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Daily Archives: July 28, 2017
Webster’s NanoRacks expands its role in commercial space – Houston Chronicle
Posted: July 28, 2017 at 6:49 pm
Photo: Steve Gonzales, Staff
Webster's NanoRacks expands its role in commercial space
An airlock destined for the International Space Station sat near the bottom of a 40-foot pool as astronauts hoisted bulky suits around its curvatures. NASA was testing the station's first complex fixture - an element that could one day be attached to a commercial space station - that is privately owned.
"If we're going to see an economy develop in low-Earth orbit the commercial sector has got to be able to provide and operate things like this," said Mike Read, manager of the International Space Station's commercial space utilization office.
That's the goal of Webster-based NanoRacks, which has evolved from getting experiments on the space station to developing an airlock that will help deploy satellites. Ultimately, NanoRacks hopes its roughly $12 million airlock will be detached from the government-owned space station and reattached to one that is commercially owned and operated.
"The goal of this is to continue to build the marketplace so there's more commercial users of ISS," said Brock Howe, NanoRacks' project manager for the airlock. "And then, at the point when the government is ready to retire the big space station, there are a lot of people using it that can then justify the price of having a commercial space station."
Read said the test in NASA's Neutral Buoyancy Laboratory in late June was standard for any new element being attached to the space station. NASA astronauts were testing handrail placements to ensure they could maneuver around the airlock during space walks.
To read this article in one of Houston's most-spoken languages, click on the button below.
This is just one of many tests the airlock will undergo before May 2019 when it's scheduled to hitch a ride to the International Space Station on the SpaceX Dragon.
"It's a big step for us to turn over operation of something as critical as an airlock," Read said.
NanoRacks and NASA signed a Space Act Agreement in May 2016 to begin development of the airlock. Nine months later, NanoRacks selected Boeing to develop the critical seal that connects the airlock to the space station. This device, called a Passive Common Berthing Mechanism, is essential for pressurizing the unit.
The airlock is about eight feet in diameter and will be five times larger than the space station's existing airlock. The existing airlock, in the Japanese Experiment Module, has a door for loading satellites and another door for ejecting them into space. NanoRacks' airlock will have only one hatch.
Astronauts will go inside the NanoRacks airlock while it's pressurized and arrange satellites. Once they leave, air is sucked out and the space station's robotic arm disconnects the airlock from the space station. The airlock is positioned away from the space station, and then satellites are deployed.
This design will allow NanoRacks to deploy larger satellites or several smaller satellites simultaneously. NASA will operate the robotic arm, and NanoRacks will deploy the satellites from its office in Webster.
"One of the big savings that NASA likes a lot is it will reduce crew time," Howe said. "Crew time is one of the most precious resources they have on station."
Payloads can also be attached to the airlock's exterior to hold experiments or cameras taking pictures of Earth.
Howe expects the airlock will be used four to six times a year, though that could change depending on demand.
"It's really going to be governed by the commercial marketplace," Howe said. "So if people want to use it, and scientists and experimenters want to use it, I think we will be able to use it more often. Because that's what ISS is trying to do. They're trying to embrace users of the space station."
Marco Caceres, senior analyst and director of space studies for Teal Group, said the company found "novel ways to make money in space, to make use of an incredible asset." Some people believe the space station hasn't been used to its fullest potential, and companies like NanoRacks could help change that.
Yet most commercial space efforts aren't focused on the space station, he said. Companies are more focused on launch vehicles and satellites because those are more obvious money makers. The space station could have an advantage if it provides a cheaper avenue for deploying satellites, Caceres said.
NanoRacks has found it is cheaper from the space station because it costs less to ride on a rocket bringing other cargo to the space station than on a rocket being launched solely for the satellites, Howe said.
NanoRacks must have 90 percent of the airlock's design completed by late October. It has already begun fabricating some parts, but that will pick up after October. NanoRacks is considering two vendors along the East Coast, and then those pieces will be shipped to Webster for assembly in NanoRacks' clean room.
"For NanoRacks to land that deal and to be able to accomplish what they've accomplished to date speaks volumes for this area and speak volumes for the commercial space industry," said Bob Mitchell, president of the Bay Area Houston Economic Partnership.
Looking ahead, NanoRacks is part of a team studying if rocket upper stages could be converted into space habitats. An upper stage is part of the rocket engine that is discarded in space after all of the fuel has been used.
Using these rocket components could be a more affordable way to create a commercial space station compared with building modules on the ground and launching them into orbit.
Ultimately, Howe said, NanoRacks wants to be involved if a commercial space station comes to fruition.
"Building a commercial space station will not be easy," he said. "There's lots of challenges ahead of the team to get that done. And we will see if the space industry can rise to the occasion and make it happen."
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Webster's NanoRacks expands its role in commercial space - Houston Chronicle
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Want to see the International Space Station over Lincolnshire? Here’s everything you need to know – LincolnshireLive
Posted: at 6:49 pm
Stargazers are in for a treat as the International Space Station is set to cross Lincolnshire's skies - and you don't need any equipment to see it.
The International Space Station (ISS) will be visible over Lincolnshire at various times between now and August 8 and 9.
And because of its enormous size you don't have to have a telescope to view it in the night sky as it'll be visible to the naked eye.
The ISS is more than 100m wide, over 70m long, and about 20m high. The orbital height (height above Earth) is just over 400km.
Get ready to see shooting stars! Delta Aquarid meteor shower will light up the skies this week
But you'll have to keep your eyes on the prize; the speed of orbit is so high 17,200mph that it will often only be visible for a few minutes at a time.
According to NASAs Spot The Station web site, the ISS looks like an airplane or a very bright star moving across the sky, except it doesnt have flashing lights or change direction. It will also be moving considerably faster than a typical airplane.
The station will be visible from all over Lincolnshire and North Lincolnshire, including Lincoln, Grimsby, Scunthorpe, Boston, Sleaford and Grantham, within a minute of the following dates and times:
July 28: 12.18am, 10.49pm
July 29: 12.25am, 9.57pm, 11.33pm
July 30: 1.10am, 10.41pm
July 31: 12.17am, 9.49pm, 11.25pm
August 1: 10.33pm
August 2: 12.09am, 9.40pm, 11.17pm
August 3: 10.24pm
August 4: 12.02am, 9.32pm, 11.09pm
August 5: 10.17pm
August 6: 9.24pm, 11.02pm
August 7: 10.08pm
August 8: 9.16pm
The International Space Station will always start passing from a westerly direction so keep your eyes peeled for it gliding across the sky.
Sometimes a pass can last as long as five minutes, but it looks like a bright, fast-moving star so be careful not to mistake it for a passing aircraft.
It takes 90 minutes to orbit so you may be able to catch it passing more than once if you dont mind spending a couple of hours outside at night.
For more information about the ISS, visit https://spotthestation.nasa.gov/home.cfm .
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Want to see the International Space Station over Lincolnshire? Here's everything you need to know - LincolnshireLive
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Astronaut Sunita Williams On Her Time In Space and ‘The Mars Generation’ – WBUR
Posted: at 6:49 pm
wbur
July 28, 2017
Sunita Williams, a native of Needham, has traveled far beyond Massachusetts as part of her work as an astronaut at the International Space Station. She served as the commander of the space station in 2012, and has spent a total 322 days in space. She also has spent more than 50 hours on space walks alone. She is featured in the new documentary film The Mars Generation, which looks at a new generation of teenagers who are preparing to go to Marsin this century.
The Mars Generation is playing at the Woods Hole Film Festival on Sunday at 5 pm. Sunita Williams will also be speaking on a panel about science and storytelling on Sunday at 2 pm.
Sunita Williams, American Astronaut and former Commander of the International Space Station. She tweets @Astro_Suni.
On her path to becoming an astronaut It was a little bit of a happenstance, and a lot of good luck, and a lot of perseverance. I wanted to be a veterinarian, and go to school in Boston. It didn't quite work out that way, and I ended up joining the Navy as a suggestion of my big brother. It was really awesome, and I didn't realize it at the time, but provided a lot of leadership and followership teamwork opportunities. And it led me down the path to become a helicopter pilot and a test pilot. It was the shoe in the door to making me understand that, hey things are possible. And I got down to NASA at Johnson Space Center and realized that I could do the things those guys were doing, like anybody can when they have that opportunity and take it.
On her time as a commander on the International Space Station It was awesome. A huge responsibility. But just like in the movie The Martian, you take it one step at a time. You don't look at the big problem all together, because I think it's a little intimidating. So you just take it one day at a time, meet the people who are going to meet with you, for you, and who you're going to work for, and really try to do the best job that you can. That's all teamwork, and that's what space travel is about.
On what it's like to do a spacewalk It's a little scary at times, when it's just your visor between you and the outside, not-so-nice area of space where there's no air to breathe a vacuum that's really hot, and really cold. So that's scary. But you take it one step at a time. You have a lot of things to do when you're out on a space walk, and that sort of overwhelms your mind. You're like, "I've got to get this test done, and this test done." But you can't help every now and then stopping, and looking at where you are, and watching the world whiz by you and just going, "Whoah! But never mind just keep working, just keep working." It is an incredible view, an incredible place to work, and it's the culmination of a huge team of people making it work for the astronauts who are just out there doing their jobs.
On what her time in space has taught her about the challenges facing potential Mars astronauts You are away from home, and you do miss your family and your friends, and of course I missed my dog. But you have the ability to call home, and the ability to video conference on the weekends. We're close to Earth, and we only have about a half-second of delay when we're talking. But when you take that trip and are going to Mars, you're going to have a long delay. You're not going to be able to have those instant conversations. You're going to need to know how to fix things without calling home to ask how to do it. So there's going to be a lot of different challenges for that crew, and that crew needs to know that they'll be gone for a long time. I knew I would be gone for 6 months, and maybe a little bit more. [People going to Mars] need to go into this knowing that you might be gone for a year and a half or so. You're not going to be able to text to your friends and family like people are used to doing here. It's going to take a little while to get that communication back and forth.
On whether the golden age of manned missions to space through NASA has passed, with the advent of space trips through the private sector. This is all a partnership. There's been so much technology that has transpired over the last 20, 30 years, and it's time to move that into the spacecraft. Who can better do that than the technology gurus out there who have been working in some of these companies? We're really excited to see what their innovative ideas bring to the table when they create these spacecraft. They're going to solve the problem for us of low-earth orbit, which means going to the International Space Station and delivering people. And that frees up NASA to work on exploration. The thing that we all want to do is get out of low-earth orbit and go farther, so we can figure out that problem of how to go to Mars. So we have a lot on our plate, but we are working hand-in-hand with these companies, so we can leverage information and technology off each other. And my personal opinion, Suni Williams I think that when we really leave the planet we all go as humans, not as people from one country or another. We are humans, we work together. This is our only planet as human beings that we know of. So we all should have an interest in preserving it.
On the idea of space tourism I think it's great. If these companies can go out there and lower the price for folks to go to space, that's going to enhance space travel and make it safer. We've gone through this kind of evolution with aircraft, and aircraft are pretty darn safe. We joke that one day, we'll have a space station on the moon, and the tourists up there will be going, "Where's my spacecraft to get me home? It's 10 minutes late!" Just like we do when we're standing in the airline line waiting to board our aircraft. I think it's a good thing. It's progress. It's evolution. We're going to make it all happen. And I think this next generation of kids in high school and younger we've got to set the stage for them, and they are going to make it happen.
On the most amazing thing she's ever witnessed in space There's so many things to say, but one things is the aurora. Watching the aurora from above is pretty spectacular. We live up here in the north, and sometimes we go to see our northern neighbors, where we can see the aurora at night, and see it above you and it's cool. But when you see it from above looking down below, and see that energy hitting the earth, it's spectacular. And you got to wonder there is a lot of energy out there in the universe that we have no idea how to capture and use. Our problems here on earth are a little slim compared to the real deal.
This segment aired on July 28, 2017.
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Astronaut Sunita Williams On Her Time In Space and 'The Mars Generation' - WBUR
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Adrin Villar Rojas Excavates Greece’s National Identity – Hyperallergic
Posted: at 6:48 pm
Installation view of Adrin Villar Rojas, The Theater of Disappearance (all images Panos Kokkinias, Courtesy NEON unless otherwise indicated)
ATHENS How do you define your national identity? Adrin Villar Rojass new installation/intervention, The Theater of Disappearance (2017) at the National Observatory of Athensseems to ask just that, prompting thoughts about what the soil beneath our feet contains and represents, and how far we should dive into the depths of our own past.
The Greeks have a very deep past to dive into, of course. To stand on this land is to stand within the cradle of Western civilization. History lives here in plain sight.The National Observatory is no exception; situated on the Hill of the Nymphs, it has an unrivaled view of the Acropolis. I am informed that it is difficult to build on or excavate this land, in case anything precious in the soil is disturbed. As the installations commissioner, NEON director Elina Kountouri, states in the exhibition catalogue, establishing the observatory in 1842 was fiercely opposed. It was argued that any digging would disrupt the tranquility and the architectural purity of the hill. Thus, Greek people lay their identity in earth that remains loaded with the debris of past events. Who should have authority to excavate it, I wonder: any of the archaeologists, politicians, or astronomers who have previously made their mark here, or an artist like the Argentinian-born Villar Rojas?
An additional subtext to The Theater of Disappearance is Greeces current national debt. Athens is a city that reveres its past, yet fears for its future. Meanwhile the other, concurrent large-scale art exhibition set in Athens, documenta 14, has been heavily criticized. Complaints leveled against Crapumenta include calling out the insensitivity of hosting an expensive festival in a place where residents are suffering financially, plus their initial underrepresentation of Greek artists. Villar Rojas is brave for questioning the foundations of national identity in the midst of this crisis.
Essentially, Villar Rojass Theater manifests itself in three ways: a large-scale landscaping of the observatory gardens, a complete re-staging of the observatorys interior, which is now a museum, and a transformation of wasteland at the back of the building into what can only be described as a dystopian, outdoor museum. Villar Rojas developed it over a four-month period, with the assistance of a large crew sourced locally and from his studio in Argentina.
Upon entry, I was surprised to encounter a lush vegetable garden. Athens is arid at this time of year; yet, plump, fleshy stalks of corn tower over beds of artichokes, pumpkins, and asparagus. The original gardens have disappeared, replaced by 46,000 edible plants. Yet he hasnt dug directly into the earth. Instead, a meticulously planned second level of soil sits on raised, irrigated beds. He spent at least two months clearing out dead trunks and leaves in preparation. Would the importance of this process of transforming a fiercely protected heritage site into a theater of food production be understood as acutely in any other city?
On the very top of the hill, the observatorys dome gleams in the sunlight. Inside, it is church-like: cool, very dark, and soundproofed by heavy grey curtains covering every wall and window. Again, some of the original archive has disappeared, edited down to a spare selection of objects placed carefully in each room one large telescope, a case of books, a clock. By peeping through a slim gap in the drapes, you can see the nearby Pantheon a Greek emblem and a grand backdrop that clearly indicates the locale. Villar Rojas is stage dressing. In the foyer, a plaster white, 3D-printed model of the observatory as it was in 1842 reminds visitors of the rocky hill it used to sit on before any landscaping an origin story, if you will. Villar Rojas is directing our attention to what he wants us to see, albeit things from the past that were already there, but now beheld in sharper focus.
Onwards, and Im instructed by an assistant to follow a winding path around the back of the building. The terrain suddenly becomes sandier and more precarious where am I heading? I start to see glass vitrines, embedded at impossible angles on a steep outcrop. Various objects are preserved behind the glass: the Curiosity Mars Rover, guns from the Falkland Islands war, medals from the Ottoman Turkish Empire, iPod wires, charred bones, tattered flags, a graffitied statue of what looks like the goddess Nike. The relics are placed on top of and within layers of pink and terracotta archaeological stratification, as if just unearthed. The work manages to be culturally sensitive and incendiary at the same time, bringing together familiar echoes from the past like mythology and rather more grubby ones that wed rather forget the Falklands, for example, which saw 649 Argentinian soldiers and 255 British soldiers die over just 74 days in the early 1980s.
The overall effect of The Theater of Disappearance the changed gardens, bare museum and somber vitrines is initially bewildering. Yet the longer you spend on this hill, the more that Villar Rojass piece prompts you to consider history, autonomy, and identity. Yes, this is already a site of historical importance, but the artist has directed our focus to questions about what is chosen to be preserved, and why the references made to the Space Race, recent armed conflict, defunct technology, and dead soldiers imply mans aggression, and how selective we can be in deciding which histories to cherish.
For example, one vitrine contains a deflated replica of Neil Armstrongs space suit, Ottoman military emblems, and a layer of moon dust: theres a footprint in the dust, and one plastic bag of seeds signifying mans colonization of the moon. Colonization is embedded in the Greeks development they founded outposts from Italy to North Africa, and were themselves under Turkish rule for 400 years. Theirs is a saga of magnificent achievement, and also of failure and death. The Greeks, says Villar Rojas in a public talk later that evening, have a dual history of being colonists and refugees. He paraphrases an anthropologist: When we dig, we find the enemy. When we dig, we also decide what ancestral experiences are significant to our personal and national identity important enough to conserve. My impression of Greeces history, from this exhibition, is one that is as complicated and contentious as my own British one. There are things that lie within my countrys soil cultural artifacts, gold, bones, blood that symbolize both pride and shame. I can relate.
I also get the impression that The Theater of Disappearance is unresolved. It is one of four exhibitions sharing the same title, showing at The Metropolitan Museum of Art, New York (April 14October 29), Kunsthaus Bregenz, Vorarlberg, Austria (May 6August 27), and the Geffen Contemporary at MOCA, Los Angeles (October 22February 26, 2018). Seen together, these theaters might give more insight into Villar Rojass views on history, autonomy, and identity. In short, this artist hasnt finished digging yet.
Adrin Villar Rojas, The Theater of Disappearance continuesat the National Observatory of Athens, (Lofos Nymphon, Thissio, Athens) Greece until September 24.
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True Blue Chrysanthemum Flowers Produced with Genetic Engineering – Scientific American
Posted: at 6:48 pm
Roses are red, but science could someday turn them blue. Thats one of the possible future applications of a technique researchers have used to genetically engineer blue chrysanthemums for the first time.
Chyrsanthemums come in an array of colours, including pink, yellow and red. But all it took to engineer the truly blue hueand not a violet or bluish colourwas tinkering with two genes, scientists report in a study published on July 26 inScience Advances. The team says that the approach could be applied to other commercially important flowers, including carnations and lilies.
Consumers love novelty, says Nick Albert, a plant biologist at the New Zealand Institute for Plant & Food Research in Palmerston North, New Zealand. And people actively seek out plants with blue flowers to fill their gardens.
Plenty of flowers are bluish, but its rare to find true blue in nature, says Naonobu Noda, a plant researcher at the National Agriculture and Food Research Organization near Tsukuba, Japan, and lead study author. Scientists, including Noda, have tried to artificially produce blue blooms for years:efforts that have often produced violet or bluish huesin flowers such as roses and carnations. Part of the problem is that naturally blue blossoming plants arent closely related enough to commercially important flowers for traditional methodsincluding selective breedingto work.
Most truly blue blossoms overexpress genes that trigger the production of pigments called delphinidin-based anthocyanins. The trick to getting blue flowers in species that arent naturally that colour is inserting the right combination of genes into their genomes. Noda came close in a 2013 studywhen he and his colleagues found that adding a gene from a naturally blue Canterbury bells flower (Campanula medium) into the DNA of chrysanthemums (Chrysanthemum morifolium) produced a violet-hued bloom.
Noda says he and his team expected that they would need to manipulate many more genes to get the blue chrysanthemum they produced in their latest study. But to their surprise, adding only one more borrowed gene from the naturally blue butterfly pea plant (Clitoria ternatea) was enough.
Anthocyanins can turn petals red, violet or blue, depending on the pigments structure. Noda and his colleagues found that genes from the Canterbury bells and butterfly pea altered the molecular structure of the anthocyanin in the chrysanthemum. When the modified pigments interacted with compounds called flavone glucosides, the resulting chrysanthemum flowers were blue. The team tested the wavelengths given off by their blossoms in several ways to ensure that the flowers were truly blue.
The quest for blue blooms wouldn't only be applicable to the commercial flower market. Studying how these pigments work could also lead to the sustainable manufacture of artificial pigments, says Silvia Vignolini, a physicist at the University of Cambridge, UK, who has studied themolecular structure of the intensely blue marble berry.
Regardless, producing truly blue flowers is a great achievement and demonstrates that the underlying chemistry required to achieve 'blue' is complex and remains to be fully understood, says Albert.
This article is reproduced with permission and wasfirst publishedon July 26, 2017.
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True Blue Chrysanthemum Flowers Produced with Genetic Engineering - Scientific American
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When genetic engineering is the environmentally friendly choice – eco-business.com
Posted: at 6:48 pm
Papaya trees bask in the evening light on a Hawaiian farm. Enabling crops to resist diseases through genetic modification was a key reason for the survival of Hawaii's papaya industry. Image: Eugene Kim, CC BY 2.0
Which is more disruptive to a plant: genetic engineering (GE) or conventional breeding?
It often surprises people to learn that GEcommonly causes less disruption to plantsthan conventional techniques of breeding. But equally profound is the realisation that the latest GE techniques, coupled with a rapidly expanding ability to analyse massive amounts of genetic material, allow us to make super-modest changes in crop plant genes that will enable farmers to produce more food with fewer adverse environmental impacts. Such super-modest changes are possible with CRISPR-based genome editing, a powerful set of new genetic tools that isleading a revolution in biology.
My interest in GE crops stems from my desire to provide more effective and sustainable plant disease control for farmers worldwide. Diseases often destroy 10 to 15 per cent of potential crop production, resulting inglobal losses of billions of dollars annually.
The risk of disease-related losses provides an incentive to farmers to use disease-control products such as pesticides. One of my strongest areas of expertise is in the use of pesticides for disease control. Pesticides certainly can be useful in farming systems worldwide, but they have significant downsides from a sustainability perspective. Used improperly, they can contaminate foods. They can pose a risk to farm workers. And they must be manufactured, shipped and applied all processes with a measurable environmental footprint. Therefore, I am always seeking to reduce pesticide use by offering farmers more sustainable approaches to disease management.
What follows are examples of how minimal GE changes can be applied to make farming more environmentally friendly by protecting crops from disease. They represent just a small sampling of thebroad landscape of opportunitiesfor enhancing food security and agricultural sustainability that innovations in molecular biology offer today.
Genetically altering crops the way these examples demonstrate creates no cause for concern for plants or people. Mutations occur naturally every time a plant makes a seed; in fact, they are the very foundation of evolution. All of the food we eat has all kinds of mutations, and eating plants with mutations does not cause mutations in us.
A striking example of how a tiny genetic change can make a big difference to plant health is the strategy of knocking out a plant gene that microorganisms can benefit from. Invading microorganisms sometimes hijack certain plant molecules to help themselves infect the plant. A gene that produces such a plant molecule is known as asusceptibility gene.
We can useCRISPR-based genome editingtocreate a targeted mutationin a susceptibility gene. A change of as little as a single nucleotide in the plants genetic material the smallest genetic change possible canconfer disease resistancein a way that is absolutely indistinguishable from natural mutations that can happen spontaneously. Yet if the target gene and mutation site are carefully selected, a one-nucleotide mutation may be enough to achieve an important outcome.
There is a substantial body of research showing proof-of-concept that a knockout of a susceptibility gene can increase resistance in plants to a very wide variety of disease-causing microorganisms. An example that caught my attention pertained topowdery mildew of wheat, because fungicides (pesticides that control fungi) are commonly used against this disease. While this particular genetic knockout is not yet commercialised, I personally would rather eat wheat products from varieties that control disease through genetics than from crops treated with fungicides.
The power of viral snippets
Plant viruses are often difficult to control in susceptible crop varieties. Conventional breeding can help make plants resistant to viruses, but sometimes it is not successful.
Early approaches to engineering virus resistance in plants involved inserting a gene from the virus into the plants genetic material. For example, plant-infecting viruses are surrounded by a protective layer of protein, called the coat protein. The gene for the coat protein of a virus calledpapaya ring spot viruswas inserted into papaya. Through a process called RNAi, this empowers the plant to inactivate the virus when it invades. GE papaya has been a spectacular success, in large partsaving the Hawaiian papaya industry.
Through time, researchers discovered thateven just a very small fragmentfrom one viral gene can stimulate RNAi-based resistance if precisely placed within a specific location in the plants DNA. Even better, they found we canstack resistance genesengineered with extremely modest changes in order to create a plant highly resistant to multiple viruses. This is important because, in the field, crops are often exposed to infection by several viruses.
Does eating this tiny bit of a viral gene sequence concern me? Absolutely not, for many reasons, including:
Tweaking sentry molecules
Microorganisms can often overcome plants biochemical defenses by producing molecules calledeffectorsthat interfere with those defenses. Plants respond by evolving proteins to recognise and disable these effector molecules. These recognition proteins are called R proteins (R standing for resistance). Their job is to recognise the invading effector molecule and trigger additional defenses.
A third interesting approach, then, to help plants resist an invading microorganism is to engineer an R protein so that it recognises effector molecules other than the one it evolved to detect. We can then use CRISPR to supply a plant with the very small amount of DNA needed to empower it to make this protein.
The latest GE techniques, coupled with a rapidly expanding ability to analyse massive amounts of genetic material, allow us to make super-modest changes in crop plant genes that will enable farmers to produce more food with fewer adverse environmental impacts.
This approach, like susceptibility knockouts, is quite feasible, based onpublished research. Commercial implementation will require some willing private- or public-sector entity to do the development work and to face the very substantial and costly challenges of the regulatory process.
The three examples here show that extremely modest engineered changes in plant genetics can result in very important benefits. All three examples involve engineered changes that trigger the natural defenses of the plant. No novel defense mechanisms were introduced in these research projects, a fact that may appeal to some consumers. The wise use of the advanced GE methods illustrated here, as well as others described elsewhere, has the potential to increase the sustainability of our food production systems, particularly given thewell-established safetyof GE crops and their productsfor consumption.
Paul Vincelli is Provosts Distinguished Service Professor at the University of Kentucky. This article is republished from Ensia.
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When genetic engineering is the environmentally friendly choice - eco-business.com
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Should genetic engineering be used as a tool for conservation? – chinadialogue
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Illustration by Luisa Rivere/Yale E360
The worldwide effort to return islands to their original wildlife, by eradicating rats, pigs, and other invasive species, has been one of the great environmental success stories of our time.Rewilding has succeeded on hundreds of islands, with beleaguered species surging back from imminent extinction, and dwindling bird colonies suddenly blossoming across old nesting grounds.
But these restoration campaigns are often massively expensive and emotionally fraught, with conservationists fearful of accidentally poisoning native wildlife, and animal rights activists having at times fiercely opposed the whole idea. So what if it were possible to rid islands of invasive species without killing a single animal? And at a fraction of the cost of current methods?
Thats the tantalising but also worrisome promise of synthetic biology, aBrave New Worldsort of technology that applies engineering principles to species and to biological systems. Its genetic engineering, but made easier and more precise by the new gene editing technology called CRISPR, which ecologists could use to splice in a DNA sequence designed to handicap an invasive species, or to help a native species adapt to a changing climate. Gene drive, another new tool, could then spread an introduced trait through a population far more rapidly than conventional Mendelian genetics would predict.
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Synthetic biology, also called synbio, is already a multi-billion dollar market, for manufacturing processes in pharmaceuticals, chemicals, biofuels, and agriculture. But many conservationists consider the prospect of using synbio methods as a tool for protecting the natural world deeply alarming. Jane Goodall, David Suzuki, and others havesigned a letterwarning that use of gene drives gives technicians the ability to intervene in evolution, to engineer the fate of an entire species, to dramatically modify ecosystems, and to unleash large-scale environmental changes, in ways never thought possible before.The signers of the letter argue that such a powerful and potentially dangerous technology should not be promoted as a conservation tool.
Environmentalists and synthetic biology engineers need to overcome what now amounts to mutual ignorance, a conservationist says.
On the other hand, a team of conservationbiologists writing early this yearin the journalTrends in Ecology and Evolutionran off a list of promising applications for synbio in the natural world, in addition to island rewilding:
Transplanting genes for resistance to white nose syndrome into bats, and for chytrid fungus into frogs and other amphibians.
Giving corals that are vulnerable to bleaching carefully selected genes from nearby corals that are more tolerant of heat and acidity.
Using artificial microbiomes to restore soils damaged by mining or pollution.
Eliminating populations of feral cats and dogs without euthanasia or surgical neutering, by producing generations that are genetically programmed to be sterile, or skewed to be overwhelmingly male.
And eradicating mosquitoes without pesticides, particularly in Hawaii, where they are highly destructive newcomers.
Kent Redford, a conservation consultant and co-author of that article, argues that conservationists and synbio engineers alike need to overcome what now amounts to mutual ignorance. Conservationists tend to have limited and often outdated knowledge of genetics and molecular biology, he says.Ina 2014 articleinOryx, he quoted one conservationist flatly declaring, Those were the courses we flunked. Stanford Universitys Drew Endy, one of the founders of synbio, volunteers in turn that 18 months ago he had never heard of the IUCN the International Union for Conservation of Nature or its Red List of endangered species.In engineering school, the ignorance gap is terrific, he adds.But its symmetric ignorance.
At a major synbio conference he organised last month in Singapore, Endy invited Redford and eight other conservationists to lead a session on biodiversity, with the aim, he says, of getting engineers building the bioeconomy to think about the natural world ahead of time My hope is that people are no longer merely nave in terms of their industrial disposition.
Likewise, Redford and the co-authors of the article inTrends in Ecology and Evolution, assert that it would be a disservice to the goal of protecting biodiversity if conservationists do not participate in applying the best science and thinkers to these issues. They argue that it is necessary to adapt the culture of conservation biologists to a rapidly-changing reality including the effects of climate change and emerging diseases.Twenty-first century conservation philosophy, the co-authors conclude, should embrace concepts of synthetic biology, and both seek and guide appropriate synthetic solutions to aid biodiversity.
Through gene drive technology, mice, rats or other invasive species can theoretically be eliminated from an island without killing anything.
The debate over synthetic biodiversity conservation, as theTrends in Ecology and Evolutionauthors term it, had its origins in a2003 paperby Austin Burt, an evolutionary geneticist at Imperial College London.He proposed a dramatically new tool for genetic engineering, based on certain naturally occurring selfish genetic elements, which manage to propagate themselves in as much as 99 percent of the next generation, rather than the usual 50 percent. Burt thought that it might be possible to use these super-Mendelian genes as a Trojan horse, to rapidly distribute altered DNA, and thus to genetically engineer natural populations. It was impractical at the time.Butdevelopmentof CRISPR technology soon brought the idea close to reality, and researchers have since demonstrated the effectiveness of gene drive, as the technique became known, in laboratory experiments on malaria mosquitoes, fruit flies, yeast, and human embryos.
Burt proposed one particularly ominous-sounding application for this new technology: It might be possible under certain conditions, he thought, that a genetic load sufficient to eradicate a population can be imposed in fewer than 20 generations. And this is, in fact, likely to be the first practical application of synthetic biodiversity conservation in the field. Eradicating invasive populationsis of coursethe inevitable first step in island rewilding projects.
The proposed eradication technique is to use the gene drive to deliver DNA that determines the gender of offspring.Because the gene drive propagates itself so thoroughly through subsequent generations, it can quickly cause a population to become almost all male and soon collapse.The result, at least in theory, is the elimination of mice, rats, or other invasive species from an island without anyone having killed anything.
Research to test the practicality of the method including moral, ethical, and legal considerations is already under way through a research consortium ofnonprofitgroups, universities, and government agencies in Australia, New Zealand, and the United States.At North Carolina State University, for instance, researchers have begun working with a laboratory population of invasive mice taken from a coastal island.They need to determine how well a wild population will accept mice that have been altered in the laboratory.
The success of this idea depends heavily,according togene drive researcher Megan Serr, on the genetically modified male mice being studs with the island lady mice Will she want a hybrid male that is part wild, part lab? Beyond that, the research programme needs to figure out how many modified mice to introduce to eradicate an invasive population in a habitat of a particular size. Other significant practical challenges will also undoubtedly arise.For instance,a study early this yearin the journalGeneticsconcluded that resistance to CRISPR-modified gene drives should evolve almost inevitably in most natural populations.
Political and environmental resistance is also likely to develop.In an email, MIT evolutionary biologist Kevin Esvelt asserted that CRISPR-based gene drives are not suited for conservation due to the very high risk of spreading beyond the target species orenvironment. Even a gene drive systemintroduced toquickly eradicate an introduced population from an island, he added, still is likely to have over a year to escape or be deliberately transported off-island. If it is capable of spreading elsewhere, that is a major problem.
Even a highly contained field trial on a remote island is probably a decade or so away, said Heath Packard, of Island Conservation, a nonprofit that has been involved in numerous island rewilding projects and is now part of the research consortium.We are committed to a precautionary step-wise approach, with plenty of off-ramps, if it turns out to be too risky or not ethical.But his group notes that 80% of known extinctions over the past 500 or so years have occurred on islands, whicharealso home to 40% of species now considered at risk of extinction. That makes it important at least to begin to study the potential of synthetic biodiversity conservation.
Even if conservationists ultimately balk at these new technologies, business interests are already bringing synbio into the field for commercial purposes.For instance, a Pennsylvania State University researcher recently figured out how to use CRISPR gene editing to turn off genes that cause supermarket mushrooms to turn brown.The USDepartment of Agriculturelast year ruledthat these mushrooms would not be subject to regulation as a genetically modified organism because they contain no genes introduced from other species.
With those kinds of changes taking place all around them, conservationists absolutely must engage with the synthetic biology community, says Redford, and if we dont do so it will be at our peril. Synbio, he says, presents conservationists with a huge range of questions that no one is paying attention to yet.
This article originally appeared on Yale Environment 360 and is republished here with permission.
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Scientists Give a Chrysanthemum the Blues – New York Times
Posted: at 6:48 pm
Plant species blooming blue flowers are relatively rare, Naonobu Noda, a plant biologist at the National Agriculture and Food Research Organization in Japan who led the research, noted in an email.
It took Dr. Noda and his colleagues years to create their blue chrysanthemum. They got close in 2013, engineering a bluer-colored one by splicing in a gene from Canterbury bells, which naturally make blue flowers. The resulting blooms were violet. This time, they added a gene from another naturally blue flower called the butterfly pea.
Both of these plants produce pigments for orange, red and purple called delphinidin-based anthocyanins. (Theyre present in cranberries, grapes and pomegranates, too.) Under a few different conditions, these pigments, which are sensitive to changes in pH, can start a chemical transformation within a flower, rendering it blue.
The additional gene did the trick. It added a sugar molecule to the pigment, shifting the plants pH and altering the chrysanthemums color. The researchers confirmed the color as blue by testing its wavelengths in the lab.
What they did was already being done in nature: No blue flowers actually have blue pigment. Neither do blue eyes or blue birds. They all get help from a few clever design hacks.
Blue flowers tend to result from the modification of red pigments shifting their acidity levels, switching up their molecules and ions, or mixing them with other molecules and ions.
Some petunias, for example, have a genetic mutation that breaks pumps inside their cells, altering their pH and turning them blue. Some morning glories shift from blue upon opening to pink upon closing, as acidity levels in the plant fluctuate. Many hydrangeas turn blue if the soil is acidified, as many gardeners know.
In vertebrates, blue coloring often is more about structure. Blue eyes exist because, lacking pigments to absorb color, they reflect blue light. Blue feathers, like those of the kingfisher, would be brown or gray without a special structural coating that reflects blue.
Reflection is also the reason for the most intense color in the world, the shiny blue of the marble-esque Pollia fruit in Africa.
Despite widespread blue-philia, the new chrysanthemums may meet a cool reception. A permit is required to sell genetically modified organisms in the United States, and there isnt one for these transgenic flowers.
Officials are wary of transgenic plants that might take root in the environment, because of their possible impacts on other plants and insects. Dr. Noda and his colleagues are working on blue chrysanthemums that cant reproduce, but its unlikely youll see them in the flower shop anytime soon.
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US Scientists Just Edited a Human Embryo for the First Time. (Yes, People Are Freaking Out.) – Mother Jones
Posted: at 6:47 pm
Heres what you need to know.
Kate HarloeJul. 28, 2017 1:35 PM
Ben Birchall/Associated Press
For the first known time in the United States, scientists used a gene-editing technique called CRISPR to modify early-stage human embryos, according to a report published Wednesday in MIT Technology Review.
Since the development several years ago ofCRISPR, a tool that allows scientists to change sequences of DNA within a cell, scientists have speculated about its potential to free families of genetic disease or stop the spread of other diseases like malaria, among other possibilities. But the technology also raises major ethical questions.
Heres a quick rundown of the latest breakthroughand how it could change the way we think about humanreproduction and, well, humans themselves.
How did the experiment work?
According to MIT Technology Reviews report, a team of researchers at Oregon Health & Science University, led by geneticist Shoukhrat Mitalipov, used CRISPR to correct disease-causing genes in human embryos. Its not yet clear whether these were viable embryosembryos that could, theoretically, grow into humans.
A wide range of diseaseslike Huntingtons, sickle-cell anemia, and Tay-Sachs, for exampleare caused by mutations in genes. Its also not clear what genes Mitalipov and his team edited in their experiment. But regardless, it appears that their study was successful in a couple ways: First, they reportedly edited a greater number of embryos than scientists had in previous studies. Second, Mitalipov and his team claim they did so without causing as manyerrors as previous scientists.
CRISPR has been used to edit human embryos a few times before; Chinese scientists did it in March. But in prior experiments, scientists ran into problems when CRISPR edits were taken up only by some of the cells in an embryo. This is called mosaicism:it means that the child that develops from the embryo could still inherit the disease that scientists tried to edit away.
According to MITs report, Mitalipov reduced the occurrence of mosaicism and seemed to largely avoid off-target edits (another kind of CRISPR error, wherein scientists accidentally alter a gene other than the one they aim to change).
Why is this important?
A couple reasons. First, its the only known attempt to use CRISPR to edit human embryos in the United States. More on the legality of that below.
Second, if this attempt really was successful, its big news for people whose families carry genetic disease. In theory, using this technique, scientists could edit not just our offspring, but our offsprings offspring. This is called human germline editing. When scientists edit the DNA in an embryo, the changes will theoretically be inherited by each successive generation, permanently fixing the germlinethe genetic inheritanceof a family.
This seems ethically complex.
Right. The ethics and laws surrounding human germline editingare murky. Scientists in favor of human germlinemodification often argue that the techniquewill help us reduce the occurrence of genetic diseases.
But criticsdisagree.This is just not needed for preventing inheritable disease, said Marcy Darnovsky, Executive Director of the Center for Genetics and Society. There are [other techniques that] can already be used safely to prevent the births of children with serious genetic diseases in almost every case. One example of such a technique is preimplantation diagnosis, commonly referred to as PGD, which allows parents to screen embryos for certain disease-causing genes before implanting them through in vitro fertilization (IVF). But its not always effectiveif someone carries two copies of a defective gene, for example, all their embryos would carry that gene, as well.
Darnovsky also worries about safety. Despite whatever the claims are about safety, [like] no mosaicism, we still dont know if that would mean its safe to create a new human being and anyone who tried it would be taking an enormous and unacceptable risk with that future persons life.
Another concern: Right now, scientists aresupposed to stick to editing disease-causing genes. But the technology opens up the possibility of editing genes for enhancementallowing parents to edit for certain kinds of physical and behavioral characteristics in their children. Darnovsky worries that this would usher in an era of genetic discrimination. That would be layering new forms of inequality and discrimination onto the ones we already live with, she said.
Is this legal?
Probably.In 2015, Congress passed a law forbidding the Food and Drug Administration from reviewing applications for germline editing of human embryos, meaning no clinical trials can move forward with FDA funding. We dont yet knowhow Mitalipov funded his project, but assuming it was funded privately, its perfectly legal.
That wouldnt be the case in many other countries. The Center for Genetics and Society reports that over 40 countries, including most with established biotech sectors, have established legal prohibitions on germline modification for human reproduction. An international treaty also prohibits it. The United States has no such policy.
Whats next?
Well know more once the study is released, but its worth noting that in February of this year, the National Academy of Sciences and the National Academy published a report that said human germline editing could be permitted in the future. It outlined criteria for germline editing, recommending that it only be used for disease prevention. The authors of the report wrote that editing for the enhancement of human traits and capacities should not be allowed at this time. But the report didnt eliminate the possibility of editing for enhancement in the future.
Reactions to the report were mixed. Some experts, like Darnovsky, feel that human germline modification should not be done for any purpose. But in an interview with Science, Eric Lander, president and founding director of MIT and Harvards Broad Institute, a genomics research center, said he thought the report struck the right balance of optimism and caution. They want to put friction tape on the slope so the slope isnt slippery, Lander said. Whether and for how long the tape will hold is an open question.
Mother Jones is a nonprofit, and stories like this are made possible by readers like you. Donate or subscribe to help fund independent journalism.
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US Scientists Just Edited a Human Embryo for the First Time. (Yes, People Are Freaking Out.) - Mother Jones
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Scientists Crispr the First Human Embryos in the US (Maybe) – WIRED
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As powerful as the gene-editing technique Crispr is turning out to beresearchers are using it to make malaria-proof mosquitoes , disease-resistant tomatoes, live bacteria thumb drives , and all kinds of other crazy stuffso far US scientists have had one bright line: no heritable modifications of human beings.
On Wednesday, the bright line got dimmer. MIT Technology Review reported that, for the first time in the US, a scientist had used Crispr on human embryos.
Behind this milestone is reproductive biologist Shoukhrat Mitalipov, the same guy who first cloned embryonic stem cells in humans. And came up with three-parent in-vitro fertilization . And moved his research on replacing defective mitochondria in human eggs to China when the NIH declined to fund his work. Throughout his career, Mitalipov has gleefully played the role of mad scientist, courting controversy all along the way.
Yesterdays news was no different. Editing viable human embryos is, if not exactly a no-no, at least controversial. Mitalipov and his colleagues at Oregon Health and Science University fertilized dozens of donated human eggs with sperm known to carry inherited disease-related mutations, according to the Tech Review report. At the same time, they used Crispr to correct those mutations. The team allowed the embryos to develop for a few days, and according to the original and subsequent reports a battery of tests revealed that the resulting embryos took up the desired genetic changes in the majority of their cells with few errors. Mitalipov declined to comment, saying the results were pending publication next month in a prominent scientific journal.
Big if true, as the saying goes. Mitalipovs group never intended to implant the eggs into a womb, but the embryos were clinical quality and probably could have survived implantation. That makes this only the second time scientists anywhere have edited viable embryosif thats indeed what Mitalipov did. Maybe this news is important enough to make it to the popular press without a peer-reviewed, published paper, but without one its impossible to be definitive on what Mitalipov actually did versus what hes claiming to have done.
Lets say its all real. Is it creepy? Maybe. But its also legalat least in Oregon, where embryo research is kosher as long as it doesnt involve federal funding. Officials at OHSU confirmed that the work took place there, and that it met the universitys Institutional Review Board criteria for safeguarding the rights and welfare of subjects involved in human researchpresumably the donors of the eggs and sperm, in this case. No one on the outside knows which exact genetic tweaks the researchers actually made or how safe the procedure was. Tech Review was light on details.
That lack of transparency could turn into a real problem. These are special cells and they should have special considerations given to them if youre going to Crispr them, says Paul Knoepfler, a stem cell researcher at UC Davis who wrote a book on designer babies called GMO Sapiens . Knoepfler worries that incautious work like this could lead to political backlash against Crispr more broadly, like what happened to stem cell research in the 2000s under George W. Bush. We dont have an unlimited amount of time to talk about these things and figure them out, Knoepfler says. This stuff is moving at warp speed and we need to get our act together on establishing guidelines that are much clearer about what is OK and what isnt.
Not that scientists havent tried. In February the National Academy of Sciences produced a report with its first real guidelines for Crispr research. It did not go so far as to place a moratorium on gene editing of the human germlinemodifications that a persons offspring could inheritthough it did suggest limitations. Scientists are only supposed to edit embryos to prevent a baby from inheriting a serious genetic disease, and only if the doctors meet specific safety and ethical criteria, and if the parents have no other options.
Those obstacles arent insurmountable, and a particularly slippery slope winds between them. At the Aspen Ideas Festival last month, UC Berkeley biologist Jennifer Doudna , one of the people who discovered Crispr, stressed the need for a unified policy on germline editing before scientists really start doing it. Once that begins, I think it will be very hard to stop, she said. Itll be very hard to say, Ill do this thing but not that thing. And at that point, who decides?
In the US, itll probably be the federal government. Congress has already banned federal funding for the human testing of gene-editing techniques that could produce modified babies. That provision is tucked into an appropriations rider that has to be renewed each year, so its an annually moving target. Congress has also barred the US Food and Drug Administration from even considering clinical trials of embryo editing. But even if those laws did change, the FDAs approval process for these kinds of technologies is among the strictest in the world. They would require years and years of animal studies before the first test embryo could conceivably be conceived.
Sarah Zhang
Crispr Is Getting Better. Now It's Time to Ask the Hard Ethical Questions
Nick Stockton
Read This Before You Freak Out Over Gene-Edited Superbabies
Nic Cavell
The UK Just Green-Lit Crispr Gene Editing in Human Embryos
For this to be something other than just a reckless person doing something crazy, were looking at least a decade and maybe more of safety testing, says Hank Greely, a law professor and bioethicist at Stanford. In countries with laxer laws, it could happen soonerlike, say, China , where scientists have reported three attempts at using Crispr to modify human embryos.
The first two studies used genetically defective embryos that could never come to term, but the most recent, published in March, used viable embryos. And while all three studies produced mixed results, Crispr was most successful at repairing faulty genes in the normal embryos. Experiments are also moving forward in Sweden and the UK that use Crispr to knock out different genes in viable embryos to study effects on development.
Still, dont panic . Modifying embryos that are never going to be implanted is not close to the boundary, Greely says. Doing it in embryos you might want to implant is real close to the boundary and shouldnt be done without any discussion. But thats not what Mitalipov did. Maybe. All the institutions apparently involved with the research refused to comment citing an embargo, which would make sense if there were an embargo to break. There wasn't, according to Antonio Regalado, who covers genetics for Tech Review but didn't write this story. Consider it instead just a good new-fashioned leak.
If you think of viable-embryo Crispr research as a journey and not a destination, right now scientists all over the world are on the same path. But at some point the road will fork: Someone will implant an engineered embryo into a human womb. The work coming out of China and Mitalipov's lab has this implied assumption that someday it will wind up being used heritably in humans, Knoepfler says. And I think that requires a unique obligation for being more open about it. Mitalipov's research is not a good start.
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