What Is Bt Cotton?

What Is Bt(Bacillus thuringiensis) Cotton?

Bt Cotton is a genetically modified cotton crop that has one or two genes of a soil bacterium inserted into the seeds of cotton.

History

 Bt Cotton seeds were introduced by Bollgard Cotton, a trademark of the Monsanto group. Bt Cotton was first introduced to the U.S. in 1996 according to the University of California San Diego and was aimed at reducing the effects of the tobacco budworm and the pink bollworm. Tests began at the same time around the world on crossing the American Bt Cotton seeds with cotton produced in other countries, including India, according to the Science & Development Network. Later versions of Bt Cotton were introduced in 2003 and 2004 aimed at reducing the impact of a wider range of insects than the original version.

Bacterium

 The University of California San Diego describes Bt Cotton as containing a bacterium called Bacillus Thuringiensis (Bt). The spores of Bt produce crystal proteins which are toxic to many forms of insects, leading to its use as an insecticide. The University of California San Diego reports Bt is found throughout the world in a variety of soils in very small amounts producing thousands of different strains of Bt. The University of California San Diego reports Bt does not produce food poisoning proteins, Despite being a member of the food poisoning Bacillus Cerus family of bacterium; Bt Cotton has a very small chance of cross contamination due to its lack of use in food production.

Benefits

 The benefits provided by Bt Cotton are explained by the University of California San Diego as including a reduced cost per acre of between $25 and $65 in the years of 1996 to 1998 from the spraying of insecticides. Bt Cotton crops are estimated by the University of California San Diego to have yielded around 5% more cotton than traditionally grown cotton crops planted during the same time period.

Problems

According to the Science and Development Network, Bt Cotton crops in India are being affected by the bollworm that is becoming resistant to the Bt toxins and proteins produced by Bt Cotton. Bt Cotton is one of the 21 genetically modified crops introduced to 21 countries around the world by 2006. Four of the 21 crops are reported by the Science and Development Network to have been affected by insects resistant to the insecticides initially introduced to the crops.

Insecticide

The insecticide introduced to each version of Bt Cotton is reported by the University of California San Diego to be created to be specific to the insect at which it is aimed. The use of Bt Cotton as an organic form of insecticide is commonly used in organic farming and in aerial spraying of urban areas.
Sources:http://www.ehow.com/about_6372845_bt-cotton_.html

What Is the Bt(Bacillus thuringiensis) Gene?

 What Is the Bt(Bacillus thuringiensis) Gene?

Bacillus thuringiensis, or Bt, is a type of bacterium found in soil. Bt bacteria produce protein crystals known to be toxic to several varieties of insect larvae, including moths, beetles, mosquitoes, black flies, nematodes and flatworms. The Bt gene is a small stretch of DNA from the Bt chromosome that codes for the production of these protein crystals. Davidson College states that both Bt bacteria and the Bt gene products are used as insecticides in the U.S., Canada, Argentina, South Africa and parts of Europe.

History:

 Bt bacteria were discovered in 1901 in Japan, and were brought to the U.S. in 1958 for agricultural use. Initially, the bacteria were grown and harvested to be used as crop sprays and dusts, according to Davidson College. As the field of genetic engineering evolved and the Bt gene was identified and isolated, it became one of the first genes to be inserted directly into the hereditary structure or genome of plant crops, creating genetically modified Bt crops. In doing so, the plants themselves were able to produce the toxic protein crystals and thus become resistant to Bt affected insects without the need for spraying.

Uses:

Today the Bt gene has been incorporated into a variety of cash crops grown and sold around the globe, including corn, potatoes, broccoli, cauliflower, cotton and tobacco. Whole Bt bacteria are still dusted in U.S. forests to control spruce budworms and gypsy moths, according to Iowa State University. Bt is also used in common household insecticide sprays intended for garden use.

Benefits:

Bt is washed away from plants with water or rain, and it is broken down by sunlight. These properties convey an environmental benefit. However, as the Bt must be eaten by insects to be effective, this trait makes Bt a less potent insecticide than some synthetics which kill on contact. By genetically engineering crops to contain the Bt gene and be constantly producing their own Bt toxin, the plant will be insect resistant regardless of weather patterns. Bt crops can also kill insects even after they have invaded the plant tissues, as reported by Iowa State University.

Safety

Both Bt crops and commercially produced Bt insecticides are classified as "Generally Regarded as Safe" (GRAS) by the Environmental Protection Agency. The protein crystal which is toxic to insects is safe for human consumption, as humans lack the digestive enzyme required to convert the protein to its toxic form, according to Davidson College. Studies of Bt's effects on animals have produced contradictory results, and it is lethal to Monarch butterflies.

Considerations

One cost of producing Bt crops is that insect resistance will still occur, likely at a higher rate than it would in non-Bt crops. Bt will kill most of a given species of insect, but never all of them. Of those that survive, a high percentage of them will be naturally Bt resistant, becoming the parents of future generations. A second issue with genetically modified crops involves gene flow, the unintentional transfer of genes from one plant species to another, according to Davidson College. This may occur through pollination of Bt crops grown in close geographic proximity to other crops, thereby introducing Bt genes into other plants.
  
Source:http://www.ehow.com/about_7238414_bt-gene_.html

Procedure For DNA Fingerprinting

Procedure for DNA fingerprinting involves following steps:

    1. Performing a Southern Blot
     2. Making a Radioactive Probe
     3. Creating a Hybridization Reaction
     4. VNTRs 

• Southern Blot

  The Southern Blot is one way to analyze the genetic patterns which appear in a person's DNA. Performing a Southern Blot involves:
  
  1. Isolating the DNA in question from the rest of the cellular material in the nucleus. This can be done either chemically, by using a detergent to wash the extra material from the DNA,or mechanically, by applying a large amount of pressure in order to "squeeze out" the DNA.
  
  2. Cutting the DNA into several pieces of different sizes. This is done using one or more restriction enzymes.
  
  3. Sorting the DNA pieces by size. The process by which the size separation, "size fractionation," is done is called gel electrophoresis. The DNA is poured into a gel, such as agarose, and an electrical charge is applied to the gel, with the positive charge at the bottom and the negative charge at the top. Because DNA has a slightly negative charge, the pieces of DNA will be attracted towards the bottom of the gel; the smaller pieces, however, will be able to move more quickly and thus further towards the bottom than the larger pieces. The different-sized pieces of DNA will therefore be separated by size, with the smaller pieces towards the bottom and the larger pieces towards the top.
  
  4. Denaturing the DNA, so that all of the DNA is rendered single-stranded. This can be done either by heating or chemically treating the DNA in the gel.
  
  5. Blotting the DNA. The gel with the size-fractionated DNA is applied to a sheet of nitrocellulose paper, and then baked to permanently attach the DNA to the sheet. The Southern Blot is now ready to be analyzed.
  
  
  In order to analyze a Southern Blot, a radioactive genetic probe is used in a hybridization reaction with the DNA in question (see next topics for more information). If an X-ray is taken of the Southern Blot after a radioactive probe has been allowed to bond with the denatured DNA on the paper, only the areas where the radioactive probe binds [red] will show up on the film. This allows researchers to identify, in a particular person's DNA, the occurrence and frequency of the particular genetic pattern contained in the probe. 
  
  

   Making a Radioactive Probe  

  1.Obtain some DNA polymerase [pink]. Put the DNA to be made radioactive (radiolabeled) into a tube.
        
  2.Introduce nicks, or horizontal breaks along a strand, into the DNA you want to radiolabel. At the same time, add individual nucleotides to the nicked DNA, one of which,*C [light blue], is radioactive. 
   
  3.Add the DNA polymerase [pink] to the tube with the nicked DNA and the individual nucleotides. The DNA polymerase will become immediately attracted to the nicks in the DNA and attempt to repair the DNA, starting from the 5' end and moving toward the 3' end. 
   
  4.The DNA polymerase [pink] begins repairing the nicked DNA. It destroys all the existing bonds in front of it and places the new nucleotides, gathered from the individual nucleotides mixed in the tube, behind it. Whenever a G base is read in the lower strand, a radioactive *C [light blue] base is placed in the new strand. In this fashion, the nicked strand, as it is repaired by the DNA polymerase, is made radioactive by the inclusion of radioactive *C bases.  
     
  5.The nicked DNA is then heated, splitting the two strands of DNA apart. This creates single-stranded radioactive and non-radioactive pieces. The radioactive DNA, now called a probe [light blue], is ready for use.
  
  
  

  • Creating a Hybridization Reaction

     
    Creating a Hybridization Reaction
    
    1. Hybridization is the coming together, or binding, of two genetic sequences. The binding occurs because of the hydrogen bonds [pink] between base pairs. Between a A base and a T base, there are two hydrogen bonds; between a C base and a G base, there are three hydrogen bonds.
    
    
    2. When making use of hybridization in the laboratory, DNA must first be denatured, usually by using heat or chemicals. Denaturing is a process by which the hydrogen bonds of the original double-stranded DNA are broken, leaving a single strand of DNA whose bases are available for hydrogen bonding.
    
    
    3. Once the DNA has been denatured, a single-stranded radioactive probe [light blue] can be used to see if the denatured DNA contains a sequence similar to that on the probe. The denatured DNA is put into a plastic bag along with the probe and some saline liquid; the bag is then shaken to allow sloshing. If the probe finds a fit, it will bind to the DNA.
     
    4. The fit of the probe to the DNA does not have to be exact. Sequences of varying homology can stick to the DNA even if the fit is poor; the poorer the fit, the fewer the hydrogen bonds between the probe [light blue] and the denatured DNA. The ability of low-homology probes to still bind to DNA can be manipulated through varying the temperature of the hybridization reaction environment, or by varying the amount of salt in the sloshing mixture.
    
    
    

    • VNTRs(Variable Number Tandem Repeats)

      
      
      • Every strand of DNA has pieces that contain genetic information which informs an organism's development (exons) and pieces that, apparently, supply no relevant genetic information at all (introns). Although the introns may seem useless, it has been found that they contain repeated sequences of base pairs. These sequences, called Variable Number Tandem Repeats (VNTRs), can contain anywhere from twenty to one hundred base pairs.
      
      
      • Every human being has some VNTRs. To determine if a person has a particular VNTR, a Southern Blot is performed, and then the Southern Blot is probed, through a hybridization reaction, with a radioactive version of the VNTR in question. The pattern which results from this process is what is often referred to as a DNA fingerprint.
      • A given person's VNTRs come from the genetic information donated by his or her parents; he or she could have VNTRs inherited from his or her mother or father, or a combination, but never a VNTR either of his or her parents do not have. Shown below are the VNTR patterns for Mrs. Nguyen [blue], Mr. Nguyen [yellow], and their four children: D1 (the Nguyens' biological daughter), D2 (Mr. Nguyen's step-daughter, child of Mrs. Nguyen and her former husband [red]), S1 (the Nguyens' biological son), and S2 (the Nguyens' adopted son, not biologically related [his parents are light and dark green]).
      
      
      • Because VNTR patterns are inherited genetically, a given person's VNTR pattern is more or less unique. The more VNTR probes used to analyze a person's VNTR pattern, the more distinctive and individualized that pattern, or DNA fingerprint, will be. 
      Source:http://protist.biology.washington.edu/fingerprint/dnaintro.html

DNA Fingerprinting

 DNA Fingerprinting

• The chemical structure of every one'sDNA is same. The only difference between people (or any animal) is the order of the base pairs. There are so many millions of base pairs in each person's DNA that varies from one to other.

• Using these sequences, every person could be identified solely by the sequence of their base pairs. However, because there are so many millions of base pairs, the task would be very time-consuming. Instead, scientists are able to use a shorter method, because of repeating patterns in DNA.

• These patterns do not, however, give an individual "fingerprint," but they are able to determine whether two DNA samples are from the same person, related people, or non-related people. Scientists use a small number of sequences of DNA that are known to vary among individuals a great deal, and analyze those to get a certain probability of a match.

Polytene Chromosomes

Polytene chromosomes

Polytene chromosomes are specific interphase chromosomes consisting of thousands of deoxyribonucleic acid (DNA) strands. For this reason they are very large and display a characteristic band–interband morphology. Polyteny arises in tissues, organs and at developmental stages when there is need for the rapid development of an organ at an unaltered high level of function. Organs containing cells with polytene chromosomes are, as a rule, involved in intense secretory functions accomplished during a short time against a background of rapid growth. Chromosome rearrangements and in situ hybridization on polytene chromosomes allow genes to be mapped to a resolution of a few tens of kilobases. Polytene chromosomes allow a specific narrow region to be dissected out with a micromanipulator and a library of DNA clones to be derived from the region.

Important facts

Polytene chromosomes are specific type of interphase chromosomes consisting of thousands of DNA strands.
Polytene chromosomes have been found in many tissues of the representatives of two orders of insects: Diptera and Collembola, in the macronuclear anlagen of Infusoria, in certain organs and tissues of mammals and also in the cells of the synergids, antipods and endosperm of angiospermous plants.
Polyteny arises in tissues, organs and at developmental stages when there is need for the rapid development of an organ at an unaltered high level of function. Organs containing cells with polytene chromosomes are, as a rule, involved in intense secretory functions accomplished during a short time against a background of rapid growth.
Along the linear axis polytene chromosome have variation in the concentration of the chromatin. Regions of high concentrations are known as chromomeres (bands), and regions with low concentrations are known as interchromomeres (interbands).
The pattern of bands and interbands in each polytene chromosome is specific for the species, and in general is characteristic of that particular chromosome in different tissues or at different developmental stages.
Polytene chromosomes are now considered to be very important objects for the analysis of numerous features of interphase chromosome organization and the genome as a whole.
Keywords: genes; puffs; bands; interbands; heterochromatin

Golden Rice:Transgenic Crop

Golden Rice:Transgenic Crop

Introduction

At a New Delhi Biotechnology workshop on February 12, 2001, Professor Ingo Potrykus, Swiss Federal Institute of Technology, Zurich, announced that India will receive technology transfer for the production of Golden Rice, free of encumbrances and license fee.This news brought much cheer into the hearts of many in the country, but most people are blissfully unaware of the stormy seas of controversies in which a handful of nascent seeds of Golden Rice are struggling to survive and to become global giving succor to many a poor.
Golden Rice is an important issue for countries like India.Public awareness of the benefits of this product will help in preventing  repeats of what has been happening with B.T cotton in India.

What is Golden Rice?
Golden Rice is a transgenic variety of rice, with genes for the synthesis of beta-carotene taken from the temperate garden favorite Narcissus pseudo narcissus (daffodil) and inserted into the genome of a temperate strain of rice, using Agrobacterium tumefaciens as the vector, to effect the transfer.The gene construct also contains some genes for enzymes of the bio synthetic pathway of b-carotene, from another bacterium  Erwinia uredovora.The grains of this Genetically Modified (GM) rice  are similar to other varieties, in their crinkly and scabrous husks but the core of the grain is pale yellow, instead of pearly white.The color is due to b-carotene, which makes this the Golden Rice, more so because b-carotene is very important to our health.

The detailed technology used to develop Golden Rice was published by Potrykus and his associates, in Science (vol. 287,  pp 303-305, January, 2000). Ever since Professors Ingo Potrykus  and Peter Beyer (University of Freiburg, Germany) have announced their success in producing Golden Rice, about a year ago, there has been an incessant increasingly polarized public debate over the pros and cons of not just Golden Rice, but all GM crops and organic produce. 
 

The Carotenoid Pool

• About 600 structures of a group of chemical compounds called carotenoids have been discovered in various organisms, but predominantly confined to plants.
• The carotene are hydrocarbons, while the other carotenoids  also contain oxygen.The carotenoids are insoluble in water but are soluble in fats and organic solvents.
•  Several carotenoids occur simultaneously in organisms, and are in a continuous state of metabolic flux. They are referred together as the carotenoid pool, the same way as the amino acid pool  and the nucleotide pool.   
• About 150 of the carotenoids are widely found, among which about 20 closely related carotenoids occur in a wide variety of higher plants,  sea weeds,  animals, fungi and bacteria.    
• Carotenoids are light harvesting pigments located in the plastids.   
• The carotenoids in the chloroplasts protect chlorophyll from damage by excessive light. The carotenoids, related to and derived from b-carotene, impart pale yellow to light reddish yellow colour to the parts in which they occur.   
• Organisms contain different combinations and quantities of carotenoids in different parts.   
• Leaves and other green parts, anthers, pollen, styles and stigmas, fruits and seeds of several species of plants contain carotenoids.   
• Leafy vegetables, mangoes, peaches,  oranges, saffron, maize kernels, yellow-red  coloured pulses, carrots, beetroot, sweet potato, etc., are the common examples.   
• In the earlier days, the techniques of chemical analysis were not sophisticated enough to precisely distinguish one carotenoid from the other, and quantify them.   
• Hence most of the earlier literature collectively called them all carotenoids.   
• HPLC is now routinely used to isolate and quantify different carotenoid compounds.    

  The more important of the carotenoids and their sources are listed below:

1. a-carotene:  leaves and roots of carrots, and the fruit of red palm oil plant 
2. b-carotene:  a very large number of plants and animals, abundant in brown sea
3.                        weeds but exceptionally high concentrations in the daffodils
4. d-carotene:   tomato fruits  
5. g-carotene:   many flowers and fruits, but more abundant in the fungi 
6. Lycopene:    tomato fruit
7. b-cryptoxanthin: maize seeds, eggs, butter, and blood.  
8. Spirilloxanthine: photosynthetic bacteria and some fungi 
9. Lutein (xanthophylls): flowers, fruits, seeds, eggs and animal fats 

As humans and animals cannot synthesize carotenoids, they must be obtained from vegetable dietary sources. 

 
b-Carotene, Vitamin-a and our health

1.   b-carotene is extremely important to us as it is the  most efficient precursor of retinol  (vitamin-A), hence it is called pro-vitamin-A.    
2. The liver converts b-carotene into vitamin-A, the only way we can get our requirement of vitamin-A.  
3. Specific enzymes split one molecule of b-carotene into two molecules of vitamin-A.
4.  Deficiency of vitamin-A causes dry skin, dry eyes, dry mucous surfaces, retarded development and growth, sterility in males and night blindness and other types of irreversible blindness.
5.  Every year, at least a million children die weakened by vitamin-A deficiency and about 3,50,000 others go blind.   Millions of others, young and old, suffer from several disorders related to vitamin-A deficiency (VADs).   

Lycopene 

Lycopene and lutein do not yield vitamin-A.   

a-carotene and b-cryptoxanthin are converted into vitamin-A, but only one molecule of vitamin-A is formed from one molecule of these compounds, while the rest of the molecule adds to the chemical debris of the body.Hence, maize kernels, eggs and animal fats like butter are poor sources of pro-vitamin-A, while tomato is not a source at all.  

 
Disease Prevention By b-Carotene

• In recent times, b-carotene has been rated high as an antioxidant which scavenges free-radicals, which are believed to be involved in the onset of several disorders, including cardio-vascular disease and certain types of cancer
•  b-carotene is being increasingly used as a preventive measure against these diseases.

 
Our Sources Of b-Carotene

• The rice plant produces b-carotene in the green tissues but there is none in the starchy endosperm which constitutes  90 percent of the grain we eat.  
• Most of us get the required amount of b-carotene from supplementary food such as carrots, fruits and leafy vegetables.   
• Several communities, such as the Japanese, consume brown sea weeds, which are high in b-carotene.    
• Throughout the world, the poor do not get enough of b-carotene and hence suffer from vitamin-A deficiency.   
• Vitamin-A deficiency may also be due to certain diseases like measles.  

Why Golden Rice?
About a dozen years ago, Gary Toenniessen, Director of Food Security, Rockefeller Foundation, has recognized the lack of b-carotene in polished rice and identified as a worthwhile goal,  the transfer of genes for b-carotene synthesis into food grains, particularly rice,  using transgenic technology.Such a fine tuned task is beyond the possibilities of traditional plant breeding techniques to achieve. 

• Potrykus saw a hope for millions of poor children in introducing the gene for b-carotene in the rice itself, which is the staple food.   
• The synthesis of b-carotene in plants is a complex process controlled by several genes, which make the task of producing a transgenic much more difficult.  
• Peter Beyer, an expert on the biosynthetic pathway of b-carotene in daffodils, became an associate.   
• The choice of daffodils as the source of b-carotene genes is a very clever one, as they have an exceptionally high concentration of b-carotene, all of which can be converted into vitamin-A, but unfortunately no part of daffodils is edible.

Synthesis of Golden Rice

Potrykus and Beyer faced several difficulties in creating Golden Rice, the more important being:  
a) The transfer of a set of several genes together proved to be a formidable task;  
b)  Rice plants did  not grow well in green houses; and  
c) The genes they transferred and the bacteria used for such transfer were encumbered 
    by patents and proprietary rights. 
 
Finally all the difficulties were overcome.The success was achieved, more importantly,  without industrial financial support.The owners of different patents, Syngenta, Monsanto and four other companies, recently agreed to donate the technology free to developing countries, in exchange for commercial marketing rights in the US and other affluent markets.   The concession offered by the patent owners is the basis for the announcement by Potrykus, at New Delhi,  on a free transfer of technology to India.An appreciable gesture,  but sneered at by the Rural Advancement Foundation International, as “a rip-off of the public trust”.  

Challenges Ahead
A decade’s dream of Potrykus has been realised, but a lot more is yet to be done, the following being the more important challenges:
  a) the gene set has to be transferred to a tropical variety of rice since the temperate
    variety will not fare well  nor will it be accepted, in the tropics;
  b) years’ of lab and field work on perfecting a viable Golden Rice varieties suitable
    for  different agro-climatic zones of India, need to be developed; 
  c) currently the quantity of b-carotene in the golden rice is not good enough to
    provide a substantial quantity of it, at the normal 300g of rice eaten per
    day; 
  d) the product should be affordable to the very poor of the world, for which it should
    get into the Public Distribution System,  and 
  e) the hostile, sometimes violent,   protestors have to be satisfied on the safety (some
   gene products may cause allergies, some GM crops are feared to become    gregarious weeds) and utility of the product (the ultimate desired  benefit may not be available in the end).  

Do GM Crops Become Threatening Weeds?

Amidst the disturbing controversy, an article in the journal Nature (February 8, 2001) came as a whiff of fresh air.   A ten year study in UK by Michael Crawley and team  has shown that GM crops hardier than rice, such as maize, beet, oilseed rape and   potato, did not become more competitive than their non-GM counterparts and did not invade the environment .Rice is a very delicate plant. Golden Rice becoming gregarious is far beyond the realm of possibilities.

Fool’s Gold?
The Greenpeace organization, which is at the forefront of criticism of biotechnology products, posted a statement on the internet on February 9, 2001, and dubbed Golden Rice as ‘Fool’s Gold’.   The criticism is based on the following points:
  a) The promoters of Golden Rice and supporters of GM crops have gone too far in over selling the product as for example by such statements as Syngenta’s projection that a single month’s marketing delay of Golden Rice will cause 50,000 children to go blind;
  b) An adult would have to eat 3.7kg of raw  (around 9kg of cooked) Golden Rice, as
      against the normal intake of 300g of raw rice a day,  to get the daily requirement 
      of b-carotene;  and    
  c)The underlying causes of vitamin-A deficiency (poverty and lack of access to more
      diverse diet) were not addressed and short term measures such as supplementation    
      (e.g., pills) and food fortification which are cheap and effective were not considered.
 

• At a Press Conference on February 9, 2001, at Lyon, France, Ingo Potrykus conceded that the quantity of b-carotene available in the current sample of Golden Rice is small and needs to be improved.   
• He pointed out that it was never meant that Golden Rice alone would supply the entire daily requirement.   
• He assured that golden rice does not compete with alternative and traditional interventions but rather complements them.  

•   With the possibility of wheat, cassava, sweet potato, banana, etc.,  going gold in the future, alternatives to Golden Rice will be several.   
• The future crops will also address other deficiencies such as iron, essential amino acids, etc. 
• Some Points To Ponder Amidst these emotionally charged, and seemingly uncompromising positions of the protagonists  and antagonists of GM crops, we should keep in mind certain issues, particularly in the context of Golden Rice.  
• The concept of balance diet has come into practice as people have realised a very long time ago that no single (or even a few) food items can provide all the nutrients we need.     Potrykus says that Goldeb Rice can now provide 20-40 per cent of the daily requirement.   
• Those who eat Golden Rice would get at least some b-carotene, which certainly will compensate marginal deficiencies.  
• There is no dearth for sources of b-carotene in most countries.     
• There are about 160 species of plants in India, used as food and/or medicine, which contain very considerable amounts of b-carotene in their carotenoid pool.    
• Greenpeace suggested supplementation through pills.   
• As purified b-carotene is expensive costing  about US $ 185/25mg, administration of the recommended dose (5mg/day) through pills  is not feasible.  
• Greenpeace suggested red palm oil as a source of pro-vitamin-A, but what this contains abundantly is a-carotene, which is only half as efficient as b-carotene in terms of conversion into vitamin-A.  
• Besides, palm oil contains about 48 per cent of palmitic acid, a saturated fatty acid, which is not so good for our health.   Then, how much of palm oil one can consume?   How much of it actually is available to the poor who cannot afford even the more commonly available leafy vegetables?
• Vitamin-A requires a (mostly endogenous) protein and palmitic acid to be stable and functional in our body.  
• It also requires tocopherol (vitamin-E), an antioxidant that makes it more stable.   
• When these substances are not present in the existing varieties of rice and other cereals, it is very unreasonable to expect Golden Rice to contain them.  
• May be if given a chance, the future varieties of Golden Rice may contain these stabilising compounds.   
• Their absence does not make Golden Rice a useless product.
• Golden Rice is now only a research product and it takes a lot of time and effort to make it available across the counter, particularly in the developing countries,  which essentially require it.   
• Controversial issues can be settled only through relevant experimental data and discussion

Benefits of Golden Rice  

• Benefits of Golden Rice at the poorest of the poor who cannot get anything other than rice, green chillies and salt, if at all.   
• Traditional wisdom taught all communities to eat adequate quantities of pulses, green vegetables and fruits.   
• But affordability, not availability,  is the problem.   
• Even when Golden Rice is on the market, affordability will be the spoiler, though free technology transfer is a blessing.  
• Even those who can afford supplementary foods do not often get adequate quantities of b-carotene, for various individual metabolic deficiencies or merely out of ignorance.  
• Just as the compulsory use iodised salt, even by those who do not need it, has been introduced so that those needing iodine would get it, Golden Rice too will provide for a compulsory intake of some quantity of b-carotene.  
•  This is to save millions of children in the developing world, from blindness and death

High Security for Biotechnology?
In a civilised society hooliganism and vandalism have no place.   
Destroying or burning GM trial plots, vandalising research laboratories are abominable criminal acts, which transgress the intellectual and material property rights of others.     
Discussion and not destruction is the need of the hour. 
The degree of scare implanted by  biotech antagonists on the minds of biotechnology researchers, is reflected by the fact that Golden Rice seeds are protected in a grenade proof bunker in Switzerland!

Golden Rice Deserves A Chance

• Golden rice and other GM crops are meant to revolutionize agriculture.
• Golden Rice signifies a shift in the target of GM crops, from the farmer to the consumer.     
•  It has the potential to help millions throughout the developing world.   
• Millions of poor in the developing world need it.    
• Golden Rice deserves to be given a chance to prove itself or to the contrary.   Let us hope that the dust settles soon and the sun shines on Golden Rice.

Agrobacterium Mediated Gene Transfer- Genetic Engineering

 Agrobacterium Mediated Gene Transfer- Genetic Engineering

Agrobacterium mediated gene transfer is one of the most widely used methods of gene transfer. Agrobacterium tumefaciens is a bacterial plant pathogen found in the soil which causes crown gall disease in plants.The basic mechanism that works behind it is, transfer of a segment or small piece of bacterial DNA to the plant genome. This bacterial DNA segment gets incorporated in the plant genome, stabilizes there and transcribes or expresses itself.The bacterial DNA causing disease is situated on a plasmid, Ti plasmid (Tumour inducing plasmid, 200kb) instead of on a bacterial chromosome.
The segment which is actually transferred to plant genome is situated on T-DNA (transferred DNA, 23kb) of this plasmid. 
In the expression of disease symptom, two major sets of genes are involved

•     Genes on T-DNA (total 15 genes)
•     Virulence genes i.e. vir genes

Both of the above sets of gene can be present on the same plasmid (co-integrative vectors) or separate plasmid (binary vector).
1.Genes on T-DNA
The T-DNA contains two types of genes, which possess the ability to express in plants:

1.  Oncogenes – Encode for synthesis of auxins and cytokinins (phytohormones). The overproduction of phyto-hormones leads to proliferation of callus or tumour formation. 
2. Opine synthesizing genes – Encode for synthesis of opines (a product from amino acids + sugars, which are produced and excreted by the crown gall infected cells and consumed by A. tumefaciens as carbon and nitrogen sources this means opines act as source of nutrient for bacteria

 
 2.Virulence Genes 
These are located on vir region (30 kb) of Ti plasmid.These genes are not transferred to the plant genome, just help in the process; organized in six operons that are essential for the transfer (virA, virB, virD, and virG) or increase transfer efficiency (virC and virE) of T-DNA.They are involved in activities like recognition of host plant, the chemotaxis, attachment to the plant cell, transfer of DNA in plant cell nucleus and integration of inserted DNA into the plant chromosome.
Procedure :
 For transformation oncogenic T-DNA is removed and replaced by another desired DNA segment with border sequence.While working binary vectors the vir genes are removed and the desired DNA is integrated between the borders.The vir genes necessary for transfer to the plant genome are arranged on a second plasmid with T-DNA and both borders removed.Such binary vectors restrict the transferred Ti plasmid from spreading uncontrollably as genes responsible for that are do not get transferred.
Advantages of Agrobacterium mediated gene transfer 

•     Simple and comparatively less expensive
•     High transformation efficiency
•     Transgenic crop obtained have better fertility percentage
•     Today, protocols for both monocotyledons and dicotyledons are available
•     Relatively large length chromosomal segment can be transferred with little arrangement

Disadvantages of Agrobacterium mediated gene transfer 

•     Time consuming
•     Not all kind of cells can be treated by this method
•     Can not transform organelles
•     Sometimes leads to false positive results

    Genetic engineering Techniques
    Gene Transfer
    Agrobacterium – Gene Transfer