X-Gluc

X-Gluc

Names
IUPAC name 5-Bromo-4-chloro-1H-indol-3-yl β-D-glucopyranosiduronic acid
Other names 5-Bromo-4-chloro-3-indolyl-β-D-glucuronide
Identifiers
CAS Registry Number	18656-89-8 Y 114162-64-0 (cyclohexylammonium salt) Y
ChemSpider	2015360
InChI InChI=1S/C14H13BrClNO7/c15-4-1-2-5-7(8(4)16)6(3-17-5)23-14-11(20)9(18)10(19)12(24-14)13(21)22/h1-3,9-12,14,17-20H,(H,21,22)/t9-,10-,11+,12-,14+/m0/s1 Key: DHJFFLKPAYHPHU-BYNIDDHOSA-N InChI=1/C14H13BrClNO7/c15-4-1-2-5-7(8(4)16)6(3-17-5)23-14-11(20)9(18)10(19)12(24-14)13(21)22/h1-3,9-12,14,17-20H,(H,21,22)/t9-,10-,11+,12-,14+/m0/s1 Key: DHJFFLKPAYHPHU-BYNIDDHOBP
Jmol-3D images	Image
PubChem	2733579
SMILES Brc3ccc2c(c(O[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]1O)cn2)c3Cl
Properties
Molecular formula	C14H13BrClNO7
Molar mass	422.61 g·mol−1
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Infobox references

X-Gluc is a chemical compound with the molecular formula C₁₄H₁₃BrClNO₇. It is used as a reagent to detect β-glucuronidase, an enzyme produced by the E. coli bacterium. It is used to detect E. coli contamination in food, water and the urinary tract. In addition, it is widely used in molecular biology experiments to mark and select the expression of target genes (GUS reporter system).^[1]

It is often preferred to other detection methods because it is fast (24 hour testing), relatively accurate ( <1% false negatives and <5% false positives ) and the result is easy to observe and interpret. The reagent is safe to transport and easy to store.

See also

• Bacteriological water analysis
• X-gal

References

External links

• X-Gluc lab exercise, Susan J Karcher, Purdue University
• Histochemical localization of GUS reporter activity in plant tissues, Stanislav Vitha, Texas A&M University
• X-Gluc characteristics and applications