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Patulin

Patulin is an organic compound classified as a polyketide. It is a white powder soluble in acidic water and in organic solvents. It is a lactone that is heat-stable, so it is not destroyed by pasteurization or thermal denaturation.[2] However, stability following fermentation is lessened.[3] It is a mycotoxin produced by a variety of molds, in particular, Aspergillus and Penicillium and Byssochlamys. Most commonly found in rotting apples, the amount of patulin in apple products is generally viewed as a measure of the quality of the apples used in production. In addition, patulin has been found in other foods such as grains, fruits, and vegetables. Its presence is highly regulated.

Patulin[1]
Names
IUPAC name
4-hydroxy-4H-furo[3,2-c]pyran-2(6H)-one
Other names
2-Hydroxy-3,7-dioxabicyclo[4.3.0]nona-5,9-dien-8-one
Clairformin
Claviform
Expansine
Clavacin
Clavatin
Expansin
Gigantin
Leucopin
Patuline
Identifiers
  • 149-29-1 Y
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:74926 N
ChEMBL
  • ChEMBL294018 Y
ChemSpider
  • 4534 Y
ECHA InfoCard 100.005.215
EC Number
  • 205-735-2
KEGG
  • C16748 N
  • 4696
UNII
  • 95X2BV4W8R Y
  • DTXSID2021101
  • InChI=1S/C7H6O4/c8-6-3-4-5(11-6)1-2-10-7(4)9/h1,3,7,9H,2H2 Y
    Key: ZRWPUFFVAOMMNM-UHFFFAOYSA-N Y
  • InChI=1/C7H6O4/c8-6-3-4-5(11-6)1-2-10-7(4)9/h1,3,7,9H,2H2
    Key: ZRWPUFFVAOMMNM-UHFFFAOYAU
  • O=C\1O/C2=C/COC(O)C2=C/1
Properties
C7H6O4
Molar mass 154.12 g/mol
Appearance Compact prisms
Density 1.52 g/ml
Melting point 110 °C (230 °F; 383 K)
Soluble
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)

Biosynthesis, synthesis, and reactivity edit

Patulin is biosynthesized from 6-methylsalicylic acid via multiple chemical transformations.[4]

Isoepoxydon dehydrogenase (IDH) is an important enzyme in the multi-step biosynthesis of patulin. Its gene is present in other fungi that may potentially produce the toxin.[5] It is reactive with sulfur dioxide, so antioxidant and antimicrobial agents may be useful to destroy it.[6] Levels of nitrogen, manganese, and pH as well as abundance of necessary enzymes regulate the biosynthetic pathway of patulin.[5]

Uses edit

Patulin was originally used as an antibiotic against Gram-positive and Gram-negative bacteria, but after several toxicity reports, it is no longer used for that purpose.[7] Isolated by Nancy Atkinson in 1943, it was specifically trialed to be used against the common cold.[7] Patulin is used as a potassium-uptake inhibitor in laboratory applications.[2] Kashif Jilani and co-workers reported that patulin stimulates suicidal erythrocyte death under physiological concentrations.[8]

Sources of exposure edit

Frequently, patulin is found in apples and apple products such as juices, jams, and ciders. It has also been detected in other fruits including cherries, blueberries, plums, bananas, strawberries, and grapes.[6] Fungal growth leading to patulin production is most common on damaged fruits.[9] Patulin has also been detected in grains like barley, wheat, corn and their processed products as well as in shellfish.[6][10][full citation needed] Dietary intake of patulin from apple juice has been estimated at between 0.03 and 0.26 μg/kg bw/day in various age groups and populations.[11] Content of patulin in apple juice is estimated to be less than 10–15μg/L.[11] A number of studies have looked into comparisons of organic vs conventional harvest of apples and levels of patulin contamination.[12][13][14] For example, one study showed 0.9% of children drinking organic apple juice exceeded the tolerable daily intake (TDI) for patulin.[15][full citation needed] A recent article described detection of patulin in marine strains of Penicillium, indicating a potential risk in shellfish consumption.[10]

Toxicity edit

A subacute rodent NOAEL of 43 μg/kg body weight as well as genotoxicity studies were primarily the cause for setting limits for patulin exposure, although a range of other types of toxicity also exist.[3]

While not a particularly potent toxin, patulin is genotoxic. Some theorize that it may be a carcinogen, although animal studies have remained inconclusive.[16] Patulin has shown antimicrobial properties against some microorganisms.[1] Several countries have instituted patulin restrictions in apple products. The World Health Organization recommends a maximum concentration of 50 µg/L in apple juice.[17] In the European Union, the limit is also set at 50 micrograms per kilogram (µg/kg) in apple juice and cider, at 25 µg/kg in solid apple products, and at 10 µg/kg in products for infants and young children. These limits came into force on 1 November 2003.[18][full citation needed]

Acute edit

Patulin is toxic primarily through affinity to sulfhydryl groups (SH), which results in inhibition of enzymes. Oral LD50 in rodent models have ranged between 20 and 100 mg/kg.[3] In poultry, the oral LD50 range was reported between 50 and 170 mg/kg.[5] Other routes of exposure are more toxic, yet less likely to occur. Major acute toxicity findings include gastrointestinal problems, neurotoxicity (i.e. convulsions), pulmonary congestion, and edema.[3]

Subacute edit

Studies in rats showed decreased weight, and gastric, intestinal, and renal function changes, while repetitive doses lead to neurotoxicity. Reproductive toxicity in males was also reported.[5] A NOAEL in rodents was observed at 43μg/kg bw.[3]

Genotoxicity edit

WHO concluded that patulin is genotoxic based on variable genotoxicity data, however it is considered a group 3 carcinogen by the International Agency for Research on Cancer (IARC) since data was inconclusive.[3]

Reproduction studies edit

Patulin decreased sperm count and altered sperm morphology in the rat.[19] Also, it resulted in abortion of F1 litters in rats and mice after i.p. injection.[5] Embryotoxicity and teratogenicity were also reported in chick eggs.[5]

Immunotoxicity edit

Patulin was found to be immunotoxic in a number of animal and even human studies. Reduced cytokine secretion, oxidative burst in macrophages, increased splenic T lymphocytes, and increased neutrophil numbers are a few endpoints noticed.[5] However, dietary relevant exposure would not be likely to alter immune response.[6]

Human health edit

Although there are only very few reported cases and epidemiological data, the FDA has set an action limit of 50 ppb in cider due to its potential carcinogenicity and other reported adverse effects.[3] In humans, it was tested as an antiviral intranasally for use against the common cold with few significant adverse effects, yet also had negligible or no beneficial effect.[7]

Risk management and regulations edit

Patulin exposure can be successfully managed by following good agricultural practices such as removing mold, washing, and not using rotten or damaged apples for baking, canning, or juice production.[3][9]

US

The provisional tolerable daily intake (PTDI) for patulin was set at 0.43 µg/kg bw by the FDA[3] based on a NOAEL of 0.3 mg/kg bw per week.[3] Monte Carlo analysis was done on apple juice to compare exposure and the PTDI. Without controls or an action limit, the 90th percentile of consumers would not be above the PTDI. However, the concentration in children 1–2 years old would be three times as high as the PDTI, hence an action limit of 50 µg/kg.[3]

WHO

The World Health Organization recommends a maximum concentration of 50 µg/L in apple juice.[17]

EU

The European Union (EU) has set a maximum limit of 50μg/kg on fruit juices and drinks, while solid apple products have a limit of 25μg/kg. For certain foods intended for infants, an even lower limit of 10μg/kg is observed.

To test for patulin contamination, a variety of methods and sample preparation methods have been employed, including thin layer chromatography (TLC), gas chromatography (GC), high-performance liquid chromatography (HPLC), and capillary electrophoresis.[20]

References edit

  1. ^ a b Merck Index, 11th Edition, 7002
  2. ^ a b Patulin sigmaaldrich.com
  3. ^ a b c d e f g h i j k . www.fda.gov. Archived from the original on 2013-08-15.
  4. ^ Puel, Olivier; Galtier, Pierre; Oswald, Isabelle (2010). "Biosynthesis and Toxicological Effects of Patulin". Toxins. 2 (4): 613–631. doi:10.3390/toxins2040613. PMC 3153204. PMID 22069602.
  5. ^ a b c d e f g Puel, Olivier; Galtier, Pierre; Oswald, Isabelle P. (5 April 2010). "Biosynthesis and Toxicological Effects of Patulin". Toxins. 2 (4): 613–631. doi:10.3390/toxins2040613. PMC 3153204. PMID 22069602.
  6. ^ a b c d Llewellyn, G.C; McCay, J.A; Brown, R.D; Musgrove, D.L; Butterworth, L.F; Munson, A.E; White, K.L (1998). "Immunological evaluation of the mycotoxin patulin in female b6C3F1 mice". Food and Chemical Toxicology. 36 (12): 1107–1115. doi:10.1016/s0278-6915(98)00084-2. PMID 9862653.
  7. ^ a b c Medical Research Council. Clinical trial of patulin in the common cold. Lancet1944; ii: 373-5.
  8. ^ Lupescu, A; Jilani, K; Zbidah, M; Lang, F (2013). "Patulin-induced suicidal erythrocyte death". Cellular Physiology and Biochemistry. 32 (2): 291–9. doi:10.1159/000354437. PMID 23942252.
  9. ^ a b . Archived from the original on 2013-10-18. Retrieved 2013-11-25.
  10. ^ a b Pouchous et al. Shellfish
  11. ^ a b Wouters, FA, and Speijers, GJA. JECFA Monograph on Patulin. World Health Organization Food Additives Series 35 (http://www.inchem.org/documents/jecfa/jecmono/v26je10.htm)
  12. ^ Pique, E., et al. Occurrence of patulin in organic and conventional apple juice. Risk Assessment. Recent Advances in Pharmaceutical Sciences, III, 2013: 131–144.
  13. ^ Piemontese, L.; Solfrizzo, M.; Visconti, A. (2005-05-01). "Occurrence of patulin in conventional and organic fruit products in Italy and subsequent exposure assessment". Food Additives and Contaminants. 22 (5): 437–442. doi:10.1080/02652030500073550. ISSN 0265-203X. PMID 16019815. S2CID 31155096.
  14. ^ Piqué, E; Vargas-Murga, L; Gómez-Catalán, J; Lapuente, Jd; Llobet, JM (October 2013). "Occurrence of patulin in organic and conventional apple-based food marketed in Catalonia and exposure assessment". Food and Chemical Toxicology. 60: 199–204. doi:10.1016/j.fct.2013.07.052. PMID 23900007.
  15. ^ Beark et al 2007
  16. ^ "Patulin: a Mycotoxin in Apples". Perishables Handling Quarterly (91): 5. August 1997
  17. ^ a b "Foodborne hazards (World Health Organization". Retrieved 2007-01-22.
  18. ^ Patulin information leaf from Fermentek
  19. ^ Selmanoglu, G (2006). "Evaluation of the reproductive toxicity of patulin in growing male rats". Food Chem. Toxicol. 44 (12): 2019–2024. doi:10.1016/j.fct.2006.06.022. PMID 16905234.
  20. ^ Baert, Katleen; De Meulenaer, Bruno; Verdonck, Frederik; Huybrechts, Inge; De Henauw, Stefaan; Vanrolleghem, Peter A.; Debevere, Johan; Devlieghere, Frank (2007). "Variability and uncertainty assessment of patulin exposure for preschool children in Flanders". Food and Chemical Toxicology. 45 (9): 1745–1751. doi:10.1016/j.fct.2007.03.008. PMID 17459555.

External links edit

patulin, claviform, redirects, here, botany, zoology, term, glossary, entomology, terms, clavate, organic, compound, classified, polyketide, white, powder, soluble, acidic, water, organic, solvents, lactone, that, heat, stable, destroyed, pasteurization, therm. Claviform redirects here For the botany and zoology term see Glossary of entomology terms clavate Patulin is an organic compound classified as a polyketide It is a white powder soluble in acidic water and in organic solvents It is a lactone that is heat stable so it is not destroyed by pasteurization or thermal denaturation 2 However stability following fermentation is lessened 3 It is a mycotoxin produced by a variety of molds in particular Aspergillus and Penicillium and Byssochlamys Most commonly found in rotting apples the amount of patulin in apple products is generally viewed as a measure of the quality of the apples used in production In addition patulin has been found in other foods such as grains fruits and vegetables Its presence is highly regulated Patulin 1 NamesIUPAC name 4 hydroxy 4H furo 3 2 c pyran 2 6H oneOther names 2 Hydroxy 3 7 dioxabicyclo 4 3 0 nona 5 9 dien 8 one ClairforminClaviformExpansineClavacinClavatinExpansinGigantinLeucopinPatulineIdentifiersCAS Number 149 29 1 Y3D model JSmol Interactive imageChEBI CHEBI 74926 NChEMBL ChEMBL294018 YChemSpider 4534 YECHA InfoCard 100 005 215EC Number 205 735 2KEGG C16748 NPubChem CID 4696UNII 95X2BV4W8R YCompTox Dashboard EPA DTXSID2021101InChI InChI 1S C7H6O4 c8 6 3 4 5 11 6 1 2 10 7 4 9 h1 3 7 9H 2H2 YKey ZRWPUFFVAOMMNM UHFFFAOYSA N YInChI 1 C7H6O4 c8 6 3 4 5 11 6 1 2 10 7 4 9 h1 3 7 9H 2H2Key ZRWPUFFVAOMMNM UHFFFAOYAUSMILES O C 1O C2 C COC O C2 C 1PropertiesChemical formula C 7H 6O 4Molar mass 154 12 g molAppearance Compact prismsDensity 1 52 g mlMelting point 110 C 230 F 383 K Solubility in water SolubleExcept where otherwise noted data are given for materials in their standard state at 25 C 77 F 100 kPa N verify what is Y N Infobox references Contents 1 Biosynthesis synthesis and reactivity 2 Uses 3 Sources of exposure 4 Toxicity 4 1 Acute 4 2 Subacute 4 3 Genotoxicity 4 4 Reproduction studies 4 5 Immunotoxicity 4 6 Human health 5 Risk management and regulations 6 References 7 External linksBiosynthesis synthesis and reactivity editPatulin is biosynthesized from 6 methylsalicylic acid via multiple chemical transformations 4 Isoepoxydon dehydrogenase IDH is an important enzyme in the multi step biosynthesis of patulin Its gene is present in other fungi that may potentially produce the toxin 5 It is reactive with sulfur dioxide so antioxidant and antimicrobial agents may be useful to destroy it 6 Levels of nitrogen manganese and pH as well as abundance of necessary enzymes regulate the biosynthetic pathway of patulin 5 Uses editPatulin was originally used as an antibiotic against Gram positive and Gram negative bacteria but after several toxicity reports it is no longer used for that purpose 7 Isolated by Nancy Atkinson in 1943 it was specifically trialed to be used against the common cold 7 Patulin is used as a potassium uptake inhibitor in laboratory applications 2 Kashif Jilani and co workers reported that patulin stimulates suicidal erythrocyte death under physiological concentrations 8 Sources of exposure editFrequently patulin is found in apples and apple products such as juices jams and ciders It has also been detected in other fruits including cherries blueberries plums bananas strawberries and grapes 6 Fungal growth leading to patulin production is most common on damaged fruits 9 Patulin has also been detected in grains like barley wheat corn and their processed products as well as in shellfish 6 10 full citation needed Dietary intake of patulin from apple juice has been estimated at between 0 03 and 0 26 mg kg bw day in various age groups and populations 11 Content of patulin in apple juice is estimated to be less than 10 15mg L 11 A number of studies have looked into comparisons of organic vs conventional harvest of apples and levels of patulin contamination 12 13 14 For example one study showed 0 9 of children drinking organic apple juice exceeded the tolerable daily intake TDI for patulin 15 full citation needed A recent article described detection of patulin in marine strains of Penicillium indicating a potential risk in shellfish consumption 10 Toxicity editA subacute rodent NOAEL of 43 mg kg body weight as well as genotoxicity studies were primarily the cause for setting limits for patulin exposure although a range of other types of toxicity also exist 3 While not a particularly potent toxin patulin is genotoxic Some theorize that it may be a carcinogen although animal studies have remained inconclusive 16 Patulin has shown antimicrobial properties against some microorganisms 1 Several countries have instituted patulin restrictions in apple products The World Health Organization recommends a maximum concentration of 50 µg L in apple juice 17 In the European Union the limit is also set at 50 micrograms per kilogram µg kg in apple juice and cider at 25 µg kg in solid apple products and at 10 µg kg in products for infants and young children These limits came into force on 1 November 2003 18 full citation needed Acute edit Patulin is toxic primarily through affinity to sulfhydryl groups SH which results in inhibition of enzymes Oral LD50 in rodent models have ranged between 20 and 100 mg kg 3 In poultry the oral LD50 range was reported between 50 and 170 mg kg 5 Other routes of exposure are more toxic yet less likely to occur Major acute toxicity findings include gastrointestinal problems neurotoxicity i e convulsions pulmonary congestion and edema 3 Subacute edit Studies in rats showed decreased weight and gastric intestinal and renal function changes while repetitive doses lead to neurotoxicity Reproductive toxicity in males was also reported 5 A NOAEL in rodents was observed at 43mg kg bw 3 Genotoxicity edit WHO concluded that patulin is genotoxic based on variable genotoxicity data however it is considered a group 3 carcinogen by the International Agency for Research on Cancer IARC since data was inconclusive 3 Reproduction studies edit Patulin decreased sperm count and altered sperm morphology in the rat 19 Also it resulted in abortion of F1 litters in rats and mice after i p injection 5 Embryotoxicity and teratogenicity were also reported in chick eggs 5 Immunotoxicity edit Patulin was found to be immunotoxic in a number of animal and even human studies Reduced cytokine secretion oxidative burst in macrophages increased splenic T lymphocytes and increased neutrophil numbers are a few endpoints noticed 5 However dietary relevant exposure would not be likely to alter immune response 6 Human health edit Although there are only very few reported cases and epidemiological data the FDA has set an action limit of 50 ppb in cider due to its potential carcinogenicity and other reported adverse effects 3 In humans it was tested as an antiviral intranasally for use against the common cold with few significant adverse effects yet also had negligible or no beneficial effect 7 Risk management and regulations editPatulin exposure can be successfully managed by following good agricultural practices such as removing mold washing and not using rotten or damaged apples for baking canning or juice production 3 9 USThe provisional tolerable daily intake PTDI for patulin was set at 0 43 µg kg bw by the FDA 3 based on a NOAEL of 0 3 mg kg bw per week 3 Monte Carlo analysis was done on apple juice to compare exposure and the PTDI Without controls or an action limit the 90th percentile of consumers would not be above the PTDI However the concentration in children 1 2 years old would be three times as high as the PDTI hence an action limit of 50 µg kg 3 WHOThe World Health Organization recommends a maximum concentration of 50 µg L in apple juice 17 EUThe European Union EU has set a maximum limit of 50mg kg on fruit juices and drinks while solid apple products have a limit of 25mg kg For certain foods intended for infants an even lower limit of 10mg kg is observed To test for patulin contamination a variety of methods and sample preparation methods have been employed including thin layer chromatography TLC gas chromatography GC high performance liquid chromatography HPLC and capillary electrophoresis 20 References edit a b Merck Index 11th Edition 7002 a b Patulin sigmaaldrich com a b c d e f g h i j k Patulin in Apple Juice Apple Juice Concentrates and Apple Juice Products www fda gov Archived from the original on 2013 08 15 Puel Olivier Galtier Pierre Oswald Isabelle 2010 Biosynthesis and Toxicological Effects of Patulin Toxins 2 4 613 631 doi 10 3390 toxins2040613 PMC 3153204 PMID 22069602 a b c d e f g Puel Olivier Galtier Pierre Oswald Isabelle P 5 April 2010 Biosynthesis and Toxicological Effects of Patulin Toxins 2 4 613 631 doi 10 3390 toxins2040613 PMC 3153204 PMID 22069602 a b c d Llewellyn G C McCay J A Brown R D Musgrove D L Butterworth L F Munson A E White K L 1998 Immunological evaluation of the mycotoxin patulin in female b6C3F1 mice Food and Chemical Toxicology 36 12 1107 1115 doi 10 1016 s0278 6915 98 00084 2 PMID 9862653 a b c Medical Research Council Clinical trial of patulin in the common cold Lancet1944 ii 373 5 Lupescu A Jilani K Zbidah M Lang F 2013 Patulin induced suicidal erythrocyte death Cellular Physiology and Biochemistry 32 2 291 9 doi 10 1159 000354437 PMID 23942252 a b Patulin Archived from the original on 2013 10 18 Retrieved 2013 11 25 a b Pouchous et al Shellfish a b Wouters FA and Speijers GJA JECFA Monograph on Patulin World Health Organization Food Additives Series 35 http www inchem org documents jecfa jecmono v26je10 htm Pique E et al Occurrence of patulin in organic and conventional apple juice Risk Assessment Recent Advances in Pharmaceutical Sciences III 2013 131 144 Piemontese L Solfrizzo M Visconti A 2005 05 01 Occurrence of patulin in conventional and organic fruit products in Italy and subsequent exposure assessment Food Additives and Contaminants 22 5 437 442 doi 10 1080 02652030500073550 ISSN 0265 203X PMID 16019815 S2CID 31155096 Pique E Vargas Murga L Gomez Catalan J Lapuente Jd Llobet JM October 2013 Occurrence of patulin in organic and conventional apple based food marketed in Catalonia and exposure assessment Food and Chemical Toxicology 60 199 204 doi 10 1016 j fct 2013 07 052 PMID 23900007 Beark et al 2007 Patulin a Mycotoxin in Apples Perishables Handling Quarterly 91 5 August 1997 a b Foodborne hazards World Health Organization Retrieved 2007 01 22 Patulin information leaf from Fermentek Selmanoglu G 2006 Evaluation of the reproductive toxicity of patulin in growing male rats Food Chem Toxicol 44 12 2019 2024 doi 10 1016 j fct 2006 06 022 PMID 16905234 Baert Katleen De Meulenaer Bruno Verdonck Frederik Huybrechts Inge De Henauw Stefaan Vanrolleghem Peter A Debevere Johan Devlieghere Frank 2007 Variability and uncertainty assessment of patulin exposure for preschool children in Flanders Food and Chemical Toxicology 45 9 1745 1751 doi 10 1016 j fct 2007 03 008 PMID 17459555 External links editPatulin Archived 2017 12 19 at the Wayback Machine Food Safety Watch Retrieved from https en wikipedia org w index php title Patulin amp oldid 1195935216, wikipedia, wiki, book, books, library,

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