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Bacterial Morphology and Structure

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    Bacterial Morphology and StructureBacterial Morphology and Structure

    Xiao-Kui Guo PhD

    http://basic.shsmu.edu.cn/passw/micro2/index.asp 

    http://basic.shsmu.edu.cn/passw/micro2/index.asphttp://basic.shsmu.edu.cn/passw/micro2/index.asphttp://basic.shsmu.edu.cn/passw/micro2/index.asphttp://basic.shsmu.edu.cn/passw/micro2/index.asphttp://basic.shsmu.edu.cn/passw/micro2/index.asphttp://basic.shsmu.edu.cn/passw/micro2/index.asphttp://basic.shsmu.edu.cn/passw/micro2/index.asphttp://basic.shsmu.edu.cn/passw/micro2/index.asphttp://basic.shsmu.edu.cn/passw/micro2/index.asphttp://basic.shsmu.edu.cn/passw/micro2/index.asp

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    SIZE OF BACTERIASIZE OF BACTERIA

    Unit for measurement :

    Micron or micrometer!m:"!m#"$-%mm 

    &i'e:

    (aries with )inds of bacteria and

    a*so re*ated to their a+e and externa*en,ironment.

    occi: sphere "!m

    aci**i: rods $.-" !m in width -% !m in *en+th

    &pira* bacteria: "0% !m in *en+th and $.%-$.1 !m in width

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    Structure of BacteriaStructure of Bacteria

    Particular structures

    capsule

    flagella 鞭毛

    pili菌毛

    spore 芽胞

    Essential structuresEssential structurescell wallcell wall

    细胞壁胞壁

    cell membranecell membrane细胞

    CytoplasmCytoplasm细胞质

    胞质

    nuclear materialnuclear material 核质

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    Gram +

    Gram -

    Cell wall

    Cell (inner) membrane Outer membrane

    Ribosomes

    Granule

    Cell wall

    NucleoidCell membrane

    Capsule

    Flagellum

    Pili

    Gram, C. 1884. Ueber die isolirteGram, C. 1884. Ueber die isolirteFarbung der Schizomyceten inFarbung der Schizomyceten in

    SchnittÄund Trocen!ra!araten.SchnittÄund Trocen!ra!araten.Fortschritte der MedicinFortschritte der Medicin, "ol. #, !ages, "ol. #, !ages

    1884:1884: Christian GramChristian Gram' First !ublication (or the Gram stain method)' First !ublication (or the Gram stain method)

    Editor's note: I would like to testify that I have found the Gram method to be one ofEditor's note: I would like to testify that I have found the Gram method to be one of

    the best and for many cases the best method which I have ever used for stainingthe best and for many cases the best method which I have ever used for staining

     Schizomycetes.Schizomycetes.

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    Cell wallCell wall

    &ituation:outmost portion.

    "-%$nm in

    thic)ness "$-

    2 of dr3wei+ht.

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    e wae wa  : ommon pep og ycanommon pep og ycanlayer layer 

     A backbone of N-acetyl glucosamine and N-acetylmuramic acid : Both discovered

    in Gram positive and Gram negative bacteria.

     A set of identical tetrapeptide side chain  attached to N-acetyl-muramic acid:

    different components and binding modes in Gram positive and Gram negative

    bacteria.

     A set of identical peptide cross bridges: only in Gram positive bacteria

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    Special components ofSpecial components of

    Gram positive cell wall Gram positive cell wall  Teichoic acid  

    &P4 / M P56789

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    ecial components of Gramecial components of Gram

    negative cell wall negative cell wall  

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    FunctionsFunctions of Cell Wall of Cell Wall Maintainin+ the ce**s characteristic shape- the ri+id

    wa** compensates for the f*exibi*it3 of the phospho*ipid membrane and )eeps the ce** fromassumin+ a spherica* shape

    ounterin+ the effects of osmotic pressure

    Pro,idin+ attachment sites for bacteriopha+es

    Pro,idin+ a ri+id p*atform for surface appenda+es-flagella fimbriae and pili a** emanate from thewa** and extend be3ond it

    P*a3 an essentia* ro*e in ce** di,ision

    e the sites of ma;or antigenic determinants of thece** surface。

    Resistance of ntibiotics 

    ll l f f

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    all!less forms ofall!less forms of

    "acteria "acteria ..

    *hen bacteria are treated +ith 1) enzymes that are lytic (or

    the cell +all e.g. lysozyme or #) antibiotics that inter(ere +ithbiosynthesis o( !e!tidoglycan, +all%less bacteria are o(ten!roduced.

    Usually these treatments generate non%iable organisms.

    *all%less bacteria that can not re!licate are re(erred to ass!hero!lasts -+hen an outer membrane is !resent) or!roto!lasts -i( an outer membrane is not !resent).

    ccasionally +all%less bacteria that can re!licate are

    generated by these treatments -/ (orms).

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    CellCell

    membranemembrane

    < !ite of bios"nthesis of #N$ cell wall pol"mers and membrane lipids% !electi&epermeabilit" and transport of solutes into cells

    < 'lectron transport and oidati&e phosphor"lation< 'cretion of h"drol"tic eoen"mes

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    MesosomesMesosomes

    • Mesosomes are specialized structuresformed by convoluted inveigh-nationsof cytoplasmic membrane, and dividedinto septal and lateral mesosome.

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    CytoplasmCytoplasm 

    omposed *ar+e*3 of water to+ether with proteins nuc*eic

    acid *ipids and sma** amount of su+ars and sa*ts

    Ribosomes: numerous "-2$nm in diameter with =$&>

    distributed throu+hout the c3top*asm> sensiti,e to

    streptom3cin and er3throm3cin site of protein s3nthesis

    Plasmids: extrachromosoma*

    +enetic e*ements

    Inclusions: sources of stored

    ener+3 e+ ,o*utin

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    Pla!idPla!id P*asmids aresma**, circu*ar/*ine, extrachromosoma*, doub*e-stranded D94 mo*ecu*es。 6he3are capab*e of se*f-rep*ication and contain

    +enes that confer some properties, such asantibiotic resistance, ,iru*ence factors。P*asmids are not essentia* for ce**u*ar

    sur,i,a*.  8nc*usions of8nc*usions of

    acteriaacteria

    *nclusions areaggregates of &ariouscompounds that arenormall" in&ol&ed instoring energ"reser&es or building

    blocs for the cell%*nclusions accumilatewhen a cell is grownin the presence ofecess nutrients andthe" are often

    obser&ed underlaborator"

    granulose

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    NucleusNucleus

    ?ac)in+ nuc*ear

    membrane absence

    of nuc*eo*i hence

    )nown as nuc*eicmateria* or nuc*eoid

    one to se,era* per

     bacterium.

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    Ca#sules and slime layersCa#sules and slime layers

    $hese are structures surrounding the outside of the cell envelo#e. $heyusually consist of #olysaccharide% however& in certain bacilli they arecom#osed of a #oly#e#tide #olyglutamic acid(. $hey are not essential tocell viability and some strains within a s#ecies will #roduce a ca#sule&

     whilst others do not. Ca#sules are often lost during in vitro culture.

    )ttachment

    *rotection from #hagocyticengulfment.

    +esistance to drying.

    ,e#ot for waste #roducts. +eservoir for certain

    nutrients.  #rotection

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    FlagellaFlagella 

    Monotrichate/4mphitrichate/?ophotrichate/Peritrichate 

    Identification

    of Bacteria Pathogenesis

    Motility of

    bacteria

    Some bacterial s#ecies are mobile and #ossesslocomotory organelles ! flagella. -lagella consist of anumber of #roteins including flagellin

    6he diameter of a f*a+e**um is thin 2$ nm and*on+ with some ha,in+ a *en+th "$ times the

    diameter of ce**. Due to their sma** diameterf*a+e**a cannot be seen in the *i+ht microscopeun*ess a specia* stain is app*ied. acteria can ha,eone or more f*a+e**a arran+ed in c*umps or spreada** o,er the ce**.

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    PiliPili

    *ili are hair!like #roections of the cell & $hey areknown to be rece#tors for certain bacterial viruses.

    Chemical nature is #ilin

    Classification and -unction

    a. ommon pi*i or fimbriae: fine ri+id numerous

    re*ated to bacteria* adhesion

     b. &ex pi*i: *on+er and coarser on*3 "-@ re*ated to

     bacteria* con;u+ation

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    'ndospores'ndospores

    (spores)(spores)

    < #ormant cell#ormant cell< Resistant to ad&erseResistant to ad&erse

    conditionsconditions

    - high temperatures- high temperatures

    - organic sol&ents- organic sol&ents

    < Produced when star&edProduced when star&ed< Contain calcium dipicolinateContain calcium dipicolinate

      #P$#P$ ##ipicolinic acidipicolinic acid

    <  Bacillus Bacillus andand ClostridiumClostridium

    8dentification of

    acteria

    Patho+enesis Aesistance

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    ,icroscope 

    ?i+ht Microscope 7*ectron Microscope

    Dar)fie*d Microscope

    Phase ontrast Microscope

    B*uorescence Microscope

    ofoca* Microscope)

    ,ethods

    !taining ,ethods

    &imp*e stainin+>Differentia* stainin+ C Gram

    stain 4cid-fast stain

    &pecia* stainin+C 9e+ati,e stain

    &pore stain B*a+e**a stain