Scientists seek answers to food production problems
Some answers have been provided as interventions to some food production issues. Wish you happy reading
Introduction
Many factors can compromise the quality and/or safety of a food product. But one of the most common scenarios that faces a manufacturer is an unexpected problem that comes with a change of supplier.
The irony is that everything seems fine when the ingredient is received. It meets its specification (and this is similar to the previous supplier’s), yet nonetheless, the finished product ends up being far from satisfactory. The problem might be one of flavour, appearance, performance or smell, but whatever it is, the challenge is to find out what has changed as a consequence of changing the supplier, and to take steps to put things right.
Analytical approaches to problem solving
Some problems stand out such as a bad smell, the wrong colour, failure of performance, or presence of foreign bodies. Other problems may not be so obvious e.g. microbial spoilage, adulteration, inauthentic ingredients.
However, whether obvious or not, every problem must be investigated. There are a range of analytical techniques to help find out what has gone wrong and to inform what needs to be done to correct it.
Few manufacturers will have all of these techniques available on-site, so are likely to need to outsource some or all of the investigative work to a specialist laboratory. It makes a lot of sense to find a laboratory to partner with well in advance of a problem occurring, so that they are better able to assist when a problem arises!
Potential problems:
Appearance/foreign body
Blemishes and discolouration may be the result of chemical contamination or perhaps microbial spoilage; their investigation will likely involve the chemical techniques referred to in the discussion of taints (below). Other cosmetic/aesthetic problems such as sediments or a visible separation of emulsions, will be investigated by the physical techniques applicable to performance problems (also below).
Foreign bodies are a separate case. They can be broadly classified as extrinsic or intrinsic: The former come from external sources either by deliberate or accidental means. Intrinsic foreign bodies include ingredients such as a leaf or stalk, or an ingredient in an unusual/unexpected state.
A broad spectrum of technologies are routinely used in foreign body investigations, but simple light microscopy is often the starting point. It can be used to determine features that are typical or characteristic of the likely source, thereby directing scientists to the sophisticated methods that will provide confirmation.
Different techniques are required for different types of contaminant. For example, a scanning electron microscope fitted with an energy dispersive X-ray (EDX) detector is useful for identifying the elemental composition of items such as metal fragments. Plastic fragments, which may look like glass, require confirmation using a technique known as Fourier transform – infra red spectroscopy (FT-IR).
Taste/smell
An inappropriate taste or smell (or discoloration) in a product is usually due to the unexpected/unwanted presence of any number of chemicals. Or there may be an absence of key ingredients (e.g. bitterness blockers), or failure of a taste-masking system (e.g. encapsulation of oils), that might otherwise be expected to keep the unwanted flavours in check.
Taints can come from direct contamination, packaging or the airspace in a bottle/jar. The unwanted chemical may come from microbial spoilage, or perhaps from reaction of ingredients within the product.
Isolating and identifying a tainting chemical is often a challenge because certain taints can be very potent at very low concentrations (e.g. 20 parts per trillion). It depends on the product they are found in but chemicals like halo-anisoles and benzene are especially potent. Whilst certain groups or families of chemicals give rise to specific flavours/odours that an experienced chemist will recognise, there are thousands of potential tainting chemicals in widespread use, so there is never one obvious candidate.
A taint or off-flavour can originate at any point in the lifetime of a product, from production of the raw materials through to eventual consumption. Hence it may be necessary to trace the source of a taint back to any point in the supply chain.
Investigations will usually involve an initial assessment by human senses. If the offending chemical is believed to be organic (i.e. carbon-based) there will follow a chemical extraction procedure, separation via chromatography (either liquid or gas) and identification of the chemical using mass spectrometry or possibly nuclear magnetic resonance (NMR) spectrometry. A metallic contaminant will be detected using inductively coupled plasma (ICP) mass spectrometry or ICP-optimal emission spectroscopy.
This simple description belies the complexity that might be involved. As noted above, taints can be present in ppt concentrations. There is huge skill involved in extracting the taint, at detectable levels, free of other chemicals that might interfere with the analysis, and (in the case of volatile odours) without simply losing the chemical to the atmosphere before it can be identified.
Performance
Problems with the flow of liquids and semi-solids can be investigated using rheological instruments. These instruments apply different shearing forces which can mimic how materials might flow against different surfaces and internally. Such measurements will inform manufacturers of potential processing problems (e.g. when pumping) as well as problems with the behaviour of finished products. The resistance to flow by powders within hoppers, for example, can lead to clogging, or an accumulation of out-of-date material. The propensity for powders to behave in a disadvantageous manner can be predicted via a combination of powder rheology (Shear cell), particle sizing and microscopy.
Performance issues often come down to a problem with particle sizes or shape, as with the instability of an emulsion, or the gritty mouth feel of a product. This can be investigated using laser diffraction instruments, often in combination with microscopy techniques. The size and shape of particles can also be measured using static image analysis, which is a useful alternative to manual microscopy.
It is sometimes possible to observe how ingredients are distributed within a product by using X-ray tomography techniques along with the scanning electron microscope. This can give useful information about why a product performs badly. Even simple light microscopy, used with staining procedures can identify some of the microstructural features that are giving rise to performance problems.
The modern laboratory also has access to a range of instruments that can load products with crushing or stretching forces to investigate structural weaknesses (or strength).
Customer complaint/illness
Customers may attribute illness to a particular food item that shows no other signs of being at fault. Clearly, a manufacturer will want to investigate a complaint of this kind, with the possibility of allergen or pathogen contamination being a particular cause for concern.
Microbiological testing can address the latter, however allergen testing can be more complicated. As such, much depends on the nature of the complaint and the likelihood, or otherwise, that specific allergens might have come into contact with the product or its ingredients/packaging.
Tests for allergens usually rely on enzyme-linked immunosorbent assay (ELISA) techniques directed at specific proteins, or DNA techniques that can detect trace amounts of DNA associated with allergenic ingredients. In both cases, but especially with ELISA, it is important to be aware of the potential for interferences inherent to biological assays that can lead to false positive or false negative results. A laboratory must have robust protocols in place to reduce the risk of any false results.
Authenticity/purity
High profile scandals (horsemeat in beef, melamine in milk) remind us that the food supply chain is extremely complex and global, and tracing the origin of ingredients is near impossible. Moreover, not every player in the supply chain is necessarily honest or legitimate.
Whether there has been a specific incident, notification of a wider industry-concern or merely a desire on behalf of the manufacturer to protect their interests (perhaps with a new supplier), there are analytical approaches that will assist in determining the authenticity of a particular supply. However, this is very much dependent on the ingredient in question and authenticity is not always easy to prove.
Testing for authenticity in the case of meat and fish is relatively routine, using DNA methods that can target gene sequences found in one species but not in another. However the quantification of cross contamination in meat against the level set by the FSA still requires specialist knowledge and testing.
Other authenticity issues are more complex. For example, olive oil has well defined acceptable ranges for a variety of naturally occurring compounds giving the analyst a set of parameters that can be measured to assess authenticity.
Other techniques such as isotope ratio analysis have become established but these depend on building a large database of samples, at considerable cost. So new approaches such as non-targeted screening (NTS) are now being applied. Rather than looking for specific chemical compounds, analysts are applying chemo-metric or food-omic approaches to identify differences between samples and a dataset of known authentic ingredients. This ‘probabilistic’ approach to testing is useful for identifying ‘outliers’, allowing analysts to focus on the suspect samples more easily, and to devote time to more careful scrutiny of these.
Where adulteration is suspected, new methods may need to be developed as a matter of urgency to address the specific problem. In the melamine in milk example, a nitrogen-rich chemical had been added to milk to fool a test that judged quality by nitrogen content. That particular test had no means of detecting the source of nitrogen, and an entirely different way of testing milk was needed for this fraud to come to light.
Conclusion
It is impossible to give a definitive list of problems and solutions, even in a very broad sense. Each problem needs to be assessed and investigated on its own merits.
It is also impossible for every manufacturer to equip itself with the resources and expertise that would be needed to investigate every potential problem. Rather every manufacturer should seek to partner with an expert laboratory that understands its processes, and can work with them to highlight potential weaknesses, and understand vulnerabilities.
At least this approach will ensure that when a problem does occur, whatever it happens to be, there is help at hand to identify what has gone wrong, and recommendations on what needs to be done to put it right.
Source=http://www.foodqualitynews.com/Product-Categories/Audit-and-Certification/Scientists-seek-answers-to-food-production-problems
New Health Risks of GM Mosquitoes and Salmon ??
Just when genetically modified (GM) mosquitoes got their approval by the Cayman Islands and the government of Canada’s Prince Edward Island is trying to approve GM salmon, new research reveals unexpected and potentially dangerous effects of genetic engineering. Unfortunately, neither the makers of genetically modified organisms (GMOs) nor their regulators conduct the studies that are necessary to protect the public. Being bitten by GM mosquitoes and eating GM salmon remains a serious gamble.
The new discomfiting research published in Nature Methods[1] examined the unintended impacts of gene editing on the DNA of mice. Gene editing is touted by its promoters as the safer, more precise version of genetic engineering. The earlier version that was used to create the GM crops we all know about (soy, corn, etc.) forced genetic material from bacteria or viruses into plant DNA. Gene editing, on the other hand, does not necessarily introduce genes from foreign species. Rather, it cuts the DNA in a predetermined location. The cell’s DNA repair mechanisms are then activated to repair the cut.
Of all the gene editing techniques, the one that is easiest, least expensive, and most popular is called CRISPR-Cas9. Proponents claim it is so safe and predictable, it should not be regulated. They want to put their gene-edited products on the market without informing governments or consumers. And they don’t even want it to be called genetic engineering, since consumers have largely weighed in against GMOs. That is why the recent research is so damning.
Gene Editing Creates Predictable Mutations
The tools used for gene editing are designed to recognize and make changes only on specific DNA sequences. In the Nature Methods research, for example, the engineers designed their tools to fix a defective DNA sequence that could restore sight to blind mice. But the defective DNA sequence that governs sight is also repeated in other places throughout the mouse genome—unrelated to vision. Therefore, the gene editing tools can also make unintended changes in these “off-target” locations.
The unwanted mutations do not come from cutting the DNA. Rather, they occur when the cut ends are rejoined by the cells’ repair mechanisms. It results in either the loss of some DNA base units or the insertion of a few base units at the cut site.
If the mutation occurs in the middle of a known gene (or in a portion of the DNA that controls a gene) it can severely disrupt its function. Gene editors, therefore, rely on computer models of the genome to identify where the similar sequences are that are likely to become mutated and to predict what level of collateral damage that could create. If the risk is considered low enough, they proceed with editing.
Widespread Unpredicted Mutations Discovered
There is a joke that says molecular biologists don’t understand just two things: molecules and biology. Too often, the complex 3-D world doesn’t cooperate with their computer model predictions. This was again confirmed by the work of Stamford’s Dr. Kellie Schaefer, along with her colleagues from Stamford, Columbia, and the University of Iowa.
Instead of letting the computer guess which off-target changes would take place, Schaefer’s team actually sequenced the genome of the two gene-edited mice after they had undergone CRISPR-Cas9. They did find insertions and deletions (indels), which is the type of mutation that the computer predicts. One mouse had 164 indels; the other 128. But of the top 50 sequences that a computer would identify as most likely to be mutated, none were changed at all. Far more importantly, however, the computer model would totally miss their other finding: point mutations throughout the genome. One mouse had 1,736; the other 1,696.
A point mutation is the replacement of a single nucleotide along the DNA. But don’t let its smallness fool you. These so-called single-nucleotide variants (SNV) can have huge consequences. They can lead to many types of changes, including disease.
According to Dr. Michael Antoniou, a London-based molecular geneticist who routinely uses genetic engineering in his research, “Many of the genome editing-induced off-target mutations [both the point mutations and the indels] . . . will no doubt be benign in terms of effects on gene function. However, many will not be benign and their effects can carry through to the final marketed product, whether it be plant or animal.”[2] This could translate into possible toxins, allergens, carcinogens, or other changes that could affect those eating a GMO.
Dr. Michael Hansen, a Senior Scientist at Consumers Union, the policy arm of Consumer Reports, wrote, “While genome editing has been portrayed in the media as an incredibly precise process, where one can go in and literally only intentionally change one or a small number of nucleotide bases, the reality is that there can be large numbers of off-target effects.” He says, “This study raises troubling concerns.”
Another recently published study in Nature Communications used CRISPR/Cas9 to make 17 edits in the mouse genome. They too sequenced the genome and found unexpected insertions and deletions in all 17 places. Whereas deletions of approximately 9 base pairs are predicted, the actual size of the deletions was as high as 600 base pairs. No computer model predicts DNA damage this extensive.
A third study published this year[5] also found deletions of more than 500 base units. The researchers also confirmed that proteins produced by these mutated sections were altered. Such changes could theoretically transform a beneficial protein to a harmful one.
Hansen says the long deletions of DNA material “may not be routinely identified without whole genome sequencing.” But whole genome sequencing is rarely done by gene editors. Instead, they rely on their computers.
Even if they did sequence the genome, science doesn’t yet have the capacity to predict what the real-life consequences of all the mutations would be. Therefore, according to Antoniou, “it is also essential to ascertain the effects of these unintended changes on global patterns of gene function.” For this, both Antoniou and Hansen (as well as the National Academy of Sciences[6] and the international standard setting body Codex Alimentarius[7]) agree that the scientists must also analyze the changes in RNA, proteins, and metabolites.
Armed with this data, certain problems would be obvious—an increase of a known allergen or toxin, for example. But even if no red flags are raised at this point, according to Antoniou, “it is still necessary to conduct long-term toxicity studies” using animals. That’s because, once again, science is still not competent to figure out the complex interactions and side effects that can occur.
Antoniou concludes, “In the absence of these analyses, to claim that genome editing is precise and predictable is based on faith rather than science.”
And it is mere faith that supports the claims that GM mosquitoes and salmon are safe. Although they were not produced by the CRISP-Cas9 technique, they are the product of earlier gene-insertion techniques, which are also fraught with unpredictable mutations and altered gene expressions.
Earlier Research Warnings Ignored by GMO Makers
Just because this year’s research on gene editing shows unintended and potentially dangerous side effects does not mean that companies using the technology will change the way they operate. Indeed, back in 1999, a study showed widespread changes in the DNA due to gene insertion; but many GMO companies conveniently ignored the findings and continue to do so.
In that study, scientists studying cystic fibrosis inserted a gene into human cells.[8] Using a microarray, they discovered that the insertion “significantly affect[ed] up to 5% of the total genes in the array.” This means that the presence of a single foreign gene might change the expression of hundreds, possibly thousands of genes. In the case of the human cell being studied, the scientists were at a loss to determine the impact. “In the absence of more biological information,” they wrote, “we cannot discern which directions are better or worse, since any of these may have positive or negative effects.”
Just like the recent gene editing studies, this 1999 discovery contradicted the assumptions of an entire industry, which marched forward on the false assumption that their GMOs were predictable and safe.
The Untested Danger of a GM Mosquito Bite
In January 2014, I testified at the Florida Keys Mosquito Control District, opposing their planned release of GM mosquitoes. Also testifying was Derric Nimmo, a principal scientist at Oxitec, the UK company that produces the mosquitoes.
Oxitec had already conducted limited releases with millions of Aedis Aegypti mosquitoes in the Cayman Islands, Brazil, Panama, and Malaysia. The male insects were engineered to mate with natural females and produce offspring that die before reaching adulthood. Their plan was to reduce the population and thereby reduce the incidence of dengue and other diseases that this type of mosquito carries.
The company had widely publicized that they were only releasing males, which don’t bite. But it turns out that their method of sorting males from females is flawed, and thousands of biting female mosquitoes are released.[9] In addition, their method to create non-viable offspring is also flawed. Between 3%-15% of the offspring survive and prosper.[10] This can easily translate into millions of biting females, born from a genetically engineered family tree.
After the Florida hearing was over, I asked Derric if they ever analyzed the saliva from their GM mosquitoes, since the saliva enters the bloodstream of the people who are bitten. He said that they were just now doing research to see if the protein produced by the inserted gene was found in the saliva.
Realizing that they had already exposed the population of four countries to their mosquito saliva before doing this research, I was unimpressed. Then…
I explained to Derric the findings of the cystic fibrosis study, showing that a single inserted gene can create widespread changes, including new toxins, allergens, or carcinogens. Shouldn’t his company analyze everything in the saliva, I asked? Derric responded, “Good idea.”
ln Derric’s defense, Oxitec is not the only company that is tampering with nature’s gene pool in spite of the fact that it is wholly unprepared and unqualified to do so. Other GMO makers also fail to use the modern molecular profiling techniques that reveal unintended side effects. However, when independent scientists conduct that type of research on GMOs, the results are sobering.
For example, long after Monsanto’s Roundup Ready corn had been consumed by hundreds of millions of people, a team led by Dr. Antoniou[11] found more than 200 significant changes in its proteins and metabolites, compared to non-GMO corn of the same variety. Two of the compounds that increased are aptly named putrescine and cadaverine, because they produce the horrific smell of rotting dead bodies. More worrisome; they are also linked to higher risks of allergies and cancer. Another Monsanto GM corn has a new allergen[12] and their cooked soy has up to seven times the level of a known soy allergen, compared to cooked non-GMO soy.[13]
The Typical Biotech Response: Ignore or Attack
If regulators and medical authorities knew in advance that a proposed GMO contained new or higher levels of dangerous allergens, it is unlikely that the GMO would have been introduced. (I’m being optimistic.) But once a GMO variety is released, grown on millions of acres and eaten by millions of people, somehow the crop enjoys a bizarre immunity. Confronted with hard evidence of allergens, GMO makers and government regulators typically ignore the problem. The offending GMOs are still on the market, and they don’t carry any warnings on the package to protect those who might react.
If independent scientists discover an adverse finding that might threaten their bottom line, companies like Monsanto enlist a veritable army of supporters to drum up opposition—often using unscientific excuses that are repeated so often that they appear to be facts.
Two gene-editing companies whose stocks plummeted after the Nature Methods article came out quickly mounted their attack. But according to GMWatch.org, “the findings reported in the article, along with other recent research papers that also report unintended effects of CRISPR gene editing, show that the companies are arguing on the wrong side of the science.”[14]
The main argument used by the company Intellia was that the mutations were not from the gene editing at all. They claim that “the more plausible conclusion is that the genetic differences reflect a normal level of variation between individuals in a colony.”[15] But the scientific literature does not support this conclusion, given that:
1. Most of the mutations (117 indels and 1397 SNVS) were exactly the same in the two mice. According to GMWatch.org, “This indicates a targeted and non-random process.” If it were “a normal level of variation,” as Intellia insists, there would be much greater difference between the mice.
2. Another study looked at the genomes of 36 different strains of mice. None of the point mutations that were found in the gene-edited mice were in any of these strains. Thus, they don’t appear to be naturally occurring at all.
3. In fact, the sheer number of mutations in the edited mice was higher than scientists find among natural strains.
Perhaps the most strained logic used by Intellia to attack the research was that “there is no known mechanistic basis for Cas9 to induce SNVs.” In other words, the journal should not have published research showing unpredicted changes in the DNA simply because no one yet has figured out why those changes take place.
But if these widespread mutations exist in Crispr-Cas9 edited organisms, according to Antoniou they are likely happening with all the new gene editing techniques, which haven’t yet been studied in such detail.
Real Dangers and Perceived Dangers are Both Dangerous
If we apply these lessons to GM mosquitoes, there are serious consequences. If the saliva contains a new toxin or allergen, it might elicit mild or even deadly reactions. Since there are no human clinical trials and no public health surveillance related to the mosquito, the cause of any associated health problems could go unnoticed. It would require a large-scale outbreak of a serious reaction for health authorities to even mount an investigation, let alone consider the mosquito as a potential source.
Whether or not the GM mosquito causes harm, there is another problem that the Cayman authorities have surely overlooked. Suppose a girl who is vacationing on the island has a sudden onset of a serious health issue without an apparent cause. And suppose that her parents notice that she has also been bitten by mosquitoes. Now suppose that they draw the conclusion, correctly or incorrectly, that her condition is caused by the bite of a GM mosquito and that story is picked up by the media.
It doesn’t have to be a prominent media source for it to inspire some supermarket tabloid to dream up alarming headlines about the serious threat to American tourists by deadly engineered mosquitoes. The results could be disastrous for Cayman tourism.
The Cayman government is not only gambling that GM mosquitoes are safe (which cannot be guaranteed at this point), but also that no one draws the conclusion that they got harmed from being bitten by one. Who would want to vacation on an island where a mosquito bite could lead to who knows what?
It’s the who-knows-what that is the main point here. No one knows. But now that we understand that the generic genetic engineering process that created the mosquito also creates unpredictable and potentially dangerous changes, who in their right mind would release them? Oxitec would, obviously. And they still haven’t published any research on the composition of their GM mosquito saliva.
Oxitec is also planning to release genetically engineered moths in upstate New York. The male moths, like the mosquitoes, mate with natural females and produce larvae that don’t make it to maturity. But that larvae will inevitably be deposited into cabbage, cauliflower, and broccoli. What if the genetic engineering process alters the larvae and creates a toxin or allergen? Eating that vegetable might trigger a reaction. And just like the mosquito bite, it would be hard to trace, and the perception of harm (real or unreal) could damage produce sales from regions near the moths’ release.
Oxitec is owned by Intrexon, which also owns AquaBounty—the maker of GM salmon. The research on the salmon did show indications of off-target effects, with higher amounts of a cancer promoting hormone (IGF-1) and larger allergenic potential. But the number of fish used in the study was so small that the changes were not statistically significant. On behalf of Consumers Union, Hansen wrote to the FDA, “Because FDA’s assessment is inadequate, we are particularly concerned that this salmon may pose an increased risk of severe, even life-threatening allergic reactions to sensitive individuals. Instead of approving this product, FDA should be requiring studies with data from many more engineered fish, not the tiny sample of six fish on which it currently bases its conclusions. Unfortunately, even the data from those six fish raises concerns.” The FDA did not heed Hansen’s warning and instead approved the salmon for consumption.
At this point, there are no comprehensive analyses or feeding studies on any of these Intrexon GMOs. Their release might not only affect human health, they can permanently alter the gene pool. If the salmon escape confinement into the ocean, if the surviving GM mosquitoes or moths persist, there is no technology on earth to recall them. Any side effect can be with us for generations.
Although GMO companies like to argue that GMOs with built-in sterility will not persist in the environment. Given the fact that a percentage can survive, however, their argument is deceptive. In addition, studies confirm that after several generations, genetically engineered traits in insects can fail. A recent study, for example, showed that newly introduced traits in engineered mosquitoes failed in just 25 generations.
Intrexon can’t pretend it doesn’t know about the dangers and problems with genetic engineering technology, both real and perceived. Robert Shapiro has been on their board since 2011. He was the CEO of Monsanto who arranged to fast track the release of GMOs into the food supply. Monsanto inserted the company’s attorney into the FDA, where he pioneered the policy that allows GMOs onto the market without a single adequate safety study. Since then, numerous studies have pointed to serious health impacts, all of which are ignored or attacked.
Many of us who study the research on GMOs are convinced that they contribute to rising disease rates in the US. But even if we’re wrong, no one can pretend that the GMOs have been safe for the economy. All over the world and especially in the US, consumer rejection of GMOs has exacted a heavy economic toll on food companies and agribusiness.
But even if the regulators in the Cayman Islands and Prince Edward Island are ignoring the trends, others are wising up. According to Friends of the Earth, “more than 79 grocery retailers with more than 11,000 stores have now made commitments to not sell the GMO salmon,”[18] if it gets introduced into the market. Major brands are already racing to eliminate derivatives of GM crops, even advertising on TV that their products are non-GMO. And many countries and regions that had considered Oxitec’s GM mosquitoes have said no and are opting for safer alternatives.[19] And as long new studies continue to demonstrate serious unpredicted side-effects from genetic engineering, more consumers will take the necessary precautions.
Source=http://www.huffingtonpost.com/entry/research-exposes-new-health-risks-of-genetically-modified_us_597a3cb4e4b06b305561cef3
Note=To safe space, some references are left out
Aug 6 2017
Is this TRUE …..GLYPHOSATE has effect on AUTISM ???
MIT Researcher: Glyphosate Herbicide will Cause Half of All Children to Have Autism by 2025
By Alliance For Natural Health
anh-usa.org
Why? Evidence points to glyphosate toxicity from the overuse of Monsanto’s Roundup herbicide on our food.
For over three decades, Stephanie Seneff, PhD, has researched biology and technology, over the years publishing over 170 scholarly peer-reviewed articles. In recent years she has concentrated on the relationship between nutrition and health, tackling such topics as Alzheimer’s, autism, and cardiovascular diseases, as well as the impact of nutritional deficiencies and environmental toxins on human health.
At a [recent] conference, in a special panel discussion about GMOs, she took the audience by surprise when she declared, “At today’s rate, by 2025, one in two children will be autistic.” She noted that the side effects of autism closely mimic those of glyphosate toxicity, and presented data showing a remarkably consistent correlation between the use of Roundup on crops (and the creation of Roundup-ready GMO crop seeds) with rising rates of autism. Children with autism have biomarkers indicative of excessive glyphosate, including zinc and iron deficiency, low serum sulfate, seizures, and mitochondrial disorder.
A fellow panelist reported that after Dr. Seneff’s presentation, “All of the 70 or so people in attendance were squirming, likely because they now had serious misgivings about serving their kids, or themselves, anything with corn or soy, which are nearly all genetically modified and thus tainted with Roundup and its glyphosate.”
Dr. Seneff noted the ubiquity of glyphosate’s use. Because it is used on corn and soy, all soft drinks and candies sweetened with corn syrup and all chips and cereals that contain soy fillers have small amounts of glyphosate in them, as do our beef and poultry since cattle and chicken are fed GMO corn or soy. Wheat is often sprayed with Roundup just prior to being harvested, which means that all non-organic bread and wheat products would also be sources of glyphosate toxicity. The amount of glyphosate in each product may not be large, but the cumulative effect (especially with as much processed food as Americans eat) could be devastating. A recent study shows that pregnant women living near farms where pesticides are applied have a 60% increased risk of children having an autism spectrum disorder.
Other toxic substances may also be autism-inducing. You may recall our story on the CDC whistleblower who revealed the government’s deliberate concealment of the link between the MMR vaccine (for measles, mumps, and rubella) and a sharply increased risk of autism, particularly in African American boys. Other studies now show a link between children’s exposure to pesticides and autism. Children who live in homes with vinyl floors, which can emit phthalate chemicals, are more likely to have autism. Children whose mothers smoked were also twice as likely to have autism. Research now acknowledges that environmental contaminants such as PCBs, PBDEs, and mercury can alter brain neuron functioning even before a child is born.
This month, the USDA released a study finding that although there were detectable levels of pesticide residue in more than half of food tested by the agency, 99% of samples taken were found to be within levels the government deems safe, and 40% were found to have no detectable trace of pesticides at all. The USDA added, however, that due to “cost concerns,” it did not test for residues of glyphosate.Let’s repeat that:they never tested for the active ingredient in the most widely used herbicide in the world. “Cost concerns”? How absurd—unless they mean it will cost them too much in terms of the special relationship between the USDA and Monsanto. You may recall the revolving door between Monsanto and the federal government, with agency officials becoming high-paying executives—and vice versa! Money, power, prestige: it’s all there. Monsanto and the USDA love to scratch each others’ backs. Clearly this omission was purposeful.
In addition, as we have previously reported, the number of adverse reactions from vaccines can be correlated as well with autism, though Seneff says it doesn’t correlate quite as closely as with Roundup. The same correlations between applications of glyphosate and autism show up in deaths from senility.
Of course, autism is a complex problem with many potential causes. Dr. Seneff’s data, however, is particularly important considering how close the correlation is—and because it is coming from a scientist with impeccable credentials. Earlier this year, she spoke at the Autism One conference and presented many of the same facts; that presentation is available on YouTube.
Monsanto claims that Roundup is harmless to humans. Bacteria, fungi, algae, parasites, and plants use a seven-step metabolic route known as the shikimate pathway for the biosynthesis of aromatic amino acids; glyphosate inhibits this pathway, causing the plant to die, which is why it’s so effective as an herbicide. Monsanto says humans don’t have this shikimate pathway, so it’s perfectly safe.
Dr. Seneff points out, however, that our gut bacteria do have this pathway, and that’s crucial because these bacteria supply our body with crucial amino acids. Roundup thus kills beneficial gut bacteria, allowing pathogens to grow; interferes with the synthesis of amino acids including methionine, which leads to shortages in critical neurotransmitters and folate; chelates (removes) important minerals like iron, cobalt and manganese; and much more.
Even worse, she notes, additional chemicals in Roundup are untested because they’re classified as“inert,” yet according to a 2014 study in BioMed Research International, these chemicals are capable of amplifying the toxic effects of Roundup hundreds of times over.
Glyphosate is present in unusually high quantities in the breast milk of American mothers, at anywhere from 760 to 1,600 times the allowable limits in European drinking water. Urine testing shows Americans have ten times the glyphosate accumulation as Europeans.
“In my view, the situation is almost beyond repair,” Dr. Seneff said after her presentation. “We need to do something drastic.”
Source=http://healthimpactnews.com/2014/mit-researcher-glyphosate-herbicide-will-cause-half-of-all-children-to-have-autism-by-2025/Source
Aug 6, 2017
SFFF Comments=We welcome your comments on this report urgently
World Conference 2018
World of Food Safety Conference
Please visit
https://10times.com/world-food-safety-conference
Food safety Conference ASIA 2018
Food Safety Asia
For more details
Please visit https://10times.com/food-safety-asia
Aug 1 2017
AFRICAN BIO-SCIENCES CHALLENGE FUND 2017-2018
The BecA-ILRI call for application to African Researchers is out
Closing date June 2018
Please visit
Some answers to food production problems
Scientists seek answers to food production problems
Some answers have been provided as interventions to some food production issues. Wish you happy reading
Introduction
Many factors can compromise the quality and/or safety of a food product. But one of the most common scenarios that faces a manufacturer is an unexpected problem that comes with a change of supplier.
The irony is that everything seems fine when the ingredient is received. It meets its specification (and this is similar to the previous supplier’s), yet nonetheless, the finished product ends up being far from satisfactory. The problem might be one of flavour, appearance, performance or smell, but whatever it is, the challenge is to find out what has changed as a consequence of changing the supplier, and to take steps to put things right.
Analytical approaches to problem solving
Some problems stand out such as a bad smell, the wrong colour, failure of performance, or presence of foreign bodies. Other problems may not be so obvious e.g. microbial spoilage, adulteration, inauthentic ingredients.
However, whether obvious or not, every problem must be investigated. There are a range of analytical techniques to help find out what has gone wrong and to inform what needs to be done to correct it.
Few manufacturers will have all of these techniques available on-site, so are likely to need to outsource some or all of the investigative work to a specialist laboratory. It makes a lot of sense to find a laboratory to partner with well in advance of a problem occurring, so that they are better able to assist when a problem arises!
Potential problems:
Appearance/foreign body
Blemishes and discolouration may be the result of chemical contamination or perhaps microbial spoilage; their investigation will likely involve the chemical techniques referred to in the discussion of taints (below). Other cosmetic/aesthetic problems such as sediments or a visible separation of emulsions, will be investigated by the physical techniques applicable to performance problems (also below).
Foreign bodies are a separate case. They can be broadly classified as extrinsic or intrinsic: The former come from external sources either by deliberate or accidental means. Intrinsic foreign bodies include ingredients such as a leaf or stalk, or an ingredient in an unusual/unexpected state.
A broad spectrum of technologies are routinely used in foreign body investigations, but simple light microscopy is often the starting point. It can be used to determine features that are typical or characteristic of the likely source, thereby directing scientists to the sophisticated methods that will provide confirmation.
Different techniques are required for different types of contaminant. For example, a scanning electron microscope fitted with an energy dispersive X-ray (EDX) detector is useful for identifying the elemental composition of items such as metal fragments. Plastic fragments, which may look like glass, require confirmation using a technique known as Fourier transform – infra red spectroscopy (FT-IR).
Taste/smell
An inappropriate taste or smell (or discoloration) in a product is usually due to the unexpected/unwanted presence of any number of chemicals. Or there may be an absence of key ingredients (e.g. bitterness blockers), or failure of a taste-masking system (e.g. encapsulation of oils), that might otherwise be expected to keep the unwanted flavours in check.
Taints can come from direct contamination, packaging or the airspace in a bottle/jar. The unwanted chemical may come from microbial spoilage, or perhaps from reaction of ingredients within the product.
Isolating and identifying a tainting chemical is often a challenge because certain taints can be very potent at very low concentrations (e.g. 20 parts per trillion). It depends on the product they are found in but chemicals like halo-anisoles and benzene are especially potent. Whilst certain groups or families of chemicals give rise to specific flavours/odours that an experienced chemist will recognise, there are thousands of potential tainting chemicals in widespread use, so there is never one obvious candidate.
A taint or off-flavour can originate at any point in the lifetime of a product, from production of the raw materials through to eventual consumption. Hence it may be necessary to trace the source of a taint back to any point in the supply chain.
Investigations will usually involve an initial assessment by human senses. If the offending chemical is believed to be organic (i.e. carbon-based) there will follow a chemical extraction procedure, separation via chromatography (either liquid or gas) and identification of the chemical using mass spectrometry or possibly nuclear magnetic resonance (NMR) spectrometry. A metallic contaminant will be detected using inductively coupled plasma (ICP) mass spectrometry or ICP-optimal emission spectroscopy.
This simple description belies the complexity that might be involved. As noted above, taints can be present in ppt concentrations. There is huge skill involved in extracting the taint, at detectable levels, free of other chemicals that might interfere with the analysis, and (in the case of volatile odours) without simply losing the chemical to the atmosphere before it can be identified.
Performance
Problems with the flow of liquids and semi-solids can be investigated using rheological instruments. These instruments apply different shearing forces which can mimic how materials might flow against different surfaces and internally. Such measurements will inform manufacturers of potential processing problems (e.g. when pumping) as well as problems with the behaviour of finished products. The resistance to flow by powders within hoppers, for example, can lead to clogging, or an accumulation of out-of-date material. The propensity for powders to behave in a disadvantageous manner can be predicted via a combination of powder rheology (Shear cell), particle sizing and microscopy.
Performance issues often come down to a problem with particle sizes or shape, as with the instability of an emulsion, or the gritty mouth feel of a product. This can be investigated using laser diffraction instruments, often in combination with microscopy techniques. The size and shape of particles can also be measured using static image analysis, which is a useful alternative to manual microscopy.
It is sometimes possible to observe how ingredients are distributed within a product by using X-ray tomography techniques along with the scanning electron microscope. This can give useful information about why a product performs badly. Even simple light microscopy, used with staining procedures can identify some of the microstructural features that are giving rise to performance problems.
The modern laboratory also has access to a range of instruments that can load products with crushing or stretching forces to investigate structural weaknesses (or strength).
Customer complaint/illness
Customers may attribute illness to a particular food item that shows no other signs of being at fault. Clearly, a manufacturer will want to investigate a complaint of this kind, with the possibility of allergen or pathogen contamination being a particular cause for concern.
Microbiological testing can address the latter, however allergen testing can be more complicated. As such, much depends on the nature of the complaint and the likelihood, or otherwise, that specific allergens might have come into contact with the product or its ingredients/packaging.
Tests for allergens usually rely on enzyme-linked immunosorbent assay (ELISA) techniques directed at specific proteins, or DNA techniques that can detect trace amounts of DNA associated with allergenic ingredients. In both cases, but especially with ELISA, it is important to be aware of the potential for interferences inherent to biological assays that can lead to false positive or false negative results. A laboratory must have robust protocols in place to reduce the risk of any false results.
Authenticity/purity
High profile scandals (horsemeat in beef, melamine in milk) remind us that the food supply chain is extremely complex and global, and tracing the origin of ingredients is near impossible. Moreover, not every player in the supply chain is necessarily honest or legitimate.
Whether there has been a specific incident, notification of a wider industry-concern or merely a desire on behalf of the manufacturer to protect their interests (perhaps with a new supplier), there are analytical approaches that will assist in determining the authenticity of a particular supply. However, this is very much dependent on the ingredient in question and authenticity is not always easy to prove.
Testing for authenticity in the case of meat and fish is relatively routine, using DNA methods that can target gene sequences found in one species but not in another. However the quantification of cross contamination in meat against the level set by the FSA still requires specialist knowledge and testing.
Other authenticity issues are more complex. For example, olive oil has well defined acceptable ranges for a variety of naturally occurring compounds giving the analyst a set of parameters that can be measured to assess authenticity.
Other techniques such as isotope ratio analysis have become established but these depend on building a large database of samples, at considerable cost. So new approaches such as non-targeted screening (NTS) are now being applied. Rather than looking for specific chemical compounds, analysts are applying chemo-metric or food-omic approaches to identify differences between samples and a dataset of known authentic ingredients. This ‘probabilistic’ approach to testing is useful for identifying ‘outliers’, allowing analysts to focus on the suspect samples more easily, and to devote time to more careful scrutiny of these.
Where adulteration is suspected, new methods may need to be developed as a matter of urgency to address the specific problem. In the melamine in milk example, a nitrogen-rich chemical had been added to milk to fool a test that judged quality by nitrogen content. That particular test had no means of detecting the source of nitrogen, and an entirely different way of testing milk was needed for this fraud to come to light.
Conclusion
It is impossible to give a definitive list of problems and solutions, even in a very broad sense. Each problem needs to be assessed and investigated on its own merits.
It is also impossible for every manufacturer to equip itself with the resources and expertise that would be needed to investigate every potential problem. Rather every manufacturer should seek to partner with an expert laboratory that understands its processes, and can work with them to highlight potential weaknesses, and understand vulnerabilities.
At least this approach will ensure that when a problem does occur, whatever it happens to be, there is help at hand to identify what has gone wrong, and recommendations on what needs to be done to put it right.
First published in 2016 by
Reading Scientific Services Limited
Source=http://www.foodqualitynews.com/Product-Categories/Audit-and-Certification/Scientists-seek-answers-to-food-production-problems
Aug 1 2017
DUBAI 2018-INTERNATIONAL CONFERENCE ON FOOD SAFETY AND SANITATION
SEPTEMBER 24-25 2018
Take advantage of this meeting and link up with experts across the world
Visit ==https://waset.org/conference/2018/09/dubai/ICFSS
Important Dates
Important Notes
Please ensure your submission meets WASET’s strict guidelines for accepting scholarly papers. Downloadable versions of the check list for Full-Text Papers and Abstract Papers.
Please refer to the Paper Submission GUIDE before submitting your paper.
Selected Conference Papers
1) Nutritional Value Determination of Different Varieties of Oats and Barley Using Near-Infrared Spectroscopy Method for the Horses Nutrition
V. Viliene, V. Sasyte, A. Raceviciute-Stupeliene, R. Gruzauskas
2) Nutrition and Food Safety as Strategic Assets
Daniel C. S. Lim, W. Y. Tan
3) Radiation Usage Impact of on Anti-Nutritional Compounds (Antitrypsin and Phytic Acid) of Livestock and Poultry Foods
Mohammad Khosravi, Ali Kiani, Behroz Dastar, Parvin Showrang
4) Factors Determining Selection of Essential Nutrition Supplements
Daniel C. S. Lim
5) Combinatory Nutrition Supplementation: A Case of Synergy for Increasing Calcium Bioavailability
Daniel C. S. Lim, Eric Y. M. Yeo, W. Y. Tan
6) Determining Food Habits in Süleymanpasa Town of Tekirdag City, Turkey
Emine Yilmaz, Ismail Yilmaz, Harun Uran
7) Nutritional Composition of Selected Wild Fruits from Minna Area of Niger State, Nigeria
John O. Jacob, Abdullahi Mann, Olanrewaju I. Adeshina, Mohammed M. Ndamitso
8) An Extended Model for Sustainable Food and Nutrition Security in the Agrifood Sector
Ioannis Manikas
9) Nutrition Program Planning Based on Local Resources in Urban Fringe Areas of a Developing Country
Oktia Woro Kasmini Handayani, Bambang Budi Raharjo, Efa Nugroho, Bertakalswa Hermawati
10) Food Security in the Middle East and North Africa
Sara D. Garduño-Diaz, Philippe Y. Garduño-Diaz
11) On the Combination of Patient-Generated Data with Data from a Secure Clinical Network Environment – A Practical Example
Jeroen S. de Bruin, Karin Schindler, Christian Schuh
12) Liability Aspects Related to Genetically Modified Food under the Food Safety Legislation in India
S. K. Balashanmugam, Padmavati Manchikanti, S. R. Subramanian
13) IT System in the Food Supply Chain Safety: Application in SMEs Sector
Mohsen Shirani, Micaela Demichela
14) Oat Grain Functional Ingredient Characterization
Vita Sterna, Sanita Zute, Inga Jansone, Linda Brunava, Inara Kantane
15) MEAL Project: Modifying Eating Attitudes and Actions through Learning
E. Oliver, A. Cebolla, A. Dominguez, A. Gonzalez-Segura, E. de la Cruz, S. Albertini, L. Ferrini, K. Kronika, T. Nilsen, R. Baños
Mycotoxin training opportunity in Bari, Italy, October 2017
ISM – MYCOKEY Workshop–Training Course “Rapid Methods for Mycotoxin Detection in the Food Chain” 9-13 October 2017, Bari, Italy
http://rapidmethods.mycokey.eu
The Institute of Sciences of Food Production – National Research Council of Italy (ISPA-CNR), under the aegis of the MYCOKEY project (http://www.mycokey.eu/) and the International Society for Mycotoxicology (ISM), is hosting a one-week Workshop-Training Course from October 9-13, 2017.
The course will give information about major issues associated with mycotoxin analysis and contamination along the food chain. Lectures and laboratory training will be provided on routinely used and new screening tools for rapid, robust and user-friendly analysis of mycotoxins, including validation aspects.
Practical training in the laboratory will cover most of the course and trainees will be assisted individually in the laboratory by ISPA-CNR staff expert in instrumental and immunochemical analysis of mycotoxins.
The Training course website is http://rapidmethods.mycokey.eu and the event has been disseminate also through the EU website (http://ec.europa.eu/research/index.cfm?pg=events&eventcode=6EC57A16-9DFE-3418-908C20CF8B6ECD33)
Aug 1 2017
Conference for Food Protection 2018
This Conference takes place in the USA in 2018. Get prepared and meet experts in analyses and certification
For more , please visit
http://www.foodprotect.org/
Food Technology Conference== France
19th International Conference on
Food Processing & Technology
Theme: Targeted Innovation to Nourish the Challenging World
For more information please visit
http://foodtechnology.conferenceseries.com/