Engineering biodiversity as a model for the species conservation*

early humans have domesticated plant and animal species based on ancient empirical concepts (Darwin 1868, 1876). In 1886, Mendel established a new paradigm of hereditary laws (Mendel 1866, 1870, 1950) based on genotypic and phenotypic traits of cross-compatible species, establishing a complex breeding technology that is currently utilized for the development of most food and livestock-derived products. Recently, studies on deciphering the double-helical structure (Watson and Crick 1953a, b) and how to restrict DNA (Arber 2012) have established the foundation of recombinant DNA technology. A new era is paving the way for genetic manipulation of important traits among all the kingdom’s organisms, allowing for the development of innovative and widely utilized products for the agricultural, industrial and pharmaceutical production sectors (Mc elroy 2003, 2004, ISAAA 2016).


INTRODUCTION
Brazil has a significant percentage of the economic matrix generated in agribusiness and also constitutes a region of mega-biodiversity.Where conservation and sustainable use of biodiversity is the physical basis for agribusiness, exerted through water resources, water availability, genetic resources, soil conservation, climate stability, and nutrient recycling, among other physical factors and chemicals.
The Amazon region is home to a megabiodiversity (Soares et al. 2006).Different models have been proposed (Peres and Terborgh 1995, Schwartzman et al. 2000, Merry et al. 2003, Nepstad et al. 2002, 2006, Soares-Filho et al. 2006, gullison et al. 2007) with the aim of establishing an active conservation policy, sustainable use and added value for biodiversity.Over the years the Amazon region has been submitted to a vicious circle that involves devastation of the forest and falling employment.There is a hypothesis linking a reduction in deforestation and an increase in governance with the higher employment and income that is associated with development in various processes and products, and this has been extolled as a virtuous development circle (Nepstad et al. 2002).Besides, generating carbon credits has been suggested as a viable development strategy for the region (Nepstad et al. 2006b, Stern 2006).In contrast, it has been demonstrated that recent significant losses of forest and rising incomes can be linked mainly to the expansion of cattle-farming and soy-growing industries (Nepstad et al. 2006b It is accepted that the real value of biodiversity is still unknown and any estimates are speculative.The Amazon region is so complex that it needs studies based on added value as a factor that, in turn, depends on technological advances.Currently, a broad spectrum of technologies associated with recombinant DNA is available, and these permit the collection, manipulation and practical evaluation of many molecules that come from biodiversity. early humans have domesticated plant and animal species based on ancient empirical concepts (Darwin1868,1876).In 1886, Mendel established a new paradigm of hereditary laws (Mendel, 1866(Mendel, , 1870(Mendel, , 1950) ) based on genotypic and phenotypic traits of cross-compatible species, developing a sophisticated breeding technology utilized for the development of most food and livestock-derived products.Recently, studies on deciphering the double-helical structure (Watson and Crick 1953a, b) and how to restrict DNA (Arber 2012) have established the foundation of recombinant DNA technology.A new era is paving the way for genetic manipulation of important traits among all the kingdom's organisms, allowing for the development of innovative and widely utilized products for the agricultural, industrial and pharmaceutical production sectors (Mc elroy 2003, 2004, ISAAA 2016).
Currently, it is possible to state that the world has reached the mature stage of recombinant DNA technology, which, in turn, may allow us to envisage the capacity to generate a significant number of novel processes and products for the benefit of human beings and sustainable utilization and conservation of biodiversity and the environment as a whole.One possibility termed "synthetic domestication of useful traits" (Rech and Arber 2013).Although technical issues are still a challenge, the broad potential of progress is accelerating.Nevertheless, ethics and a comprehensive regulatory system ought to be discussed to guarantee deeper and higher standards of deregulation before any product reaches the market.
Currently, available tools and technologies for synthetic domestication of useful traits have opened the door for another breakthrough in scientific progress (Cermak et al. 2011, Doyon et al. 2011, gibson et al. 2008, Rech and Arber 2013, Cong et al. 2013, Boch et al. 2009, Carlson and lancto 2016).Making use of genome editing (Boch et al. 2009, Mali et al. 2013, li et al. 2013, Jiang et al. 2013, Cong et al. 2013, Doudna and Charpentier 2014, Carlson and lancto 2016), a template founded on molecular synthesis, assembly and synthetic biology (Yu et al. 2006, gibson et al. 2008, 2010, Annaluru et al. 2014, Hutchison et al. 2016), has allowed for the sustainable prospection and manipulation of innovative traits found in biodiversity.examples follows here which should fit within the concept of "synthetic domestication of useful traits", through the utilization of recombinant DNA technology and genetic engineering directing the sustainable use of biodiversity.

PRODUCTION OF SYNTHETIC SPIDER FIBRE
Spider silk fibre has been noted for its unique physical and mechanical properties and recognized as a protein-based nanomaterial (lewis 2006, Silva andRech 2013).To this end, the functional genome of different Brazilian spiders' silk glands have been studied, considering evolution and evaluating the potential development of novel biopolymers through synthetic biology (Bittencourt et al. 2010, Prosdocimi et al. 2011).Drawing on genome and transcriptome data, it has become possible to design de novo proteins and produce synthetic spider-like fibres in bacteria.Which, in turn, has led to the development of alternative strategies for the production of synthetic silk proteins using recombinant DNA technology (Teulé et al. 2009, Murad andRech 2011).A complete procedure for the artificial spinning of fibres made from recombinant proteins based on chimeric or native synthetic spider silk-like sequences was developed and produced through genetic engineering in E. coli.
The strategy is to build large synthetic spider silklike tandem repeat sequences from small doublestranded monomer DNAs flanked by compatible but non-regenerable restriction sites (Figure 1 and 2).

ENGINEERING SOYBEAN SEEDS AS A SCALABLE PLATFORM TO PRODUCE A MICROBICIDE AGAINST HIV
There is an urgent need to provide effective anti-HIV microbicides to resource-poor areas worldwide.Some of the most promising microbicide candidates are biotherapeutics targeting viral entry.
For availability of biotherapeutics to poorer areas, it is vital to reduce their cost.Cyanovirin-N (CV-N), an 11 009 Da protein isolated from cultures of the cyanobacterium Nostoc ellipsosporum, is a potent lectin capable of irreversibly inactivating diverse strains of HIV (types 1 and 2) and simian immunodeficiency virus (Boyd et al. 1997).
We report the production of biologically active recombinant cyanovirin-N (rCV-N), an antiviral protein, in genetically engineered soybean seeds.Pure, biologically active rCV-N was isolated with a yield of 350 µg/g of dry seed weight.rCV-N purified from soya is active in anti-HIV assays, with an eC50 of 0.82-2.7 nM (compared to 0.45-1.8nM for E. coli-produced CV-N).Standard industrial processing of soya bean seeds to harvest soya bean oil does not diminish the antiviral activity of recovered rCV-N, allowing the use of industrial soya bean processing to generate both soya bean oil and a recombinant protein for anti-HIV microbicide development (O'Keefe et al. 2015).expression of rCV-N was achieved using specific regulatory sequences within soybean seed tissues (Rech et al. 2008).One of the difficulties in fully evaluating CV-N as a microbicide has been the high cost of production.CV-N produced in soybean seeds addresses this critical requirement, and soya beans should be evaluated as a production system to produce other suitable candidate microbicides for further preclinical evaluation and, possibly, clinical testing in humans.Development of a suitable expression source for the manufacture of an anti-HIV topical microbicide requires a lowcost methodology to have the broadest utility in the areas of the world most affected by HIV (Essex  Suitable microbicide candidates must meet an array of criteria.Although potential microbicides meeting some of these functional criteria are available, few microbicides have been able to be produced at sufficiently low cost (Figure 3).

REGULATORY GENE CIRCUITS UTILIZING SERINE INTEGRASES
Although single genetic switches and circuits are in the early stage of development, it is possible to envisage a not-too-distant future in which multiple switches become the norm, allowing increasingly precise control of gene regulation and expression in plants and mammalian cells for the development of innovative processes and products for the benefit of human beings and the environment.Studies on gene regulation have demonstrated effective control of the RNA polymerase flux by utilizing different serine integrases, which are capable of catalysing unidirectional inversion of DNA to turn on/off regulatory genes in prokaryotic cells (Schwille 2011, Nandagopal and elowitz 2011, Bonnet et al. 2013, Yang et al. 2014, Nielsen et al. 2016, Weinberg et al. 2017).A simplified mathematical model was proposed to explain and define core features that are demanded and sufficient for the regulation of both 'forward' and 'reverse' integrase reactions (Pokhilko et al. 2017).In this model, the substrates of the 'forbidden' reactions (between attl and attR in the absence of RDF and between attP and attB in the presence of RDF) are trapped as inactive protein-DNA complexes, ensuring that these 'forbidden' reactions are prolonged.The model is in good agreement with the observed in vitro kinetics of recombination by φC31 integrase, and it defines the core features of the system that are necessary and sufficient for directionality.
However, knowledge about the functionality of integrases in eukaryotic cells is still limited.Here, we show the remarkable functional capability of bacteriophages' serine integrases acting in plant and mammalian cells.A co-transformation plasmid system was utilized for in vitro evaluation of different integrases in Arabidopsis thaliana protoplasts, bovine fibroblasts, and human cells.The first plasmid contained the codon-optimized integrase 2 gene and integrase 5 gene sequences under inducible promoters.The second plasmid was a reporter plasmid that contains the gfp gene under the 35SCaMV promoter placed in reverse complement orientation and flanked by the attB and attP sites of both integrases.Once the integrases were expressed, the promoter sequence was flipped to its correct orientation, promoting GFP (green fluorescent protein) expression.The results obtained demonstrated that the promoter was correctly flipped, which, in turn, led to RNA polymerase flux through the DNA molecule and gFP expression, as detected by fluorescence microscopy and flow cytometry.The promoter inversion was detected by PCR and sequencing analyses.We anticipate our results to be an initial point for development of more complex models of gene regulation in plants using synthetically engineered integrases.Currently, we have been utilizing recombinases, such as serine integrases, to determine the endogenous nonessential genes within genomes.This fact may allow to design and provide systems to control endogenous and exogenous gene regulation through the development of synthetic genetic circuits, which, through external chemical, physical and biological inducers, are capable of switching specific traits "on" and "off" in model eukaryotic organisms (Coelho et al. 2017; Figure 4).
In addition to the efforts made to conserve biodiversity, an effective increase in estimates of the value of biodiversity is needed, based on evidence.The use of biotechnology may constitute a valuable tool and viable option for the advocated evaluation of biodiversity as well as for its sustainable use and production of innovative molecules.Biotechnology aiming the synthetic domestication of useful traits may well fit as a virtuous circle option.Due to the urgency and strategic importance, the operational evaluation of biodiversity should be associated with the establishment of partnerships between the public and private sectors, along with necessary interactions with developed countries as a relevant foundation.

Figure 2 -
Figure 2 -A representative atomic force microscopy image of the topographic surface of a synthetic spider silk-like fibre made from the synthetic recombinant protein MaSp 2 from Parawixia bistriata.

Figure 3 -
Figure 3 -Concentration dependant anti-HIV activity of purified rCV-N on HIV-1 RF infected () and uninfected () CeM-SS cells assessed after 6 days in culture.The number of surviving cells was measured by the XTT method and is indicated as percent untreated uninfected cell control.Pure rCV-N (infected) had an eC 50 value of 20.82nM and an IC 50 of 284.55nM.The CC 50 was 280.71nM for the uninfected sample.The dotted line indicates untreated virus-infected cell controls and the dashed line indicates untreated, uninfected cell controls.error bars indicate standard deviation of the mean values obtained from triplicate samples (O'Keefe et al. 2015).

Figure 4 -
Figure 4 -Diagram of in silico design of a genetic circuit.Representation of the two plasmid system used to evaluate the functionality of the integrases in plant cells.Integrase plasmids containing two different Arabidopsis thaliana codon-optimized integrases under inducible promoters and the reporter plasmid containing egFP under a CaMV 35S promoter at the reverse orientation and flanked by the recognition sites of the integrases, before induction and at forwarding orientation after induction (Coelho et al. 2017). ).