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Heredity
—Variation
—genotype
Variationphenotype
VariationMorphological
VariationBacteriaL
form
bacteriaL
FormVariationStructure
Variation
(1)CapsuleCulture
mediumLose
of
capsuleMouseSpore40℃
~
42
℃lose
of
Spore10~20dStructure
Variation(2)0.1%
carbolic
acidlose
of
FlagellaOFlagellaHColony
shape
VariationSmooth
colonyRough
colonyThis
variation
always
follow
somevariation
of
other
charactervirulence
VariationBovine
tuberclebacillus13
yearsBCG230
generationsvirulence
VariationDiphtheria
bacilliWithout
virulenceGaining
virulenceLysogenic
conversionresistance
VariationStaphylococcus
>90%PNCDysentery
bacteria
(Sensitive
Strain)S.M.Resistant
StrainS.M
dependent.
(SD).Bacterial
genetic
material
is
DNA.
DNA
is
tobe
carrier
of
gene
and
carryvariousgeneticinformation.Bacterial
genetic
information
islocatedgenome,
it
include
chromosome
and
geneticmaterial
which
locate
outside
ofchromosome.I.
Chromosomeclosed
double-Strandedcircular
DNA
moleculesCharacter1、Single
copy
sequences,repeat
sequences
is
less
2、Function
dependence
gene
concentrate
to
operon3、Having
continuous
gene,
no
intron4、Its
amount
depend
on
its
growth
conditions5
、Bidirectional
replicationPathogenicity
island (
PAI
)--
位于致病菌染色體上-- 常為分子量較大(20~100kbp)的基因群-- 攜帶毒力相關(guān)基因的外源性DNA片斷--
兩側(cè)往往含有重復(fù)序列或插入序列-- 其G+C%與密碼使用與宿主菌染色體有明顯差異II.
PlasmidPlasmids
are
small,
circular/line
,extra-chromosomal
,double-stranded
DNAmolecules;
They
are
capable
of
self-replicationand
contain
genes
that
confer
some
properties,such
asantibioticresistance
,virulencefactors
;They
are
not
essential
for
cellular
survival.Transfer
propertiesConjugative
plasmids;Non-conjugative
plasmidsPhenotypic
effectsF
factor;Col
plasmids;R
factor;Vi
plasmidCopy
NumbersStringent
plasmid;Relaxed
plasmidsCompatibilityCompatibility
plasmid;Incompatibility
plasmidsClassification
of
PlasmidsIII. Bacteriophage
(phage)1.
Definition--- viruses
that
infect
bacteria,
fungi,spirichaete
et
al.---
obligate
intracellular
parasites--- being
highly
host-specific--- being
a
type
of
bacterial
genetic
materials--- Virulent
phageand
Temperate
phage2. Properties
of
phageMorphologyUnit
of
measurement --- nm
;
Visible
with
EMDifferent
sizes
and
shapesStructureHeadTailCompositionNucleic
acid:
either
DNAor
RNA
but
not
bothds
DNA,
ss
RNA,
ss
DNAencode
3-5
gene
productsto
over
100
gene
productsProtein:
function
ininfection
and
protect
thenucleic
acidRelation
between
host
cell
and
phageLytic
or
Virulent
PhagesDefinition:Lytic
or
virulent
phages
are
phageswhich
can
only
multiply
in
bacteria
and
killthecellbylysisat
theendofthelife
cycle.Lytic
CycleAdsorptionPenetrationBiological
SynthesisMaturation
and
ReleaseAdsorptionPenetrationBiological
SynthesisMaturation
andReleaseLytic
cyclenormalbacteriophageBacteriophagebinding
to
andinjecting
theirDNA
into
abacterial
cellPlaquePhenomenon
of
lytic
bacteriaPlaque熒光假單胞菌Assay
for
Lytic
PhageLytic
phage
are
enumerated
by
a
plaque
assay.噬菌斑測定A
plaqueisaclear
areawhichresultsfrom
thelysis
of
bacteria.A
plaque
arises
from
a
single
infectious
phage,
itis
called
a
pfu
(plaque
formingunit).2) Lysogenic
or
Temperate
PhageThe
phage
DNA
actually
integrates
into
the
hostchromosome
and
is
replicated
along
with
thehost
chromosomeandpassed
ontothedaughtercells.This
phage
can
enter
a
quiescent
state
in
the
cell.
In
thisquiescent
state
most
of
the
phage
genes
are
not
transcribed;the
phage
genome
exists
in
a
repressed
state.The
phage
DNA
integrated
into
the
host
chromosome
iscalled
a
prophage
because
it
is
not
a
phage
but
it
has
thepotential
to
produce
phage.The
cell
harboring
a
prophage
is
termed
a
lysogenicbacterium.AdsorptionPenetrationProphageFormationLysogenic
bacteriumLysogenic phage
can
either
enter
a
quiescent
state
in
thecell
or
multiply
via
the
lytic
cycle.It
posses
a
potential
to
produce
daughter
phage
andsplitting
bacterium.InductionReplicationMaturation
andReleaseUsed
in
treatment
of
bacterial
infectionsUsed
for
the
identification
of
pathogenicbacteria
(phage
typing
噬菌體型分型)Used
in
molecular
biology4. Application
of
phageTransposon,TnMu
phage--- jumping
genes
or
movable
genes--- Insertion
sequence,
ISTransposaseABCDEFG
GFEDCBAISISISISResistanceGene(s)ResistanceGene(s)IV. Transposable
elementInsertion
sequences
(IS)Being
transposable
genetic
elements
that
carry
noknown
genes
except
those
that
are
required
fortranspositionSmall
stretches
of
DNA
that
have
at
their
ends
repeatedsequences.
Between
the
terminal
repeated
sequencesthere
are
sequences
that
can
control
transposition
butno
other
nonessential
genes
are
present.TransposaseABCDEFG
GFEDCBATransposons
(Tn)
Being
transposable
genetic
elements
that
carry
one
or
moreother
genes
in
addition
to
those
which
are
essential
fortranspositionIts
structure
is
similar
to
IS.The
extra
genes
are
locatedbetween
the
terminal
repeated
sequences.Many
antibiotic
resistance
genes
are
located
on
transposons.,these
antibiotic
resistance
transposons
are
a
major
factor
inthe
development
of
multiple
drug
resistance.ISISISISResistanceGene(s)ResistanceGene(s)Type
of
TransposonComposite
Transposon IS
+resistancegene+
ISComplex
Transposonrepeat
sequence(30-40bp)+
resistance
gene
andtransposition
gene
+
repeat
sequence(30-40bp)Transposition
MechanismNon-replicativetranspositionReplicative
transpositionConjugative
transposition一種運(yùn)動性的DNA分子,具有獨(dú)特結(jié)構(gòu)可捕獲和整合外源性基因,使之轉(zhuǎn)化為功能性基因的表達(dá)單位??纱嬖谟谌旧w、質(zhì)?;蜣D(zhuǎn)座子上,是細(xì)菌固有的遺傳單位。integron
-gene
cassettes
systemV. Integron(In)5’3’intIgene1Structure
ofInattI
gene2A
B
CP5′3′geneRYYYAACGTTRRRYattCattC3¢CS5¢CSVariable
regionP2P1gene
cassettes5¢CS
intI
geneEncode
integrase,catalyze
integrationbetween
gene
cassettes
and
shorthomology
Integration
Site
of
exogenous
gene
Priming
regionsequence
(attI
or
attC)According
intI
gene,
In
can
be
divide
6
groupPromotor
of
integrasePromotor
of
V-regionGene
cassettes基因盒
Small
movable
DNA,Only
phore
ageneand
a
specific
recombination
site(attC),having
no
promotor
Itsgene
cassettes
carry
resistancegenemostly
3
open
reading
frameqacED1 編碼季胺類化合物耐藥性sul1 編碼磺胺類藥物耐藥性O(shè)RF5 功能不明3¢CSI.
Mutation1.
Type--- spontaneous
mutation
and
induced
mutation--- point
mutation
and
chromosomeaberration2.
Mechanism--- substitution
(transition
and
transversion)--- deletion
or
insertion---
rearrangement3.
CharacterWild
strainMutant
strain--- occur
with
a
frequency
of
10-9~10-6
,but
can
be
induced
by
artificialstimuli--- posses
spontaneityand
random--- reverse
mutationII Gene
transfer
and
recombinationGene
transfer
and
recombination
is
mainreason
of
bacterium
producing
various
genecombination
to
fit
environment
in
short
time.The
finish
of
this
process
need
donor
cell,recipient
cell
and
carrier.1.
TransformationRecipient
cellDonor
cell
Cell-free
DNAdirect
uptakeCondition
of
transformationThecompetence
ofrecipient
cellConfiguration,
purity
and concentration
of
DNADouble-stranded
DNARestriction-enzymesystem
and
other
nuclease
ofrecipient
cellEnvironment
condition,
such
as
temperature,pHPreparation
of
competence
cell---
The
competence
always
in
the
end
of
growth
cycle---
Its
length
of
time
dependent
on
strains---
Treatment
with
Calcium
chloride
and
temperature
shock2.
ConjugationDonorcellRecipientcellSex
piliConjugative
PlasmidCharacter--- Donor
cell
can
carry
genes
coding
sexpilus--- Contactofthetwocells
directlyPhysiologicalStatesofF
FactorF+F+HfrHigh
frequency
of
recombinationF+HfrPhysiologicalStatesofF
FactorF’Hfr
F’MethodF+
ⅹ
F-F+Hfr
ⅹ
F-F-F’
plasmidR
plasmidF+F-F+F-F+F+F+F+DonorRecipient1)
F+
ⅹ F
-
2F+-- high
transfer
of
donor
F
factor2) Hfr
ⅹ F
-F-HfrF-HfrF-HfrF-HfrF--- F-
rarely
becomes
Hfr
while
Hfr
remains
Hfr-- High
transfer
of
certain
donor
chromosomal
genesF’F’F’F’F’F-F’F-3)
F’
ⅹ F
-
2F’-- F-
becomes
F’
while
F’
remains
F’-- High
transfer
of
donor
genes
on
F’4)
RPlasmid---
component
ofRTF(coding
sex
pili)Resistance
determinant---
relate
with
mutipleantibiotic
resistanceRTFR
determinant3.
TransductionDonorcellcellPlasmid
or
chromosome
DNA
RecipientBacteriophageGeneralized
transductionRestricted
transduction1) Generalized
transduction--- Occurs
in
the
end
of
lytic
cycle--- Caused
by
assembly
mistake--- any
of
donor
genetic
information
transfer
tothe
chromosome
of
recipientGeneralized
transduction2) Restricted
transduction--- Occurs
in
the
end
of
lysogenic
cycle--- Caused
by
drop
mistake--- some
certain
donor
genetic
information
can
transfer
tothe
chromosome
of
recipientRestricted
transductiongalbiogalbiogalbiogalbiobio4. ly
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