28 May 2011 editCheMoBot (talk | contribs)Bots141,565 edits Updating {{chembox}} (no changed fields - added verified revid - updated 'UNII_Ref', 'ChemSpiderID_Ref', 'StdInChI_Ref', 'StdInChIKey_Ref', 'ChEMBL_Ref', 'KEGG_Ref') per Chem/Drugbox validation (← Previous edit Revision as of 11:55, 9 July 2011 edit undoEdgar181 (talk | contribs)Extended confirmed users196,325 edits minor cleanup; SMILES added; added Category:Pyridines using HotCatNext edit →
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| CASNo = 69945-42-2 | CASNo = 69945-42-2
| PubChem =25202662 | PubChem =25202662
| SMILES = | SMILES = C1=CC(=NC(=C1)C(=O)S)C(=O)S
| PubChem = 10214455 | PubChem = 10214455
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
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}} }}
| Section2 = {{Chembox Properties | Section2 = {{Chembox Properties
| C=7|H=5|O=2|S=2
| Formula = C<sub>7</sub>H<sub>5</sub>O<sub>2</sub>S<sub>2</sub>
⚫ | Appearance =White crystalline solid
| MolarMass = 199.25 g/mol
| Density = 1.415 g/cm<sup>3</sup>
⚫ | Appearance =white crystalline
| Density = 1.415 g/cm3 | MeltingPtCL = 97
| MeltingPt = 97–99°C | MeltingPtCH = 99
| BoilingPt = 404.4°C | BoilingPtC = 404.4
| Solubility = 1000 g/L (5.02 mol/L)}} | Solubility = 1000 g/L (5.02 mol/L)}}
| Section3 = {{Chembox Hazards | Section3 = {{Chembox Hazards
| MainHazards = acidic | MainHazards = acidic
| FlashPt = 198.4◦C | FlashPt = {{convert|198.4|C|F}}
| Autoignition = }} | Autoignition = }}
}} }}
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{{reflist}} {{reflist}}


{{DEFAULTSORT:Pyridinedicarbothioic acid, 2,6-}}

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Revision as of 11:55, 9 July 2011

2,6-Pyridinedicarbothioic acid
Names
IUPAC name 2,6-pyridinedicarbothioic acid
Other names PDTC, dithiopyridinedicarbothioic acid
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
PubChem CID
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C7H5NO2S2/c9-6(11)4-2-1-3-5(8-4)7(10)12/h1-3H,(H,9,11)(H,10,12)Key: SSRIAMRLMUFTNV-UHFFFAOYSA-N
SMILES
  • O=C(S)c1nc(C(=O)S)ccc1
Properties
Chemical formula C7H5O2S2
Molar mass 185.24 g·mol
Appearance White crystalline solid
Density 1.415 g/cm
Boiling point 404.4 °C (759.9 °F; 677.5 K)
Solubility in water 1000 g/L (5.02 mol/L)
Hazards
Occupational safety and health (OHS/OSH):
Main hazards acidic
Flash point 198.4 °C (389.1 °F)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkY verify (what is  ?) Infobox references
Chemical compound

2,6-Pyridinedicarbothioic acid (PDTC) is an organosulfur compound that is produced by some bacteria. It functions as a siderophore, a small chelating agent with a high affinity for iron. Siderophores are deployed as ion scavengers for microbes. Siderophores solubilize compounds by forming strong complexes. PDTC is secreted by the soil bacteria Pseudomonas stutzeri and Pseudomonas putida.

Synthesis and biosynthesis

PDTC can be synthesized by treating the pyridine-2,6-dicarboxylic acid (or its diacid dichloride) with H2S in dry pyridine:

NC5H3(COOH)2 + 2 H2S → NC5H3(COSH)2 + 2 H2O

This produces an orange 1:1 pyridinium salt of 2,6-pyridinedicarbothioate. Treatment of this salt with acid give PDTC, which can then be extracted with dichloromethane.

The biosynthesis of PDTC remains unclear although some insights can be deduced from the genetics. It is suggested that Pseudomonas stutzeri may have acquired at least one of the genes by lateral transfer from mycobacteria. In a proposed biosynthetic sequence pyridine-2,6-dicarboxylic acid, a known bacterial metabolite, is activated as its bis-adenosine monophosphate (AMP) derivative. The sulfur donor and its activation remain uncertain.

Coordination chemistry

PDTC binds to both Fe and Fe. The ferric complex is brown, whereas the ferrous complex is blue. In the presence of air, the ferrous complex oxidizes to the ferric compound. It is iron selective as only the Fe complex is soluble in water. PDTC is produced mainly during the exponential phase of bacterial growth. The conditions at which Pseudomonas produces PDTC is 25 °C, pH=8 and sufficient aeration.

See also

References

  1. Budzikiewicz, Herbert (2010). "Microbial Siderophores". 92: 1–75. doi:10.1007/978-3-211-99661-4_1. {{cite journal}}: Cite journal requires |journal= (help)
  2. Cortese, Marc S; Caplan, Allan B; Crawford, Ronald L (2002). "Structural, functional, and evolutionary analysis of moeZ, a gene encoding an enzyme required for the synthesis of the Pseudomonas metabolite, pyridine-2,6-bis(thiocarboxylic acid)". BMC Evolutionary Biology. 2: 8. doi:10.1186/1471-2148-2-8. PMC 115864. PMID 11972321.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  3. ^ Cortese, Marc S.; Paszczynski, Andrzej; Lewis, Thomas A.; Sebat, Jonathan L.; Borek, Vladimir; Crawford, Ronald L. (2002). "Metal chelating properties of pyridine-2,6-bis(thiocarboxylic acid) produced by Pseudomonas spp. And the biological activities of the formed complexes". BioMetals. 15 (2): 103–120. doi:10.1023/A:1015241925322. PMID 12046919.
  4. ^ Budzikiewicz, H. (2003). "Heteroaromatic monothiocarboxylic acids from Pseudomonas spp". Biodegradation. 14 (2): 65–72. doi:10.1023/A:1024012015127. PMID 12877462.
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