Type of Corn
Type of Corn
Corn, Zea mays, is an annual grass in the family Poaceae and is a staple food crop grown all over the
world. The corn plant possesses a simple stem of nodes and internodes. A pair of large leaves extends
off of each internode and the leaves total 8–21 per plant. The leaves are linear or lanceolate (lance-
like) with an obvious midrib and can grow from 30 to 100 cm (11.8–39.4 in) in length. The male and
female inflorescences (flower bearing region of the plant) are positioned separately on the plant. The
male inflorescence is known as the 'tassel' while the female inflorescence is the 'ear'. The ear of the
corn is a modified spike and there may be 1–3 per plant. The corn grains, or 'kernels', are encased in
husks and total 30–1000 per ear. The kernels can be white, yellow, red, purple or black in color. Corn
is an annual plant, surviving for only one growing season prior to harvest and can reach 2–3 m (7–10
ft) in height. Corn may also be referred to as maize or Indian corn and is believed to originate from
Mexico and Central America.
https://plantvillage.psu.edu/topics/corn-maize/infos
“Corn (Maize).” Cress | Diseases and Pests, Description, Uses, Propagation, PlantVillage , 2017,
plantvillage.psu.edu/topics/corn-maize/infos.
Symptoms of Infestation
Damage to corn caused by the common stalk borer is characterized by wilting and/or dying of the
upper leaves or by ragged irregular holes chewed in the newly unrolled leaves. The characteristic
"dead heart" is caused by the insect boring into the stalk at the soil level and tunneling upward. It may
also climb up the plant and tunnel downward into the whorl, creating the ragged holes. A considerable
amount of "frass", or sawdust-like borer feces, can be seen in the whorl or coming out of the borer's
entry hole in the stalk. Corn plants from 2 to 24 inches tall may be attacked. In conventional corn,
damage is usually confined to weedy border rows along fences, grass waterways and contour strips,
while weedy no-till fields may have damage throughout.
Plants damaged by stalk borers are often stunted and/or misshapen and may die. Infested plants (if
they survive) may or may not produce harvestable ears. If they do, ears are usually smaller than
normal. Those plants that do not produce ears compete with productive plants for water, nutrients and
sunlight.
Pest Identification
https://www.extension.purdue.edu/extmedia/BP/BP-96-12-W.pdf
“Purdue Extension Publication .” D I S E A S E S O F C O R N , 2012, pp. 1–5.
Corn trade is the largest contributor to the United States’ (US) agricultural trade balance, with the US
providing over half of the total supply of corn in the world market (USDA 2014). Field corn accounts
for over 87 million acres of land harvested within the US, contributes about $75 billion to the
economy, and comprises 95.4% of the total US feed grain production (NASS 2013; USDA 2015). In
short, corn is vitally important to the US agricultural and food economies, and ensuring a sustainable
supply of quality corn is critical in the years to come; not only for the United States, but for the global
food supply.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4815912/
Mitchell, N.J., et al. “Potential Economic Losses to the USA Corn Industry from Aflatoxin
Contamination.”Advances in Pediatrics., U.S. National Library of Medicine, Mar. 2016,
www.ncbi.nlm.nih.gov/pmc/articles/PMC4815912/.
Since the advent of farming, people have searched for ways to save their crops from insect pests. Even
ancient farmers were known to have collected seeds from high-yielding plants in the hope of
producing crops the next year that could withstand insect infestation.
Bt, or Bacillus thuringiensis, is a modern solution to insect control.
Bacillus thuringiensis (Bt) is a bacterium that occurs naturally in the soil and produces proteins that
kill certain insects. Through biotechnology, scientists can use these naturally occurring Bt proteins to
develop insect-protected crops that help farmers protect against insect damage and destruction. When
targeted insects eat the plant containing the protein, they ultimately die; but Bt is not harmful to
humans, other mammals, birds, fish, or beneficial insects.
Farmers can help prevent insect resistance through Insect Resistance Management (IRM)
practices.
Farmers who choose to grow a Bt crop must plant a “refuge”—a block or strip of the same crop that
does not contain a Bt trait, or the non-Bt refuge seed can be included in an EPA-approved seed blend
product, which we refer to as “Refuge in the Bag” or RIB. The insects from the refuge are not
exposed to the Bt protein and susceptible insects will survive, potentially mating with resistant insects
from the neighboring field. This practice is known as Insect Resistance Management.
https://monsanto.com/company/media/statements/insect-resistance-bt/
“Insect Resistance To Bt Crops.” Monsanto, Monsanto, 11 Apr. 2017,
monsanto.com/company/media/statements/insect-resistance-bt/.
Problems with insecticides have spurred the search for alternative means of insect control. Not only
do conventional insecticides cause environmental and safety hazards, more than 500 species of pests
have evolved resistance to them. Insecticidal proteins from the common bacterium Bacillus
thuringiensis (Bt) are an environmentally friendly alternative to conventional insecticides.
Bt toxins kill insects by binding to and disrupting midgut membranes. Unlike broad spectrum
insecticides, Bt toxins kill certain pests but cause little or no harm to most nontarget organisms
including wildlife, insect natural enemies, and people. For decades, sprays containing Bt toxins have
been useful in organic and mainstream pest control.
Transgenic crops that produce Bt toxins control some key pests, thus decreasing reliance on
insecticide applications1. Surprisingly, after seven years of large scale planting of Bt crops, pest
resistance to Bt crops in the field has not been documented 2.
Large scale planting of Bt crops began in 1996 and grew quickly to more than 10 million ha per year.
The cumulative area of Bt crops grown globally from 1996 to 2002 exceeded 62 million ha, enough to
cover the states of California and Iowa. More than 99% of this area was planted with either Bt corn or
Bt cotton producing Bt toxins Cry1Ab or Cry1Ac to kill larvae of lepidopteran pests. These Bt crops
expose pests to Bt toxin throughout the growing season.
The widespread and prolonged exposure to Bt toxins represents one of the largest selections for
resistance in insects the world has ever seen. Before Bt crops were grown commercially, many
scientists predicted that pests would evolve resistance quickly. This view was supported by pervasive
resistance to conventional insecticides, lab-selected resistance to Bt toxins in many pests, and field-
evolved resistance to sprays of Bt toxins in diamondback moth (Plutella xylostella)3.
To counter the threat of resistance, the refuge strategy 4 has been adopted widely. Growers provide
refuges of non-transgenic host plants along with Bt crops to enhance survival of susceptible pests.
Ideally, rare resistant adults emerging from Bt crops mate with more abundant susceptible adults from
refuges. Modeling results suggest that resistance can be substantially delayed if the heterozygous
offspring from such matings are killed by the Bt crop. The refuge strategy is based primarily on
theoretical calculations and limited experimental evidence from small-scale experiments with
diamondback moth. No rigorous large scale tests of the refuge strategy have been reported.
Although the refuge strategy works beautifully in theory, some scientists thought that real world
deviations from its assumptions could doom Bt crops to early failure. Contrary to this expectation,
researchers from the University of Arizona, the University of California, and Cornell University
recently reported that field-evolved resistance to Bt crops has not been documented yet 2. This
conclusion is based on a review of published results of resistance monitoring efforts in the U.S. and
China, which account for the vast majority of Bt crops grown worldwide. To enhance understanding
of this surprising outcome, we review below the status of pest resistance to Bt crops, including
responses of resistant strains in laboratory and greenhouse tests, and frequencies of resistance in field
populations targeted by Bt crops.
https://www.cornpest.ca/research/insect-resistance-to-bt-crops-lessons-from-the-first-seven-years/
“Home.” Canadian Corn Pest Coalition, Bruce E. Tabashnik, 2018, www.cornpest.ca/research/insect-
resistance-to-bt-crops-lessons-from-the-first-seven-years/.
How it is made
Bt corn is a type of transgenic crop because it contains a gene that has been artificially into it instead
from the process of pollination. The special gene of interest that was inserted into it is called a
transgene. The gene from Bacillus thuringiensis that produces thecrystal toxin protein has been
inserted into the D.N.A. of the corn and therefore making it poisonous to insects.
There are primarily 5 steps in creating transgenic crops like Bt corn:
Step1: Extracting the desired gene from other organism.
Step 2: cloning the desired gene of interest
Step 3: Designing the gene
Step 4: Transformation process
Step 5: Plant breeding.
Click here for an animation of the overview of Genetic Engineering in transgenic crops
Step1: Extracting the desired gene from other organism.
This step is the most limiting step in transgenic process because there is only limited information
known about specific genes required to enhance the characteristics of plants. Most of the research that
is now done is focused on the identification and sequencing of certain genes. Never the less isolation
of a specific gene can be easily explained and understood. First of all the main tools that are involved
in this process are restriction enzyme and D.N.A. ligase(www.user.rcn.com). Restriction enzymes are
enzymes that recognize a specific sequence of nucleotide bases on the D.N.A. and then cleaves it a
specific sequence. Each restriction enzyme is specific to a certain sequence of nucleotide bases
therefore one the sequence is known for the gene then the specific restriction enzyme is used. The
restriction enzymes are like scissors and then D.N.A. ligase is the glue that sticks back the ends of the
nucleotide sequences. Therefore it is used after the restriction enzyme to attach the parts of the D.N.A.
fragments together. The next step is to amplify the amount of D.N.A. that was obtained because a
significant amount is needed to be inserted into the desired organism.
Step 2: Cloning the desired gene of interest
The desired gene that was extracted is now subject to a process called polymerase chain
reaction(PCR), a method that is used to amplify the amount D.N.A. to a workable amount. Now the
D.N.A. is placed into the plasmid of the bacteria and is replicated to produce more of the D.N.A. At
this point an antibiotic resistant gene is also inserted into the plasmid which allows the carrier cell to
be amplified successfully through the process of transformation. The process of transformation
involves the carrier cells to be placed into two medium; one that has a specific antibiotic mean the
other has no antibiotic. The bacteria is then subject to the first medium whereby it is growth is
significant and then subjected to the other medium whereby only the bacteria that has the antibiotic
resistant gene can grow. The bacteria that are antibiotic resistant carries the desired D.N.A. in it and
therefore only that specific kind can grow, ensuring that all of the carrier bacteria will have the
desired trait.
Step 3: Designing the gene
This process is necessary because the gene has to undergo several modifications for it to be
effectively inserted into a plant. Below is a diagram of what parts must be added to the gene.
The promoter sequence must be added for the gene to be correctly placed into the D.N.A. of the plant.
The promoter works as an on/off switch that controls when and where in the plan the gene will be
expressed. The most common promoter is the CaMV35s which comes from the cauliflower mosaic
virus and cause the gene to be expressed throughout the life cycle of the plant in most tissues. On the
other hand other promoters are more specific and only respond in the plants during specific internal
and external environment. Sometimes the cloned gene is modified so that the plant enhances
production of the gene in its cells. This enhancement is done in the Bt corn, whereby the plants
nucleotide G-C is replaced with the A-T nucleotide from the Bacillus thuringiensis.
The other two parts that are added onto the gene is the termination sequence and a marker gene. The
termination sequence tells the cellular machinery when the end of the gene sequence has been
reached. The marker genes functions are to aid in identification of plants cells that have the specific
integration of the transgene. This process is necessary because only a small percentage of targeted
tissue will have the transgene. The marker gene usually consists of a protein that encodes for
resistance against herbicides or specific antibiotics.
Step 4: Transformation process.
Transformation in this process means the change that will be brought upon a cell through introduction
of a new D.N.A. There are two method how this could be achieved and it is explained below.
· This first method is the gene gun method where a gun is used to insert the D.N.A. This process
is also known as the micro-projectile bombardment method. This gun made up of a 6” x 7” x 10”
stainless steel chamber that is connected to a 2HP vacuum pump. Then the twitch is flicked on the
gun, helium is released at 1000 psi and disrupts a disk about the size of a nickel. The sock way travels
to another dish that has microscopic tungsten particles 1 micron in diameter which is coated with the
D.N.A. molecules. These particles travel 1300 feet per second and penetrate the cells and release the
D.N.A into the nucleus. It is then incorporated by the chromosomes of the plant and comes present in
the D.N.A. structure of the plant. For an animation of the gene gun click here.
·
The other method is with the Agrobacterium bacteria also known as Agrobacterium tumefaciens.
This bacteria is able to infect plant cells with a piece of its D.N.A. which cause tumors. Scientist have
genetically engineered this bacteria so that the gene responsible for tumor is no longer present and is
replaced by the gene that is to be inserted into a plant. This plasmid is activated by the plant when it is
wounded because the plant then releases chemical signals that activates it. When it is activated it
enters the plant through the wound and unfortunately this is not known how the D.N.A. from moves
to the cytoplasm to the nucleus of the plant. This process is beneficial because a large fragment of
D.N.A can be transferred effectively.
Step 5: Plant breeding
After all of the following process has occurred successfully a process known as tissue culture is used
to obtain the whole plant. In this process the plant tissues are grown under controlled environment in a
series of medium that contain specific nutrients and hormones. Also tests are carried out to ensure that
the plants have the desired gene and to see the activity and inheritance of the gene.
http://whatisbtcorn.pbworks.com/w/page/12449526/Biochemical%20Explaination%20of%20Bt
%20Corn
“Biochemical Explaination of Bt Corn.” What Is Bt Corn? / Economic Impact, Javier Vromero , Dec.
2009, whatisbtcorn.pbworks.com/w/page/12449526/Biochemical%20Explaination%20of%20Bt
%20Corn.
https://www.ncbi.nlm.nih.gov/pubmed/16779644
Wu, F. “Mycotoxin Reduction in Bt Corn: Potential Economic, Health, and Regulatory Impacts.” Advances in Pediatrics.,
U.S. National Library of Medicine, June 2006, www.ncbi.nlm.nih.gov/pubmed/16779644.