mission impossible ii
TRANSCRIPT
The
mission ImpossibleII
JSTP 12
The
mission ImpossibleII
JSTP 12
The
mission
Impossible II
The toy story
Impossible
Themission
ImpossibleProject
โครง
โครง
โครงโครงงาน
โครงโครงงาน
โครงโครงงานProject
PROJECT = TOYGAME
FUN
PROJECT = TOYGAME
FUN
แบบฟอรมโครงงาน ทมาและความสำคญ วตถประสงค
ประโยชนทคาดวาจะไดรบ ตวแปรทเกยวของ
คมอการเลน
เลนอยางไรใหส
นก
คมอการเลน
เลนอยางไรใหส
นก
อานจบแลว จะสนกไหม
Every years someone has a great speech....
@#!$#%wee-tah-kah loo-loo
คนหจงบองตง
ตอยอด
ตอยอด
สรางยาลดอาการ คนหของFurby
Fin~
Innovation
What did we play ?
Detective
What did we play ?
Detective Created
What did we play ?
Detective Created Divas
What did we play ?
Detective Created Divas
Action
What did we play ?
Detective Created Divas
Business
Action
What did we play ?
Detective Created Divas
Impersonate
Business
Action
What did we play ?
Detective Created Divas
Impersonate
Business
Action
What did we play ?
ซอนแอบ ไขปรศนา
Detective Created Divas
Impersonate
Business
Action
What did we play ?
ซอนแอบ ไขปรศนา
เลน Lego พบจรวด หนยนต
Detective Created Divas
Impersonate
Business
Action
What did we play ?
ซอนแอบ ไขปรศนา
เลน Lego พบจรวด หนยนต
รองเพลง แตงตว
Detective Created Divas
Impersonate
Business
Action
What did we play ?
ซอนแอบ ไขปรศนา
เลน Lego พบจรวด หนยนต
รองเพลง แตงตว
เลนเกม แปลงราง
Detective Created Divas
Impersonate
Business
Action
What did we play ?
ซอนแอบ ไขปรศนา
เลน Lego พบจรวด หนยนต
รองเพลง แตงตว
เกมเศรษฐ เลนขายของ
เลนเกม แปลงราง
Detective Created Divas
Impersonate
Business
Action
What did we play ?
ซอนแอบ ไขปรศนา
เลน Lego พบจรวด หนยนต
รองเพลง แตงตว
บทบาทสมมต หมอรกษาคนไข
เกมเศรษฐ เลนขายของ
เลนเกม แปลงราง
P.P. TOYs
P.P. TOYs
P.P. TOYs
P.P. TOYs
P.P. TOYs
P.P. TOYs
Bacteria
BacteriaStyrofoam
Biodegradation
BacteriaStyrofoam
My project in academic style.
Styrofoam
Styrofoam
Styrene monomer
Polystyrene
Chemical formula is (C8H8)n
Monomer styrene
Thermoplastic
Blowing agents
Polystyrene
Chemical formula is (C8H8)n
Monomer styrene
Thermoplastic
Blowing agents
500 years++ for degradation
http://en.wikipedia.org/wiki/Polystyrene
Recycling & Incineration
Recycling & Incineration
1% turn back to polystyrene
most of the polystyrene is converted into carbon dioxide, water vapor, and heat.
"Ease of Disposal". Retrieved 2009-06-25
Photo by Napat Jaitui JSTP # 15
Styrene Monomer
Carbon Monoxide
Photo by Napat Jaitui JSTP # 15
Styrene Monomer
Carbon Monoxide
Photo by Napat Jaitui JSTP # 15
CARCINOGEN
cc
c cc
cc c
cc
c cc
cc c
Bacterianutrition‣ Energy source‣ Carbon source‣ Nitrogen source‣ Minerals‣Water‣ Growth factors
How can I find
the bacteria that able to
degrade a styrofoam?
SOIL
SOIL
SOILLandfill
Landfill foam
How can I find
the bacteria that able to
degrade a styrofoam?
How can I find
the bacteria that able to
degrade a styrofoam?
The ability
The key to isolate the effective microbe is the
degradability.
MSM Broth Bacteria selective broth
MSM Broth Bacteria selective broth
MSM broth‣K2HPO4
‣KH2PO4
‣(NH4)2SO4
‣MgSO4
‣ FeSO4.2HO2
‣MnCl2.4H2O‣CoCl2.6H2O‣CuCl2.2H2O‣NiCl2.6H2O‣Na2MoO4.2H2O‣ZnSO4.7H2O‣H3BO3
Sterile Styrofoam
MSM Broth Bacteria selective broth
MSM Broth Bacteria selective broth
Shake in shaker for 1 monththen inoculate to new freshbroth for sub culture.
Every week the solution in each flask was taken to the eppendorf then stored at 2C๐ for stop bacteria growth that use for monitor the changing of bacteria population.
MSM Broth Bacteria selective broth
MSM Broth Bacteria selective broth
MSM broth‣K2HPO4
‣KH2PO4
‣(NH4)2SO4
‣MgSO4
‣ FeSO4.2HO2
‣MnCl2.4H2O‣CoCl2.6H2O‣CuCl2.2H2O‣NiCl2.6H2O‣Na2MoO4.2H2O‣ZnSO4.7H2O‣H3BO3
Sterile Styrofoam
MSM Broth Bacteria selective broth
MSM Broth Bacteria selective broth
MSM Broth Bacteria selective broth
MSM Broth Bacteria selective broth
MSM Broth Bacteria selective broth
Foam in landfill Soil in landfill
Week
Week
WeekDominant
species
WeekDominant
speciesDiversity
Every week the solution in each flask was taken to the eppendorf then stored at 2C๐ for stop bacteria growth that use for monitor the changing of bacteria population.
DNA Replication : PCR (TopTaq Master Mix Kit)
16S rRNA gene Amplification by using Primer VR (Medlin et al., 1998) & VFC (Muyzer et al., 1993)
DNA Replication : PCR (TopTaq Master Mix Kit)
16S rRNA gene Amplification by using Primer VR (Medlin et al., 1998) & VFC (Muyzer et al., 1993)
DNA Replication : PCR (TopTaq Master Mix Kit)
16S rRNA gene Amplification by using Primer VR (Medlin et al., 1998) & VFC (Muyzer et al., 1993)
DGGE (Denature Gradient Gel Electrophoresis)
30% Urea + Formamine
60% Urea + Formamine
DGGE (Denature Gradient Gel Electrophoresis)
- 30% Urea + Formamine
60% Urea + Formamine
+
DGGE (Denature Gradient Gel Electrophoresis)
30% Urea + Formamine
60% Urea + Formamine
DGGE (Denature Gradient Gel Electrophoresis)
30% Urea + Formamine
60% Urea + Formamine
DGGE (Denature Gradient Gel Electrophoresis)
30% Urea + Formamine
60% Urea + Formamine
DGGE (Denature Gradient Gel Electrophoresis)
30% Urea + Formamine
60% Urea + Formamine
GC rich
DGGE (Denature Gradient Gel Electrophoresis)
30% Urea + Formamine
60% Urea + Formamine
GC low
GC rich
DGGE (Denature Gradient Gel Electrophoresis)
30% Urea + Formamine
60% Urea + Formamine
GC low
GC rich
Mar
ker
Soil
wee
k 1
Soil
wee
k 5
Soil
wee
k 6
Soil
wee
k 7
Soil
wee
k 8
Soil
wee
k 20
Foam
wee
k 1
Foam
wee
k 5
Foam
wee
k 6
Foam
wee
k 7
Foam
wee
k 8
Foam
wee
k 20
Con
trol
wee
k 6
Con
trol
wee
k 7
Con
trol
wee
k 8
Mar
ker
Mar
ker
Neg
ativ
e
Bacteria from foam Bacteria from soil Control
DGGE 26/04/55 Running time 300 minute from PCR product 24/04/55 template use 8 µl.
DGGE (Denature Gradient Gel Electrophoresis)
Mar
ker
Soil
wee
k 1
Soil
wee
k 5
Soil
wee
k 6
Soil
wee
k 7
Soil
wee
k 8
Soil
wee
k 20
Foam
wee
k 1
Foam
wee
k 5
Foam
wee
k 6
Foam
wee
k 7
Foam
wee
k 8
Foam
wee
k 20
Con
trol
wee
k 6
Con
trol
wee
k 7
Con
trol
wee
k 8
Mar
ker
Mar
ker
Neg
ativ
e
Bacteria from foam Bacteria from soil Control
DGGE 26/04/55 Running time 300 minute from PCR product 24/04/55 template use 8 µl.
DGGE (Denature Gradient Gel Electrophoresis)
Mar
ker
Soil
wee
k 1
Soil
wee
k 5
Soil
wee
k 6
Soil
wee
k 7
Soil
wee
k 8
Soil
wee
k 20
Foam
wee
k 1
Foam
wee
k 5
Foam
wee
k 6
Foam
wee
k 7
Foam
wee
k 8
Foam
wee
k 20
Con
trol
wee
k 6
Con
trol
wee
k 7
Con
trol
wee
k 8
Mar
ker
Mar
ker
Neg
ativ
e
Bacteria from foam Bacteria from soil Control
DGGE 26/04/55 Running time 300 minute from PCR product 24/04/55 template use 8 µl.
DGGE (Denature Gradient Gel Electrophoresis)
Mar
ker
Soil
wee
k 1
Soil
wee
k 5
Soil
wee
k 6
Soil
wee
k 7
Soil
wee
k 8
Soil
wee
k 20
Foam
wee
k 1
Foam
wee
k 5
Foam
wee
k 6
Foam
wee
k 7
Foam
wee
k 8
Foam
wee
k 20
Con
trol
wee
k 6
Con
trol
wee
k 7
Con
trol
wee
k 8
Mar
ker
Mar
ker
Neg
ativ
e
Bacteria from foam Bacteria from soil Control
DGGE 26/04/55 Running time 300 minute from PCR product 24/04/55 template use 8 µl.
DGGE (Denature Gradient Gel Electrophoresis)
Mar
ker
Soil
wee
k 1
Soil
wee
k 5
Soil
wee
k 6
Soil
wee
k 7
Soil
wee
k 8
Soil
wee
k 20
Foam
wee
k 1
Foam
wee
k 5
Foam
wee
k 6
Foam
wee
k 7
Foam
wee
k 8
Foam
wee
k 20
Con
trol
wee
k 6
Con
trol
wee
k 7
Con
trol
wee
k 8
Mar
ker
Mar
ker
Neg
ativ
e
Bacteria from foam Bacteria from soil Control
DGGE 26/04/55 Running time 300 minute from PCR product 24/04/55 template use 8 µl.
DGGE (Denature Gradient Gel Electrophoresis)
Mar
ker
Soil
wee
k 1
Soil
wee
k 5
Soil
wee
k 6
Soil
wee
k 7
Soil
wee
k 8
Soil
wee
k 20
Foam
wee
k 1
Foam
wee
k 5
Foam
wee
k 6
Foam
wee
k 7
Foam
wee
k 8
Foam
wee
k 20
Con
trol
wee
k 6
Con
trol
wee
k 7
Con
trol
wee
k 8
Mar
ker
Mar
ker
Neg
ativ
e
Bacteria from foam Bacteria from soil Control
DGGE 26/04/55 Running time 300 minute from PCR product 24/04/55 template use 8 µl.
DGGE (Denature Gradient Gel Electrophoresis)
The microscopic structure of Polystyrene observed by SEM
Pat Pataranutaporn1, Apinya.J2 Assistant prof. Savaporn Supaphol3, 1 PSU.Wittayanusorn school, 2Scientific Equipment Center
Prince of Songkla University 3Kasetsart University
Control : Polystyrene in MSM broth without bacterial source.
Regular polystyrene foam that didn’t use in experiment.
100x 200x 500x
The comparison of Polystyrene microscopic structure
Control
Regular polystyrene that didn’t use in experiment.
Control
Polystyrene in Medium with bacteria from foam sample.
100x 200x 500x
The comparison of Polystyrene microscopic structure
Regular polystyrene foam that didn’t use in experiment.Polystyrene in Medium with bacteria from foam sample.
Bacteria from foam
Polystyrene in Medium with bacteria from foam sample.
100x 200x 500x
The comparison of Polystyrene microscopic structure
Regular polystyrene foam that didn’t use in experiment.
Bacteria from foam
Polystyrene in Medium with bacteria from soil sample.
100x 200x 500x
The comparison of Polystyrene microscopic structure
Regular polystyrene foam that didn’t use in experiment.
Bacteria from soil
Polystyrene in Medium with bacteria from soil sample.
100x 200x 500x
The comparison of Polystyrene microscopic structure
Regular polystyrene foam that didn’t use in experiment.Polystyrene in Medium with bacteria from soil sample.
Bacteria from soil
Polystyrene in Medium with bacteria from soil sample.
100x 200x 500x
The comparison of Polystyrene microscopic structure
Regular polystyrene foam that didn’t use in experiment.Polystyrene in Medium with bacteria from soil sample.
Bacteria from soil
Polystyrene in Medium with bacteria from soil sample.
100x 200x 500x
The comparison of Polystyrene microscopic structure
Regular polystyrene foam that didn’t use in experiment.Polystyrene in Medium with bacteria from soil sample.
Bacteria from soil
Soil
wee
k 1
Soil
wee
k 5
Soil
wee
k 6
Soil
wee
k 7
Soil
wee
k 8
Foam
wee
k 1
Foam
wee
k 5
Foam
wee
k 6
Foam
wee
k 7
Foam
wee
k 8
Con
trol
wee
k 6
Con
trol
wee
k 7
Con
trol
wee
k 8
Foam sampleSoil sampleControl
Soil
wee
k 1
Soil
wee
k 5
Soil
wee
k 6
Soil
wee
k 7
Soil
wee
k 8
Foam
wee
k 1
Foam
wee
k 5
Foam
wee
k 6
Foam
wee
k 7
Foam
wee
k 8
Con
trol
wee
k 6
Con
trol
wee
k 7
Con
trol
wee
k 8
Soil
wee
k 1
Soil
wee
k 5
Soil
wee
k 6
Soil
wee
k 7
Soil
wee
k 8
Foam
wee
k 1
Foam
wee
k 5
Foam
wee
k 6
Foam
wee
k 7
Foam
wee
k 8
Con
trol
wee
k 6
Con
trol
wee
k 7
Con
trol
wee
k 8
Foam sampleSoil sampleControl
Soil
wee
k 1
Soil
wee
k 5
Soil
wee
k 6
Soil
wee
k 7
Soil
wee
k 8
Foam
wee
k 1
Foam
wee
k 5
Foam
wee
k 6
Foam
wee
k 7
Foam
wee
k 8
Con
trol
wee
k 6
Con
trol
wee
k 7
Con
trol
wee
k 8
Soil
wee
k 1
Soil
wee
k 5
Soil
wee
k 6
Soil
wee
k 7
Soil
wee
k 8
Foam
wee
k 1
Foam
wee
k 5
Foam
wee
k 6
Foam
wee
k 7
Foam
wee
k 8
Con
trol
wee
k 6
Con
trol
wee
k 7
Con
trol
wee
k 8
Foam sampleSoil sampleControl
Soil
wee
k 1
Soil
wee
k 5
Soil
wee
k 6
Soil
wee
k 7
Soil
wee
k 8
Foam
wee
k 1
Foam
wee
k 5
Foam
wee
k 6
Foam
wee
k 7
Foam
wee
k 8
Con
trol
wee
k 6
Con
trol
wee
k 7
Con
trol
wee
k 8
Soil
wee
k 1
Soil
wee
k 5
Soil
wee
k 6
Soil
wee
k 7
Soil
wee
k 8
Foam
wee
k 1
Foam
wee
k 5
Foam
wee
k 6
Foam
wee
k 7
Foam
wee
k 8
Con
trol
wee
k 6
Con
trol
wee
k 7
Con
trol
wee
k 8
Foam sampleSoil sampleControl
Molecular cloning DNA isolation & DNA Analyzing
Pat Pataranutaporn1, Sureeporn Nualkaew2, Prof. Dr. Amornrat Phongdara2 1 PSU.Wittayanusorn school, 2 Prince of Songkla University
Mar
ker
Soil
wee
k 1
Soil
wee
k 5
Soil
wee
k 6
Soil
wee
k 7
Soil
wee
k 8
Soil
wee
k 20
Foam
wee
k 1
Foam
wee
k 5
Foam
wee
k 6
Foam
wee
k 7
Foam
wee
k 8
Foam
wee
k 20
Con
trol
wee
k 6
Con
trol
wee
k 7
Con
trol
wee
k 8
Mar
ker
Mar
ker
Neg
ativ
e
Bacteria from foam Bacteria from soil Control
DGGE 26/04/55 Running time 300 minute from PCR product 24/04/55 template use 8 µl.
DGGE (Denature Gradient Gel Electrophoresis)
Mar
ker
Soil
wee
k 1
Soil
wee
k 5
Soil
wee
k 6
Soil
wee
k 7
Soil
wee
k 8
Soil
wee
k 20
Foam
wee
k 1
Foam
wee
k 5
Foam
wee
k 6
Foam
wee
k 7
Foam
wee
k 8
Foam
wee
k 20
Con
trol
wee
k 6
Con
trol
wee
k 7
Con
trol
wee
k 8
Mar
ker
Mar
ker
Neg
ativ
e
Bacteria from foam Bacteria from soil Control
DGGE 26/04/55 Running time 300 minute from PCR product 24/04/55 template use 8 µl.
DGGE (Denature Gradient Gel Electrophoresis)
Mar
ker
Soil
wee
k 1
Soil
wee
k 5
Soil
wee
k 6
Soil
wee
k 7
Soil
wee
k 8
Soil
wee
k 20
Foam
wee
k 1
Foam
wee
k 5
Foam
wee
k 6
Foam
wee
k 7
Foam
wee
k 8
Foam
wee
k 20
Con
trol
wee
k 6
Con
trol
wee
k 7
Con
trol
wee
k 8
Mar
ker
Mar
ker
Neg
ativ
e
Bacteria from foam Bacteria from soil Control
DGGE 26/04/55 Running time 300 minute from PCR product 24/04/55 template use 8 µl.
DGGE (Denature Gradient Gel Electrophoresis)
Hello Who are you ?
Molecular cloning Despicable Me: Minion Mayhem
PCR Product
PCR Product
PCR Product
Mix DNA for ligation
pGEM- T easy
Target DNA
PCR Product
Mix DNA for ligation
PCR Product
Mix DNA for ligation
Transform plasmid to the competent cell.
E.Coli as
Transform plasmid to the competent cell.
Transform plasmid to the competent cell.
Transform plasmid to the competent cell.
Transform plasmid to the competent cell.
Transform plasmid to the competent cell.
The separate DNA
Mar
ker
Soil
wee
k 1
Soil
wee
k 5
Soil
wee
k 6
Soil
wee
k 7
Soil
wee
k 8
Soil
wee
k 20
Foam
wee
k 1
Foam
wee
k 5
Foam
wee
k 6
Foam
wee
k 7
Foam
wee
k 8
Foam
wee
k 20
Con
trol
wee
k 6
Con
trol
wee
k 7
Con
trol
wee
k 8
Mar
ker
Mar
ker
Neg
ativ
e
Bacteria from foam Bacteria from soil Control
DGGE 26/04/55 Running time 300 minute from PCR product 24/04/55 template use 8 µl.
DGGE (Denature Gradient Gel Electrophoresis)
ElectropherogramCode name : Control 4
Code name : Control 4
Basic Local Alignment Search Tool (BLAST)
Database Name TL/16S_ribosomal_RNA_Bacteria_and_Archaea Description 16S ribosomal RNA sequences (Bacteria and Archaea) Program BLASTN 2.2.27+ Molecule type nucleic acid Query Length 1055
Code name : Control 4
Basic Local Alignment Search Tool (BLAST)
Database Name TL/16S_ribosomal_RNA_Bacteria_and_Archaea Description 16S ribosomal RNA sequences (Bacteria and Archaea) Program BLASTN 2.2.27+ Molecule type nucleic acid Query Length 1055
Code name : Control 4Phylogenetic tree
Code name : Control 4Phylogenetic tree
Code name : Control 4Phylogenetic tree
ElectropherogramCode name : Control 7
Code name : Control 7
Basic Local Alignment Search Tool (BLAST)
Database Name TL/16S_ribosomal_RNA_Bacteria_and_Archaea Description 16S ribosomal RNA sequences (Bacteria and Archaea) Program BLASTN 2.2.27+ Molecule type nucleic acid Query Length 1006
Code name : Control 7
Basic Local Alignment Search Tool (BLAST)
Database Name TL/16S_ribosomal_RNA_Bacteria_and_Archaea Description 16S ribosomal RNA sequences (Bacteria and Archaea) Program BLASTN 2.2.27+ Molecule type nucleic acid Query Length 1006
Code name : Control 7Phylogenetic tree
Code name : Control 7Phylogenetic tree
Code name : Control 7Phylogenetic tree
Code name : Fe5
Bacterial plating Plate streaking & Plate spreading
Pat Pataranutaporn1, Panwong Kuntanawat2 1 PSU.Wittayanusorn school, 2 King Mongkut's University of Technology Thonburi
Bacterial plating on MSM & MSM + PSA agar cultured at 37oC over 48 hr.
Bacterial plating on MSM & MSM + PSA agar cultured at 37oC over 48 hr.
Bacterial plating on MSM & MSM + PSA agar cultured at 37oC over 48 hr.
Polystyrene-coacrylic acid (PSA)(particles diameter 500 nm)
MSM Agar
Bacterial plating on MSM & MSM + PSA agar cultured at 37oC over 48 hr.
Polystyrene-coacrylic acid (PSA)(particles diameter 500 nm)
MSM Agar
Polysaccharide
Cx(H2O)y
Bacterial plating on MSM & MSM + PSA agar cultured at 37oC over 48 hr.
Bacterial plating on MSM & MSM + PSA agar cultured at 37oC over 48 hr.
Bacterial plating on MSM & MSM + PSA agar cultured at 37oC over 48 hr.
Bacterial plating on MSM & MSM + PSA agar cultured at 37oC over 48 hr.
Research Achievements
Research Achievements
Research Achievements
13th NCSC, Jaipur India 2011
Youth summit 2012, Dubai UAE
JSTP Scholarship
STT 36
BYEE, Leverkuzen Germany
BYEE Poster Prize from india
Publication & media
JSTPMedia www.jstpmedia.org
Biodegradation of Polystyrene Foam by the Microorganisms
from Landfill
P.P. TOYs
P.P. TOYs
หนงตะลง
หนงตะลงWEB app
หนงตะลงWEB appCulture
Developed in SWF format http://jstpmedia.org/images/complete.swf
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JSTP 15/3
P.P. TOYs
P.P. TOYs
Space
SpaceGravity
Space
EnzymeGravity
JAXA
v
v
The Evaluation of Amylase Activity under Microgravity
By JSTP 12 Pat Pataranutaporn Pondet Ananchai Arnan Schuett
ChemistryBiotechnology Electronic
Research Team
JSTP 12
ChemistryBiotechnology Electronic
Research Team
JSTP 12The youngest team ever!
Possibility of Enzyme
Possibility of Enzyme
Collision Theory
Possibility of Enzyme
Collision Theory‣Enzyme Concentration‣Substrate Concentration‣Inhibitors‣Temperature‣pH
Gravity
GravityFree motion of molecule
Salivary stress markers and psychological stress in simulated microgravity: 21 days in 6° head-down tilt.
Rai B, Kaur J. Catholic University Leuven, Belgium.
Spaceflight occurs in an environment of temperature extremes, microgravity, solar and galactic cosmic radiation, lack of atmospheric pressure, and high-speed micrometeorites. Exposure to microgravity and the space environment during space missions of short and long duration has important medical and health implications for astronauts. Psychological well-being is of increasing importance in planned spaceflights and interplanetary missions of long duration. The 6° head-down tilt (HDT) is an established method of mimicking low gravity on earth. The aim of the present study was to determine the effects of 21 days of HDT on psychological stress in 12 healthy male volunteers.
Psychological state was assessed by the current stress test, and chromogranin-A (CgA), cortisol, alpha-amylase, and beta-endorphin were measured in saliva. After one week of HDT, all volunteers developed psychological stress, and secretion of CgA, cortisol, alpha-amylase, and beta-endorphin were all significantly higher. Thus, 6° HDT appears to be a valid model to induce psychological stress changes in the immune system, changes that might also be encountered by astronauts and cosmonauts during both a short stay in space, such as that required while orbiting a space station, and in longer spaceflights.
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Difference enzyme activity rate affected by gravity
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