Bio notes for your ib survival game
Bio notes for your ib survival game
A2.3.2 Features ommon to viius: All are intercellular parasites, all are small
qll are Foxed insize,no grouwth or developmert, all use nucieic aid os the genehc
all have material.
All have a capsd made of protein. None have cutoplasm
no or fY very few enzymes
Vinuses vanyin: Range of size,ONNor RNA, 000bte or sinqle stranded,citesas
-At.2
A2.3.5 Crigin of viruses : Proaressive hyctess eqressive hyothesis
Prgressive hypothesis states that viruses arose by taking and modifying ell
Components. EVidence: retroviruses
The regressive hypothesis Viruses-arose by lpoPg loss of cellular compon ens.
Pracice Problem 3
Amoeba drawn at 200x life si2e. Find the actual size of
Tmage Size: 19.S-lcm = IG.Scm the amoeba
cOnyert to mm= G.S 0 ISS mm
IGSmm 0.82SMm
200X
A2.2.3Develspments in microSCoy
Magnification i how much largor an object appears comed
to its real size.
Genetits of a compourd light microscope
E05e of use,less expensive to buy, con otb serve dead or livig
cells in color, Cell movement con be studied , quick specinen
preparation (minutes o haurs no need for high volkgo de chicity.
Umitahions: maximum magnificahion of ahout is00x
(ow resolying power (o.2Ssm to 0.3 um)
Indirect active transport or cotransport, where the Movement of one solue
down is concentra hon arodient dr yes the movement of thesecand solute
against is concenira hon gradrent.
Processes of We in unicellslar organisms: MRHMGREN
metobolism : chemical reacHOns that toke ploce within a cel.
-response to shmui i reaChng to hanges in the externalen iron ment
homeostasis: the maintanence of Constant inteInal cond1hons, desp1te
Chang es to their external environmenis.
movement living things have some control over their place and posihon
9rowhi cells can inctease in size Over a period of hme
reproduchbn i heproduchon ofofspring
excrehon i removal of metabolic waste produc
nutihoh : intake or produchon of nutiens
ellwall
plant cel
erdoplasmc rehculum
Vacuole
mitochondia
nucleus
plasma mernbrane
chlarop last
qogbody
nbosomes
cytoplaSm.
endoplasmic
rehculum
animal cell
ve
sicle
mtochondria
nbosomes
innermenbrane
nudeus.
Mitochondria Ouermembrane
Lerdplamic
refedum
hscfear
membrane
Cristae pofe double
matri
chromahin
,doutkemembrane
Chloroplast
20srihosome
-DNA Snoath
thytalkoid (grenndm s Mde ty) tndaplae
grannum rehialyn
stromamellu
Vacaole
tonopl<t
nbosomes
cel
sap
Roughendoplasmie
rehialen
aotgi appora us
vesicles
Flagela Cha
Ales
nuedeus
VE
Unele
cyfopteasn iw
Cel wall
Vacusle
L(eatidles
A2.2.6 Eukaryotic cell Structure common suchures
nucleus, free and bound 8os nbosomes, Rough erdoplasrmic rehculum
Smooth endoplasmic rehculum, golgi apparakus, vesicles,luposome,
mitochondria chloro plast vacuole microtubules and centrioles cytoskelton
cilia and flagella.
cutoplosm
Golgi
bodies
y sosome !! Struchured diagom
of an eukanyotic cer
Srooth ER
Vacuole
Plasma membrane Prokaryotes : Archaea, Bactesia
Ouclear Eukaryofes : animal plants, Rungi
membrae ucleod A2.2.5
centriole Structuces of a prokaryotC cell
CellCplasmo membrane)
cytoplasm ibosome, cell wall, pli
Prokaryohc cell ONA íS naked,which means capsule , fla gellum
that the DNA is not asso cíated with proteins
Plqshds :onlyin plant cel! Vacuoles: animal cell,fungi celland plant cell
Centrioles: aniMat ceI and Plant cel
cell wall : Plant and Pungi cell
cilia and Plaqetta : animal and plont cell
"Encdo symbiosi's
42.2.12 Origin of eukaryohc cels by endosym brosis symbiosis is an interacton
O infolding cf the prokaryotic cel membrane between to different organisms
living in close physical associahon
cndosymbiosís typically to the advantage in both.
.în endosymbiosis, one cell ived
within the other and 6ecame increa singly interdependent
until the unt could only exist as a whole.
A2.2.4 Aypical cellstruckure in eukaryotes
Red blood cel : no nucleus, tes Aseptate Fungal Hyphae: many nucler
Skeletal muscles: multinucleated
Phloem sieve tube elementi lOses heir nucleus, anucleated
ReVSion village: state hue main Outline why viruses ore nof regarded
as Iwing organ1sm: lack cellular struchureS,unable to carry cut meta boliz
reachns
eh
MicroscopY metre, milhinetre, mIcroMeenanometre
SI units: lm = lo00Mn (lo) 00:IOo (I0 I00: IO00 loOo(109)
m > mm (multiply by lo0o) 4nanometre (nm) to one
micronetre
m> pm (muliply by l000:2 times)
m nm (mulhiply by l0003 times ) 1nm to one mm I00 O.000OoI
+ l000
Anm to 1m =
(io79)
= O.00O0000I
m
C101)
IO0cm= (0Omm
X\00o x\000
lowest solute
Concentraion 8: Hypotonic 2% suqar
c Hypertonic 4o sugar
A2.3.3
Gocteriophgqe Lamda they are obligate intercellular viruses
hat speiticalls infect bacteria,.
Bacteniophage lamda con utlise both lyic and lysogenic cycles.
A2.3.9 Lysogenic cycle: the vinUs assimilates its qenome within he host
cel's genome to achieve eplicahion without killing the host.
Lytic cyde: The vicus reproduces and bursts out of the host cel, killing it
ysogenic cycde: O Phage atachmernt to host cel:the phage must atach
itself to a eceptor proten.
Phage oNA entry into hcst cell genehic
many phages
matenial.
haye atube for delivering
S Phage DNA Ís integrated iato hoat qenome After integrakon the virus only
exisis as alength of ONA within a kacterial qenome.
@ONA roplicaton In this stage the virus iS called a prophogs.
cell dËvision
utic cycle: if a, bachenium containing prophage ís exposed to strssors
Such as Uy light low nutrient Conditions Or chemicals, prophage
extract themselves from the host qenome and enter Hhe lytc cycle.
Lyic cycie: Phage atachment to host cell Assembly of new phage
viruses
ha ge DNA erntry into host cell ysis andspread.
a Phage ONA eplicahon
@hage prokein syn thesis The host cl's RNA polymerase is used to trarscribe
Phage ONA into phage RNA
the host cell's nbosomes are used to translate phaqe RNA into phage proteins.