Shikimic acid is an important biochemical metabolite found in plants and microorganisms. It was first isolated from the Japanese star anise plant in 1885. The shikimate pathway is a seven step metabolic route used by plants and microbes to synthesize the aromatic amino acids phenylalanine, tyrosine, and tryptophan. This pathway is not present in animals. Shikimic acid is the starting point for the biosynthesis of many important phenolic compounds like flavonoids, tannins, lignin, and gallic acid. It is also a precursor for indole derivatives and the psychedelic compound DMT. Glyphosate herbicide works by inhibiting the shikimate pathway in plants
Flavonoids classification, isolation and identificationMona Ismail
Flavonoids are groups of polyphenolic compounds which are found in fruits, flowers, seeds & vegetable.
(named from the Latin word flavus meaning yellow, their colour in nature)
1) BASED ON THE CHEMICAL NATURE OF NON SUGAR MOIETY
2) BASED ON TE NATURE OF SUGAR MOITY
3) BASED ON LINKAGE BETWEEN GLYCON AND AGLYCON PORTION
4) BASED ON THERAPEUTIC NATURE OF GLYCOSIDE
Utilization of radioactive isotopes in the investigation of biogenetic studiesMs. Pooja Bhandare
Isotopes: TWO TYPES OF ISOTOPES,Radioactive isotopes.
Stable isotopes, Radiolabelled Tracers ( Radiolabelled compounds), Radiotracer Technique, Steps in Tracer Technique,
Selection of Radioisotopes.
Preparation of Radioisotopes.
Introduction/Insertion of Radiolabelled compound in biological system (Plant part) Seperation and determination of labelled compound in various biochemical reaction, Preparation of labelled compounds : Insertion of Radiolabelled compound in plant part, Root feeding, Stem feeding, Direct Injection, Floating Methods, Spray technique, Separation or Isolation of Radiolabelled compound and detection of radioisotope labelled compound. Detection and assay of Radioactive labelled compound, Detector system used (Analysis of Isotopic content). Method in Tracer Technique,
Precursor – Product sequence
Double and Multiple Labelling
. Competitive Feeding,Sequential Analysis
Applications of Tracer Technique
Medicinal chemistry 5 semester all synthesis Anjali Bhardwaj
Learn All
Medicinal Chemistry synthesis of
B.Pharmacy 5th Semester
As per PCI Syllabus
List Of Drug synthesis as per PCI Syllabus for B.Pharmacy 5th Semester
-Diphenhydramine hydrochloride -Furosemide
-Triprolidine hydrochloride -Methyldopate hydrochloride
-Promethazine hydrochloride -Disopyramide phosphate
-Cimetidine -Warfarin
-Meclorethamine -Tolbutamide
-Mercaptopurine -Benzocaine
-Methotrexate -Procaine
-Nitroglycerin -Dibucaine
-Isosorbide dinitrite
-Acetazolamide
-Chlorthiazide
Shikimic acid pathway is "metabolic pathway. "
,means metabolites are organic compounds synthesized by plant using enzyme mediated chemical reactions called metabolic pathway .
Now the metabolites are two types primary and secondary metabolites. The shikimic acid pathway is biosynthesis of secondary metabolites of phenylalanine, tyrosine and tryptophan(amino acid).
Glycosides play numerous important roles in living organisms. Many plants store chemicals in the form of inactive glycosides. These can be activated by enzyme hydrolysis, which causes the sugar part to be broken off, making the chemical available for use. Many such plant glycosides are used as medications. In animals and humans, poisons are often bound to sugar molecules as part of their elimination from the body.A glycoside is a molecule consisting of a sugar and a non-sugar group, called an aglycone. The sugar group is known as the glycone and can consist of a single sugar group or several sugar groups. The sugars is in its cyclic form and is covalently attached to the aglycon through the hydroxyl group of the hemiactal function.
There are many different kinds of aglycones. It can be a terpene, a flavonoid, a coumarin or practically any other natural occurring product (se figure 1)
The glycone can be attached to the aglycon in many different ways. The most common bridging atom is oxygen (O-glycoside), but it can also be sulphur (S-glycoside), nitrogen (N-glycoside) or carbon (C-glycoside). In general, one distinguishes between α-Glycosides and β-glycosides, depending on the configuration of the hemiactal hydroxyl group. The majority of the naturally occurring glycosides are β-glycosidesGenerally glycosides are more polar than the aglycones and as a result glycoside formation usually increases water solubility. This may allow the producing organism to transport and store the glycoside more efficiently
Many biologically active compounds are glycosides. The pharmacological effects are largely determined by the structure of the aglycone.
Glycosides comprise several important classes of compounds such as hormones, sweeteners, alkaloids, flavonoids and antibiotics
Flavonoids classification, isolation and identificationMona Ismail
Flavonoids are groups of polyphenolic compounds which are found in fruits, flowers, seeds & vegetable.
(named from the Latin word flavus meaning yellow, their colour in nature)
1) BASED ON THE CHEMICAL NATURE OF NON SUGAR MOIETY
2) BASED ON TE NATURE OF SUGAR MOITY
3) BASED ON LINKAGE BETWEEN GLYCON AND AGLYCON PORTION
4) BASED ON THERAPEUTIC NATURE OF GLYCOSIDE
Utilization of radioactive isotopes in the investigation of biogenetic studiesMs. Pooja Bhandare
Isotopes: TWO TYPES OF ISOTOPES,Radioactive isotopes.
Stable isotopes, Radiolabelled Tracers ( Radiolabelled compounds), Radiotracer Technique, Steps in Tracer Technique,
Selection of Radioisotopes.
Preparation of Radioisotopes.
Introduction/Insertion of Radiolabelled compound in biological system (Plant part) Seperation and determination of labelled compound in various biochemical reaction, Preparation of labelled compounds : Insertion of Radiolabelled compound in plant part, Root feeding, Stem feeding, Direct Injection, Floating Methods, Spray technique, Separation or Isolation of Radiolabelled compound and detection of radioisotope labelled compound. Detection and assay of Radioactive labelled compound, Detector system used (Analysis of Isotopic content). Method in Tracer Technique,
Precursor – Product sequence
Double and Multiple Labelling
. Competitive Feeding,Sequential Analysis
Applications of Tracer Technique
Medicinal chemistry 5 semester all synthesis Anjali Bhardwaj
Learn All
Medicinal Chemistry synthesis of
B.Pharmacy 5th Semester
As per PCI Syllabus
List Of Drug synthesis as per PCI Syllabus for B.Pharmacy 5th Semester
-Diphenhydramine hydrochloride -Furosemide
-Triprolidine hydrochloride -Methyldopate hydrochloride
-Promethazine hydrochloride -Disopyramide phosphate
-Cimetidine -Warfarin
-Meclorethamine -Tolbutamide
-Mercaptopurine -Benzocaine
-Methotrexate -Procaine
-Nitroglycerin -Dibucaine
-Isosorbide dinitrite
-Acetazolamide
-Chlorthiazide
Shikimic acid pathway is "metabolic pathway. "
,means metabolites are organic compounds synthesized by plant using enzyme mediated chemical reactions called metabolic pathway .
Now the metabolites are two types primary and secondary metabolites. The shikimic acid pathway is biosynthesis of secondary metabolites of phenylalanine, tyrosine and tryptophan(amino acid).
Glycosides play numerous important roles in living organisms. Many plants store chemicals in the form of inactive glycosides. These can be activated by enzyme hydrolysis, which causes the sugar part to be broken off, making the chemical available for use. Many such plant glycosides are used as medications. In animals and humans, poisons are often bound to sugar molecules as part of their elimination from the body.A glycoside is a molecule consisting of a sugar and a non-sugar group, called an aglycone. The sugar group is known as the glycone and can consist of a single sugar group or several sugar groups. The sugars is in its cyclic form and is covalently attached to the aglycon through the hydroxyl group of the hemiactal function.
There are many different kinds of aglycones. It can be a terpene, a flavonoid, a coumarin or practically any other natural occurring product (se figure 1)
The glycone can be attached to the aglycon in many different ways. The most common bridging atom is oxygen (O-glycoside), but it can also be sulphur (S-glycoside), nitrogen (N-glycoside) or carbon (C-glycoside). In general, one distinguishes between α-Glycosides and β-glycosides, depending on the configuration of the hemiactal hydroxyl group. The majority of the naturally occurring glycosides are β-glycosidesGenerally glycosides are more polar than the aglycones and as a result glycoside formation usually increases water solubility. This may allow the producing organism to transport and store the glycoside more efficiently
Many biologically active compounds are glycosides. The pharmacological effects are largely determined by the structure of the aglycone.
Glycosides comprise several important classes of compounds such as hormones, sweeteners, alkaloids, flavonoids and antibiotics
The shikimate pathway was discovered as the biosynthetic route to the aromatic amino acids phenylalanine, tyrosine, and tryptophan.
This pathway has been found only in microorganisms and plants. Phenylalanine and tryptophan are essential components of animal diets, and animals synthesize tyrosine in a single step from phenylalanine.
Biosynthesis of different types of amino acids.pptxlaija s. nair
Amino acids are the building blocks of proteins, playing a crucial role in various biological processes. They are categorized into essential and non-essential amino acids based on the body's ability to synthesize them. While essential amino acids must be obtained through the diet, non-essential amino acids can be synthesized by the body.
General Pathway of Amino Acid Biosynthesis:
Amino acid biosynthesis involves complex metabolic pathways that differ for each amino acid. However, a general overview can be provided:
Carbon Skeleton Formation:
Amino acids are composed of a central carbon atom (alpha carbon) bonded to a hydrogen atom, an amino group (NH2), a carboxyl group (COOH), and a side chain (R group) specific to each amino acid.
The carbon skeletons of amino acids are derived from intermediates of glycolysis, citric acid cycle, and pentose phosphate pathway.
Transamination:
A crucial step in amino acid biosynthesis is the transamination reaction, where an amino group is transferred from an amino acid donor to an alpha-keto acid acceptor.
This reaction is catalyzed by aminotransferases or transaminases, and pyridoxal phosphate (PLP) acts as a cofactor.
Specific Pathways for Essential Amino Acids:
Essential amino acids, which cannot be synthesized de novo by the body, have specific biosynthetic pathways.
For example, lysine and methionine biosynthesis involve the aspartate family pathway, while valine, leucine, and isoleucine biosynthesis occur through the branched-chain amino acid (BCAA) pathway.
Non-Essential Amino Acid Biosynthesis:
Non-essential amino acids can be synthesized by the body through various pathways.
For instance, glutamate serves as a precursor for the synthesis of several amino acids, including proline, arginine, and ornithine.
Specific Amino Acid Biosynthesis Pathways:
Serine and Glycine Biosynthesis:
Serine is derived from 3-phosphoglycerate and can be converted to glycine.
The enzyme serine hydroxymethyltransferase plays a key role in interconverting serine and glycine.
Histidine Biosynthesis:
Histidine biosynthesis involves a unique pathway that starts with phosphoribosyl pyrophosphate (PRPP) and includes several enzymatic steps.
Tyrosine and Phenylalanine Biosynthesis:
The shikimate pathway is essential for the biosynthesis of aromatic amino acids, including tyrosine and phenylalanine.
Chorismate is a key intermediate in this pathway.
Arginine Biosynthesis:
Arginine biosynthesis involves the urea cycle and the ornithine biosynthetic pathway.
Citrulline serves as a key intermediate in these processes.
Proline Biosynthesis:
Proline is derived from glutamate through a two-step reduction process involving pyrroline-5-carboxylate (P5C).
Regulation of Amino Acid Biosynthesis:
Amino acid biosynthesis is tightly regulated to maintain a balance between the body's requirements and energy conservation.
Feedback inhibition and genetic regulation play key roles in controlling the activity of enzymes involved in these p
Aromatic amino acids (AAA)- are amino acids that include an aromatic ring.
Examples include:
Among 20 standard amino acids:
phenylalanine (phe)
tryptophan (trp)
histidine (His)
tyrosine (tyr)
All plants and micro-organisms must synthesize their aromatic amino acids through the shikimate pathway in order to make proteins, unlike animals, which obtain them through their diet.
BIOSYNTHESIS OF PHOSPHOLIPIDS
Phospholipids:-
These are compounds containing, in addition to fatty acid and glycerol, phosphoric acid, nitrogenous bases, and another substituent. Polar compounds composed of alcohol attached by phosphodiester bridge to either diacylglycerol or sphingosine.
Amphipathic in nature has a hydrophilic head (phosphate +alcohol
eg., serine, ethanolamine, and choline) and a long, hydrophobic tail
(fatty acids or derivatives ).
- CLASSIFICATION OF PHOSPHOLIPIDS:-
- Glycerophospholipids
- Spingophospholipids or Sphingomyelin
- SYNTHESIS OF PHOSPHOLIPIDS
- FUNCTIONS OF PHOSPHOLIPIDS
- FUNCTIONS OF SPHINGOLIPIDS
introduction of Phenylalanine and Tyrosine , structures and metabolic fate of phenylalaine and tyrosine . different end product of Tyrosine ,: melanin and its types , epinephrine and norepinephrine, thyroide hormopne , different inheritance disease, PKU, Tyrosinemia type I, II & III, Albinism, Alkaptouria
catabolism of tyrosine
1. Measurement of Bioavailability:
Direct and indirect methods may be used to assess drug bioavailability. The in-vivo bioavailability of a drug product is demonstrated by the rate and extent of drug absorption, as determined by comparison of measured parameters, e.g., concentration of the active drug ingredient in the blood, cumulative urinary excretion rates, or pharmacological effects.
For drug products that are not intended to be absorbed into the bloodstream, bioavailability may be assessed by measurements intended to reflect the rate and extent to which the active ingredient or active moiety becomes available at the site of action.
The design of the bioavailability study depends on the objectives of the study, the ability to analyze the drug (and metabolites) in biological fluids, the pharmacodynamics of the drug substance, the route of drug administration, and the nature of the drug product.
Pharmacokinetic and/or pharmacodynamic parameters as well as clinical observations and in-vitro studies may be used to determine drug bioavailability from a drug product.
1.1. Pharmacokinetic methods:
These are very widely used and based upon the assumption that the pharmacokinetic profile reflects the therapeutic effectiveness of a drug. Thus these are indirect methods. The two major pharmacokinetic methods are:
The major pharmacokinetic methods are:
Plasma / blood level time profile.
o Time for peak plasma (blood) concentration (t max)
o Peak plasma drug concentration (Cmax)
o Area under the plasma drug concentration–time curve (AUC)
Urinary excretion studies.
o Cumulative amount of drug excreted in the urine (Du)
o Rate of drug excretion in the urine (dDu/dt)
o Time for maximum urinary excretion (t)
C. Other biological fluids
1.2. Pharmacodynamic methods:
IT involves direct measurement of drug effect on a (patho) physiological process as a function of time. Disadvantages of it may be high variability, difficult to measure, limited choices, less reliable, more subjective, drug response influenced by several physiological & environmental factors.
They involve determination of bioavailability from:
Acute pharmacological response.
Therapeutic response.
1.3. In-vitro dissolution studies
Closed compartment apparatus
Open compartment apparatus
Dialysis systems.
1.4. Clinical observations
Well-controlled clinical trials
Chemical preservatives for semisolids must be carefully evaluated for their stability with regard to the other components of the formulation as well as to the container. Plastic containers may absorb the preservative and thereby decrease the quantity available for inhibiting or destroying the microorganism’s responsible for spoilage. Some preservatives may sting or irritate the mucous tissues of the eye or nasal passages. Methylparabens and propylparabens tend to be more irritating when applied in the nose than quaternary ammonium compounds or the phenylmercuric salts. Boric acid may be used in the ophthalmic preparations, but is omitted from products to be used in the nose because of possible toxic effects if absorbed in large quantities.
These lecture slides, by Dr Sidra Arshad, offer a quick overview of physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar leads (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...VarunMahajani
Disruption of blood supply to lung alveoli due to blockage of one or more pulmonary blood vessels is called as Pulmonary thromboembolism. In this presentation we will discuss its causes, types and its management in depth.
The prostate is an exocrine gland of the male mammalian reproductive system
It is a walnut-sized gland that forms part of the male reproductive system and is located in front of the rectum and just below the urinary bladder
Function is to store and secrete a clear, slightly alkaline fluid that constitutes 10-30% of the volume of the seminal fluid that along with the spermatozoa, constitutes semen
A healthy human prostate measures (4cm-vertical, by 3cm-horizontal, 2cm ant-post ).
It surrounds the urethra just below the urinary bladder. It has anterior, median, posterior and two lateral lobes
It’s work is regulated by androgens which are responsible for male sex characteristics
Generalised disease of the prostate due to hormonal derangement which leads to non malignant enlargement of the gland (increase in the number of epithelial cells and stromal tissue)to cause compression of the urethra leading to symptoms (LUTS
Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
Factory Supply Best Quality Pmk Oil CAS 28578–16–7 PMK Powder in Stockrebeccabio
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Flu Vaccine Alert in Bangalore Karnatakaaddon Scans
As flu season approaches, health officials in Bangalore, Karnataka, are urging residents to get their flu vaccinations. The seasonal flu, while common, can lead to severe health complications, particularly for vulnerable populations such as young children, the elderly, and those with underlying health conditions.
Dr. Vidisha Kumari, a leading epidemiologist in Bangalore, emphasizes the importance of getting vaccinated. "The flu vaccine is our best defense against the influenza virus. It not only protects individuals but also helps prevent the spread of the virus in our communities," he says.
This year, the flu season is expected to coincide with a potential increase in other respiratory illnesses. The Karnataka Health Department has launched an awareness campaign highlighting the significance of flu vaccinations. They have set up multiple vaccination centers across Bangalore, making it convenient for residents to receive their shots.
To encourage widespread vaccination, the government is also collaborating with local schools, workplaces, and community centers to facilitate vaccination drives. Special attention is being given to ensuring that the vaccine is accessible to all, including marginalized communities who may have limited access to healthcare.
Residents are reminded that the flu vaccine is safe and effective. Common side effects are mild and may include soreness at the injection site, mild fever, or muscle aches. These side effects are generally short-lived and far less severe than the flu itself.
Healthcare providers are also stressing the importance of continuing COVID-19 precautions. Wearing masks, practicing good hand hygiene, and maintaining social distancing are still crucial, especially in crowded places.
Protect yourself and your loved ones by getting vaccinated. Together, we can help keep Bangalore healthy and safe this flu season. For more information on vaccination centers and schedules, residents can visit the Karnataka Health Department’s official website or follow their social media pages.
Stay informed, stay safe, and get your flu shot today!
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
Prix Galien International 2024 Forum ProgramLevi Shapiro
June 20, 2024, Prix Galien International and Jerusalem Ethics Forum in ROME. Detailed agenda including panels:
- ADVANCES IN CARDIOLOGY: A NEW PARADIGM IS COMING
- WOMEN’S HEALTH: FERTILITY PRESERVATION
- WHAT’S NEW IN THE TREATMENT OF INFECTIOUS,
ONCOLOGICAL AND INFLAMMATORY SKIN DISEASES?
- ARTIFICIAL INTELLIGENCE AND ETHICS
- GENE THERAPY
- BEYOND BORDERS: GLOBAL INITIATIVES FOR DEMOCRATIZING LIFE SCIENCE TECHNOLOGIES AND PROMOTING ACCESS TO HEALTHCARE
- ETHICAL CHALLENGES IN LIFE SCIENCES
- Prix Galien International Awards Ceremony
Anti ulcer drugs and their Advance pharmacology ||
Anti-ulcer drugs are medications used to prevent and treat ulcers in the stomach and upper part of the small intestine (duodenal ulcers). These ulcers are often caused by an imbalance between stomach acid and the mucosal lining, which protects the stomach lining.
||Scope: Overview of various classes of anti-ulcer drugs, their mechanisms of action, indications, side effects, and clinical considerations.
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
2. Commonly known as its anionic form shikimate, is a cyclohexene, a cyclitol and
a cyclohexanecarboxylic acid.
It is an important biochemical metabolite in plants and microorganisms.
Its name comes from the Japanese flower shikimi the Japanese star anise, Illicium
anisatum), from which it was first isolated in 1885 by Johan Fredrik Eykman.
The elucidation of its structure was made nearly 50 years later.
Shikimic acid is also the glycoside part of some hydrolysable tannins.
Shikimic acid
The shikimate pathway is a seven step metabolic route used by bacteria, fungi,
algae, parasites, and plants for the biosynthesis of aromatic amino acids
(phenylalanine, tyrosine, and tryptophan).
This pathway is not found in animals; therefore, phenylalanine and tryptophan
represent essential amino acids that must be obtained from the animal's diet
Animals can synthesize tyrosine from phenylalanine, and
therefore is not an essential amino acid except for individuals
unable to hydroxylate phenylalanine to tyrosine).
3.
4. Phosphoenolpyruvate and erythrose-4-phosphate react to form 2-keto3-
deoxy7phosphoglucoheptonic acid, in a reaction catalyzed by the enzyme DAHP
synthase.
2-keto3-deoxy7phosphoglucoheptonic acid is then transformed to 3-dehydroquinate
(DHQ), in a reaction catalyzed by DHQ synthase.
Although this reaction requires nicotinamide adenine dinucleotide (NAD) as a cofactor,
the enzymic mechanism regenerates it, resulting in the net use of no NAD.
5. DHQ is dehydrated to 3-dehydroshikimic acid by the enzyme 3-dehydroquinate
dehydratase, which is reduced to shikimic acid by the enzyme shikimate
dehydrogenase, which uses nicotinamide adenine dinucleotide phosphate
(NADPH) as a cofactor.
The next enzyme involved is shikimate kinase, an enzyme that catalyzes the ATP-
dependent phosphorylation of shikimate to form shikimate 3-phosphate. Shikimate
3-phosphate is then coupled with phosphoenol pyruvate to give 5-
enolpyruvylshikimate-3-phosphate via the enzyme 5-enolpyruvylshikimate-3-
phosphate (EPSP) synthase.
Then 5-enolpyruvylshikimate-3-phosphate is transformed into chorismate by a
chorismate synthase.
6. Prephenic acid is then synthesized by a Claisen rearrangement of chorismate by
Chorismate mutase.
Prephenate is oxidatively
decarboxylated with retention
of the hydroxyl group by
Prephenate dehydrogenase
to give p-
hydroxyphenylpyruvate,
which is transaminated using
glutamate as the nitrogen
source to give tyrosine and
α-ketoglutarate.
7. Role of Shikimic Acid Pathway:
• Starting Point in The Biosynthesis of Some Phenolics
Phenyl alanine and tyrosine are the precursors used in the biosynthesis of
phenylpropanoids. The phenylpropanoids are then used to produce the
flavonoids, coumarins, tannins and lignin.
• Gallic acid biosynthesis
Gallic acid is formed from 3-dehydroshikimate by the action of the enzyme
shikimate dehydrogenase to produce 3,5-didehydroshikimate. The latter
compound spontaneously rearranges to gallic acid.
• Other compounds
•Shikimic acid is a precursor for:
indole, indole derivatives and aromatic amino acid tryptophan and tryptophan
derivatives such as the psychedelic compound dimethyltryptamine.
many alkaloids and other aromatic metabolites.
8.
9. • In the pharmaceutical industry, shikimic acid from the Chinese star anise (Illicium
verum) is used as a base material for production of oseltamivir (Tamiflu).
Uses:
Shikimate can be used to synthesize (6S)-6-Fluoroshikimic acid, an
antibiotic which inhibits the aromatic biosynthetic pathway.
Glyphosate, the active ingredient in the herbicide Roundup, kills plants by
interfering with the shikimate pathway in plants. More specifically,
glyphosate inhibits the enzyme 5-enolpyruvylshikimate-3-phosphate
synthase (EPSPS). "Roundup Ready" genetically modified crops overcome
that inhibition.
Target for drugs
10. • “Plant Secondary Metabolism” By David S. Seigler
• “Shikimic acid: metabolism and metabolites” by
Edwin Haslam
• “Shikimic Acid Pathway” by N. P. Botting Pergamon
Press, 1993 - 66 pages
• http://www.ncbi.nlm.nih.gov/pubmed/15012217
• http://www.naturalproduct.skku.edu/erp/erpmenu
s/lesson_pds/.../shikimate.pdf
• http://www.life.illinois.edu/ib/425/lecture8.html