Chitin%20is%20a%20polysaccharide;%20it%20is%20synthesized%20from%20units%20of%20N-acetylglucosamine%20(more%20completely,%20N-acetyl-D-glucos-2-amine).%20These%20units%20form%20covalent%20 - PowerPoint PPT Presentation

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Chitin%20is%20a%20polysaccharide;%20it%20is%20synthesized%20from%20units%20of%20N-acetylglucosamine%20(more%20completely,%20N-acetyl-D-glucos-2-amine).%20These%20units%20form%20covalent%20

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Title: Chitin%20is%20a%20polysaccharide;%20it%20is%20synthesized%20from%20units%20of%20N-acetylglucosamine%20(more%20completely,%20N-acetyl-D-glucos-2-amine).%20These%20units%20form%20covalent%20


1
???????????????????????
2
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  • Chitin is a polysaccharide it is synthesized
    from units of N-acetylglucosamine (more
    completely, N-acetyl-D-glucos-2-amine). These
    units form covalent ß-1,4 linkages (similar to
    the linkages between glucose units forming
    cellulose).
  • ??????????(???chitin ?natural chitosan and
    modified chitosan?glucosamine?N-acetyl
    glucosamine)????????????????????????????
  • A type of polysaccharide (sugar molecule) that is
    made by some plants and animals. The hard outer
    shell of shrimp, lobsters, and many insects is
    made of chitin.

3
???
  • ???(C8H13O5)n ,?????????,????,???8000?ß??????????,
    ?????????????????
  • ???????????????????????????????????????????????

4
(No Transcript)
5
???(chitin)
  • ???(chitin)?????????,?N-??????(N-acetyl
    glucosamine)?????, ??ß1-4??????????,??????????????
    ?????????
  • ???????????,??????????????????????????????????,???
    ?(?????,????,chitosan),????(polymers)???(oligomers
    )???(monomers),?????????????????????,?????????????
    ??????40??,??????40???????????

6
?????????
  • ????????????????,?????????????
  • N-??-D-????????,???ß-1,4??(?????????????????),????
    ??????????????????????????????
  • ?????????????????,??????????

7
?????????
  • ????????,???????,??????,???????
  • ??????????????,?????????????,?????????????????????
    ?,???????????,???????????????

8
?????????
  • ?????????????????????????????????????
  • ???????????????????
  • ????????,??????????????????????

9
????--??
  • ???????(?????????????????,?????)?????
  • ?????????????????????????????????
  • ???????????????Chitin????????chitine?
  • ?????1836?????????chiton?,??????,???????khiton,???
    ??????????

10
???????
  • ??????????
  • ????????????
  • ???????????????
  • ????????????
  • ??????????????????
  • ????????????????

11
??????
  • ??????????????????????
  • ?????????,???????????,??????????????????

12
?????????
  • ????????????????(exoskeloton),???,?????????????,??
    ????????Chitin?????Chiosan?
  • ????????????,??????????????????????,????????????
  • ?????????????????????micelle(??? )
  • ???????????????,???????????????????

13
???????
  • ??????????????4751,?????????3241???
  • ?????????,???1g?????????12g??????
  • ????????????,?????????,????????????????

14
Chitin was first investigated in 1811
  • Chitin was first investigated in 1811 by
    Professor Henri Braconnott, who discovered it in
    the cell walls of mushrooms.
  • In the 1830s, it was isolated in insects and
    named chitin. Chitosan, a derivative of chitin,
    was produced in 1859, and since then, research
    has been conducted to learn about the properties
    of chitin and chitosan and develop commercial
    applications for their use.

15
arthropods
  • Like all arthropods (the large group which
    includes insects, scorpions, shrimp, and
    lobsters), horseshoe crabs have a hard outer
    shell, or exoskeleton, that provides protection
    from predators.
  • Millions of tightly interwoven strands of a
    cellulose-like material called chitin serve as a
    tough and flexible glue that holds together the
    shell.
  • The chitin in horseshoe crabs is favored for
    research over that found in other arthropods
    because it is very pure.

16
Chitin is natural, non-toxic
  • The combination of chitin's remarkable properties
    makes it extremely versatile.
  • Chitin is natural, non-toxic, non-allergenic,
    anti-microbial, and biodegradable.
  • It has a strong positive charge, which allows it
    to bind with negatively charged surfaces or
    materials, including metals, skin, and
    macromolecules such as proteins.

17
Cellulose, chitin, and starch
  • Cellulose, chitin, and starch are the three most
    abundant organic compounds in nature. Cellulose
    and starch are key carbohydrates that plants use
    as a food source and to build cell walls.
  • Chemically, chitin is a polysaccharide. A
    polysaccharide is a polymer a large molecule
    consisting of smaller (and in this case, sugar)
    molecules strung together.

18
chitosan
  • Chitin can be processed into many derivatives,
    the most readily available being chitosan, which
    is formed when chitin is heated with a chemical
    solution.
  • Chitosan has some advantages over chitin because
    it is more water-soluble.

19
chitin-related products
  • By the 1940s, almost 50 patents had been filed
    for chitin-related products.
  • But commercial development of chitin proceeded
    slowly, partly because synthetic products were
    already in use in some applications, and there
    was a lack of strong federal support for chitin
    research and the development of chitin products.

20
the thousands of tons of shellfish waste produced
annually
  • In the mid-1970s, however, environmental
    regulations were passed to limit the dumping of
    untreated shellfish wastes in coastal waters,
    thus making the processing of chitin from
    shellfish waste an economical way to comply with
    the regulations and dispose of the thousands of
    tons of shellfish waste produced annually.

21
15 major processors
  • Today, nearly 200 patents have been issued in the
    United States, in addition to those issued in
    several other countries worldwide, and there are
    nearly 15 major processors of chitin and chitosan
    around the world.

22
wound-healing properties
  • Early on it was found that chitin had
    wound-healing properties.
  • By the mid-1950s, chitin-coated sutures were
    being used, which enhanced healing time by 35 to
    50.
  • In the 1970s, researchers with the University of
    Delaware Sea Grant College Program developed a
    method to spin pure chitin filaments.

23
new chitin sutures
  • These new chitin sutures could be absorbed by the
    body, eliminating the need for surgical removal.
  • A Japanese firm bought the patent rights, and
    suture materials are now manufactured in Japan.

24
accelerate healing and reduce pain
  • In addition, this firm uses chitin to make
    dressings for burns, surface wounds, and
    skin-graft donor sites, which dramatically
    accelerate healing and reduce pain compared to
    standard treatments where the dressings must be
    removed.

25
artificial blood vessels
  • Other medical uses for chitin include
    anti-bacterial sponges and hospital dressings,
    artificial blood vessels, contact lenses, tumor
    inhibition, dental plaque inhibition, and blood
    cholesterol control.
  • Household products include sponges, diapers,
    feminine napkins, and tampons.

26
Water Treatment
  • Water Purification As a polymer, chitosan's
    natural tendency is to form long chains of
    molecules with positive charges, which act like
    hooks.
  • These natural hooks catch organic materials, such
    as oils, detergents, and other contaminants
    suspended in water.
  • The material then coagulates to form flakes that
    are easily filtered out. Filtration companies are
    using chitin in clarifiers to help filter
    particulates and chemicals from water.

27
Wastewater Treatment In Japan
  • chitosan was first used for wastewater treatment
    because of its metal-binding properties.
  • It is also good for cleaning up toxic organic
    compounds, such as PCBs.

28
Dietary Supplements
  • Chitosan has properties similar to plant fiber
    and can significantly bind fat, acting like a
    sponge in the digestive tract.
  • It is not digestible itself and the bound fat
    leaves via the body without ever entering the
    bloodstream.

29
Cosmetics
  • Make-up powder nail polish moisturizers face,
    hand, and body creams and toothpaste are just a
    few consumer products that might contain chitin.

30
Agriculture
  • Seeds treated with chitosan are larger and
    stronger and more resistant to fungal diseases.
  • Treating seeds with chitin can increase crop
    yields by up to 50.

31
feed mixtures
  • Chitin is added to commercial feed mixtures
    containing whey, a by-product of the cheese
    industry.
  • Many animals find it hard to digest the
    high-lactose whey.
  • But chitin supports the growth of beneficial
    microorganisms in the animals' digestive tract
    these bacteria produce enzymes that help the
    animals digest whey.

32
?????
  • ??????????????,?????(????????????)???????????,????
    ???????????????,
  • ???????????????????????????,??????????????????????
    ??????????
  • ????????????????????????????????????????????????,?
    ??????????

33
???????????
  • ????
  • Mitchell ??1959????????(chitin)????(chitosan)??
    ?????Fusarium spp., ?Allan ?Hadwiger
    ??????????????????????????????????????????????????
    S. aureus? Bacillus cereus? Escherichia
    coli?Vibro cholerae?Listeria monoctogenes ? ?

34
???????
  • ?????????????????????(-NH3)????????????????????
  • ????????????,????????,?????????????????

35
???????
  • ??????????????????????pH????????,???,????????????
    ???????,????????????????,??????????????????????

36
???????
  • ??????????????????????????????
  • ????????????????????????,????????????????????
  • ???????????????????,??80?60?????????Pseudomonas
    fluorescens ? Shigella sonnei ????,
    80???????????????????60 ???????????

37
?????
  • Kender ?Hadwiger ??????????????????????(degree
    of polymerization DP)????6???????????????????????
    ??
  • ????(M.W. 685kDa, DDA 89 ))??????????????????????
    ??,???????????,???????????10 kDa????????
  • ?????????????????????????????????????????????

38
?????????
  • ???????????,?????????????????????????????????,????
    ???????????????,??????????????????

39
?????
  • ??????????????????,?????????,???????????
  • ??????????,?????????????????????????????,Kanauchi?
    ????? ?????????????????????(micelle),????????????
    ????,?pH????????????????(gel)??,????????????,????(
    gel)?????????????????????
  • ???????C???,?????????????,??????,???????

40
???????
  • ???????????????,??????????(??),
    ??????????C?????????????
  • ??????????????????????,??????????????????,?????,??
    ??????????

41
???.??????
  • ?????????????,?????????????,??300 kDa? 20 kDa? 8
    kDa?600 Da???????????????????8 kDa??????????????,6
    00 Da?????
  • ???20 kDa ??????????????Ikeda???2-50
    kDa??????????????????,??????????2 kDa????????
  • ????8 kDa??????????????220 kDa???
  • ?Lehoux ? Grondin ????????750 kDa?????????????????
    ?????,????2000 kDa??????

42
???????????
  • ????????,????????????????????????????????????????
    ????,??????T?????????????
  • ?Mori????????????????????????????-8
    (Interleukin-8),???N-????????????????
  • ????N-?????????????????????(NO)????????????
  • ?????????????T????????????????

43
?????
  • ???????????????????,?????????????????,????????????
    ?????????????????????????
  • ???????????????,??????????????,???????????????,??c
    hitinase ?pisatin? phytoalexin polyphenolic,ß-gluc
    anase ???????????????

44
?????????
  • Ghaouth??? ???????????????????chitinase?
    chitosanase ?ß-1,3 glucanase ????,????Pythiun
    aphanidermatum ??????????
  • ???????????pisatin ?????Fusarium solani ??
  • ?????????phytoalexin?????????????????,?phytoalexin
    ??????????????????????????????,
  • ???????????????????????????????
  • ???????????????????????????????????????

45
????
  • ????????????????????
  • ???????? ?????(Colloid titration)??????(Direct
    titration)???????(UV spectrophoto- metric
    method)??
  • ?????????????????????????(infrared
    spectroscopy)????????(NMR spectroscopy)????????(HP
    LC) ??

46
???????????
  • ???????????????????????????????????????,??E.coli
    ???????
  • 2???,????E.coli??????(??????????0.002
    ),?????30???????,???NB????37???24??,???????????

47
????58.4 kDa??????
  • ??????? E. coli ????????????,??????????????????58.
    4 kDa?????????????????
  • ???????????S. aureus ??????????????

48
????
  • ?0.05g (150-400 mesh) ??????????2.5ml 0.1N
    HC???????20g??,?????????pH2
  • ???????37??????2??,???16 ml 10mM PBS ????
  • ??pH?7.00.2,??????37 oC????30??
  • ?2500rpm??30???, ????????oil/gel(oilchitosan)/wa
    ter??,?????????????
  • ?? Binding Index oil bound (g) / chitosan (g)
    oil bound????(20g)-????????????

49
?????????
  • ??????,?????????,??????????????????,??????????????
    ????????????????

50
2????????
  • ???????2??????????????????????????,?????20???????
    ???,????????(Fusarium oxysporum)????????????
  • ???????????????????????
  • ????????????????????????(?????????)
    ???????????????????200?????????1800???????????????

51
???????????
  • ??????????????????????
  • ????????????????????,??????????,??????????????????
    ???????????????,?????????????

52
???
  • ?????????????????????????????????????????????,????
    ??????????????????,???????????????????
  • ???????????????????????????????????????????????
  • ?????????????????????????????????????????????????
    ???????,?????????
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