<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">AiM</journal-id><journal-title-group><journal-title>Advances in Microbiology</journal-title></journal-title-group><issn pub-type="epub">2165-3402</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/aim.2020.108029</article-id><article-id pub-id-type="publisher-id">AiM-102537</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject></subj-group></article-categories><title-group><article-title>
 
 
  Biotechnological Potential of Carotenoids Produced by Extremophilic Microorganisms and Application Prospects for the Cosmetics Industry
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Tayane</surname><given-names>de Cássia Dias Mendes-Silva</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Rosileide</surname><given-names>Fontenele da Silva Andrade</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Marcio</surname><given-names>Akio Ootani</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Paulo</surname><given-names>Vitor Dias Mendes</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Rafael</surname><given-names>Artur de Queiroz Cavalcanti de Sá</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Milena</surname><given-names>Roberta Freire da Silva</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Karolayne</surname><given-names>Silva Souza</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Maria</surname><given-names>Tereza dos Santos Correia</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Márcia</surname><given-names>Vanusa da Silva</given-names></name><xref ref-type="aff" rid="aff5"><sup>5</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Maria</surname><given-names>Betânia Melo de Oliveira</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Biochemistry, Federal University of Pernambuco, Recife, Brazil</addr-line></aff><aff id="aff5"><addr-line>Nucleus of Bioprospecting and Conservation of the Caatinga, Semiarid National Institute/Ministry of Science, Technology, 
Innovations and Communications, Campina Grande, Brazil</addr-line></aff><aff id="aff4"><addr-line>Design Department, Federal University of Pernambuco, Recife, Brazil</addr-line></aff><aff id="aff2"><addr-line>National Program Postdoctoral CAPES (PNPD), Catholic University of Pernambuco, Recife, Brazil</addr-line></aff><aff id="aff3"><addr-line>Bioprocess Laboratory, Center of Strategic Technologies Northeast, Recife, Brazil</addr-line></aff><pub-date pub-type="epub"><day>13</day><month>08</month><year>2020</year></pub-date><volume>10</volume><issue>08</issue><fpage>397</fpage><lpage>410</lpage><history><date date-type="received"><day>22,</day>	<month>July</month>	<year>2020</year></date><date date-type="rev-recd"><day>25,</day>	<month>August</month>	<year>2020</year>	</date><date date-type="accepted"><day>28,</day>	<month>August</month>	<year>2020</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
   
    Carotenoids are isoprenoid pigments used in food, chemical, textile, pharmaceutical, and cosmetic industries. They act not only as dyes and provitamins A but also have antioxidants, photoprotective, antimicrobial properties, among others. This class of pigment can be obtained traditionally by plants or chemical synthesis, but they have some disadvantages. In recent years, search for alternative sources has been an important strategy for the carotenoid industries. Microbial synthesis is an alternative that has shown good yields, speed, and reduced production costs. Hostile environments, such as the Caatinga domain, represent an interesting source of microorganisms that produce biomolecules, especially carotenoids, because of oxidative stress caused by sunlight. Thus, this region has been attracting the attention of the scientific community and industry for the use of these organisms in the production of carotenoids and applications in cosmetic products; since these compounds have interesting antioxidant and photoprotective properties. In this review, general characteristics of carotenoids, sources of production, industrial applicability, and commercialization will be discussed, as well as perspectives on the production of carotenoids from microorganisms isolated from the Caatinga and their application in anti-UV products.    
    
   
  
 
</p></abstract><kwd-group><kwd>Natural Pigment</kwd><kwd> Microbial Production</kwd><kwd> Hostile Environments</kwd><kwd> Antioxidant</kwd><kwd> Photoprotection</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>The word carotenoid is derived from the scientific name of the carrot Daucus carote, identified by Wackenroder in 1831 as the first source of carotene [<xref ref-type="bibr" rid="scirp.102537-ref1">1</xref>]. Carotenoids are one of the classes of natural pigments often found in fruits and vegetables. Also, they are produced by algae, filamentous fungi, yeasts, and bacteria [<xref ref-type="bibr" rid="scirp.102537-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref3">3</xref>]. These pigments are responsible for the colors bright yellow, orange, and red [<xref ref-type="bibr" rid="scirp.102537-ref4">4</xref>].</p><p>Most of the commercialized carotenoids are from vegetable extraction and chemical synthesis. Some problems in the production and commercialization of these dyes, such as seasonal and geographical variability, cannot be controlled [<xref ref-type="bibr" rid="scirp.102537-ref5">5</xref>]. On the other hand, chemical synthesis is a generally complex process that causes the formation of hazardous and inappropriate waste when disposed of in the environment; also, this is not considered safe for health [<xref ref-type="bibr" rid="scirp.102537-ref6">6</xref>]. This results in general concern, which reverberates in many discussions about the unwanted effects of these artificial pigments and the future impacts on human health [<xref ref-type="bibr" rid="scirp.102537-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref8">8</xref>].</p><p>Therefore, the synthesis of carotenoids by microorganisms is a viable strategy, which meets the safety marketing appeal and makes it possible to obtain these natural pigments on an industrial scale, quickly and efficiently [<xref ref-type="bibr" rid="scirp.102537-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref10">10</xref>]. Unlike traditional production, the microbial pathway for the production of carotenoids does not depend on external factors and on the seasonal supply of raw materials, which allows the generation of vast pigment yields with diverse coloring [<xref ref-type="bibr" rid="scirp.102537-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref10">10</xref>].</p><p>Some microorganisms, known as extremophiles, grow in hostile or extreme environments [<xref ref-type="bibr" rid="scirp.102537-ref11">11</xref>]. They are described as potential producers of natural molecules of biotechnological interest. The Caatinga Domain is a very particular habitat with high temperatures, in which the soil can reach 60˚C in periods of drought, thus characterized as an environment of adverse conditions for the growth of microorganisms [<xref ref-type="bibr" rid="scirp.102537-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref14">14</xref>].</p><p>Some microorganisms can accumulate carotenoids in response to environmental stress, such as oxidative stress caused by high solar incidence, which contributes to their survival and competitiveness. Although these microorganisms and their ability to synthesize pigments are poorly investigated [<xref ref-type="bibr" rid="scirp.102537-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref16">16</xref>], bioprospection of unknown microorganisms, as a source of new carotenoids, has been highlighted as a focus of research in the biotechnological area [<xref ref-type="bibr" rid="scirp.102537-ref17">17</xref>].</p><p>The carotenoids extracted from these organisms stimulate applications in cosmetic products, as they have antioxidant properties, solubility and stability in oil-in-water emulsions, which are attractive for application in sunscreens and other anti-UV products [<xref ref-type="bibr" rid="scirp.102537-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref19">19</xref>], including generating a patente [<xref ref-type="bibr" rid="scirp.102537-ref20">20</xref>]. β-carotene, lycopene, and astaxanthin are among the carotenoids described and used as photoprotection due to their antioxidant action, which acts against free radicals induced by UV radiation to protect the skin against erythema [<xref ref-type="bibr" rid="scirp.102537-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref21">21</xref>].</p><p>In this context, the present work sought to summarize the characteristics of carotenoids, their structures, properties, classifications, sources of obtention, commercialization, and applications. Besides, this review addresses the production of carotenoids from extremophilic microorganisms, especially from the Caatinga Domain, as a promising source of these biomolecules with interesting properties; as well as, they envision their applications in cosmetic products, especially those with UV protection.</p></sec><sec id="s2"><title>2. Carotenoids</title><sec id="s2_1"><title>2.1. Molecular Structure</title><p>Natural lipophilic pigments, known for their diversity of structures, carotenoids originate from the biosynthetic pathway of terpenoids [<xref ref-type="bibr" rid="scirp.102537-ref22">22</xref>]. These compounds present in their basic structure eight isoprenoid units joined in such a way that the molecule has inverted symmetry in the center. They have linear structures that are, in general, derived from a C<sub>40</sub>H<sub>56</sub> acyclic chain with a system of double and single bonds distributed along its length [<xref ref-type="bibr" rid="scirp.102537-ref23">23</xref>].</p><p>This system acts as a chromophore and is one of the most striking features of the structure of carotenoids [<xref ref-type="bibr" rid="scirp.102537-ref22">22</xref>]. The length of the chromophore and the presence or absence of functions determine the absorption spectrum. Also, the color of the molecule, besides giving these pigments a high chemical reactivity, can be easily isomerized and oxidized [<xref ref-type="bibr" rid="scirp.102537-ref24">24</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref25">25</xref>].</p><p>There were characterized about 500 structures. More than 95% of carotenoids are formed by a chain of 40 carbons, which is known as tetraterpenoids. Also, there are groups formed by 30 and 50 carbon atoms [<xref ref-type="bibr" rid="scirp.102537-ref26">26</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref27">27</xref>].</p><p>From this diversity of structures, carotenoids naturally have different physical, chemical, functional properties, and even stability [<xref ref-type="bibr" rid="scirp.102537-ref25">25</xref>]. Some of these properties were described by these authors are shown in <xref ref-type="fig" rid="fig1">Figure 1</xref>.</p></sec><sec id="s2_2"><title>2.2. Classification and Diversity of Carotenoids</title><p>Carotenoids are classified into two large groups according to the characteristics of their molecular structures:</p><p>&#173; Carotenes: molecular formula C<sub>40</sub>H<sub>56</sub>, which include α, β, γ-carotenes, and lycopene;</p><p>&#173; Xanthophylls: oxygenated and hydroxylated derivatives of carotenes, which include cryptoxanthin (C<sub>40</sub>H<sub>55</sub>OH) and lutein (C<sub>40</sub>H<sub>54</sub>(OH)<sub>2</sub>).</p><p>This classification occurs according to the absence or presence of oxygen atoms [<xref ref-type="bibr" rid="scirp.102537-ref28">28</xref>].</p><p>Carotenes are characterized by its composition, only of carbon and hydrogen (pure hydrocarbons), which can be cyclized at one or both molecule extremities, while xanthophylls are oxygen-substituting groups, (hydroxy, methoxy, carboxy, keto and epoxy groups) that generate many structural derivatives and higher polarity when compared to carotenes (<xref ref-type="fig" rid="fig2">Figure 2</xref>) [<xref ref-type="bibr" rid="scirp.102537-ref29">29</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref30">30</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref31">31</xref>].</p><p>Isomerization and oxidation of trans carotenoids (stable form in nature) to the cis form (loss of color and activity) can occur with the modification of the basic acyclic structure C40 by hydrogenation, dehydrogenation, cyclization or oxidation, generating great variability of carotenoids [<xref ref-type="bibr" rid="scirp.102537-ref31">31</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref32">32</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref33">33</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref34">34</xref>]. The most commonly found in nature and food are β-carotene, α-carotene, β-cryptoxanthin, lycopene, lutein, violaxanthin, and zeaxanthin; due to this availability, they are the most studied in terms of biological activities that help in health promotion [<xref ref-type="bibr" rid="scirp.102537-ref35">35</xref>].</p></sec></sec><sec id="s3"><title>3. Application and Commercialization of Carotenoids in Industrial Products</title><p>Commercial production of carotenoids has been developed, since 1954. They have been, since then, used as a food coloring and nutritional supplements. Also, they help to maintain the aromas and vitamins of foods [<xref ref-type="bibr" rid="scirp.102537-ref36">36</xref>]. Besides, they are used in the production of margarine and butter, fruit juices and drinks, soups, dairy products, as well as in fish, desserts, sugar, salad dressings, meats, pasta, eggs, and mayonnaise industries [<xref ref-type="bibr" rid="scirp.102537-ref37">37</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref37">37</xref>]. These biomolecules are also added in animal feed, in aquaculture, for example, they are sources of pigmentation for fish and crustaceans [<xref ref-type="bibr" rid="scirp.102537-ref34">34</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref39">39</xref>]. This sector of animal feed is the sector with the highest growth, and it is estimated that it will comprise the largest carotenoid market in 2023, according to the Global Carotenoid Market [<xref ref-type="bibr" rid="scirp.102537-ref5">5</xref>].</p><p>Carotenoids can be used in various ways in the pharmaceutical and medical industry, such as pro-biotic, syrups, antimicrobial agents, for controlling diseases, and in the modulation of immunological reactions. For environmental purposes, they are used as bioindicators, as well as they are applied in the cosmetics industry for the production of protectors, tanners, creams, among other products [<xref ref-type="bibr" rid="scirp.102537-ref37">37</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref38">38</xref>].</p><p>According to Cutzu et al. [<xref ref-type="bibr" rid="scirp.102537-ref40">40</xref>], the total value of carotenoids in the global market has an annual growth of 2.3%. According to BCC [<xref ref-type="bibr" rid="scirp.102537-ref41">41</xref>], in 2017, it was expected to reach $1.5 billion, and forecasts for 2022 will be $2.0 billion. In the period between 2007 and 2017, the value increased twice, since the estimated global scale value in 2007 was 766 million dollars. This growth, in the market, has been driven by the properties of carotenoids, global megatrend of the amplification of carotenoids use, demand for applications, and growing interest in developing processes to efficiently produce these pigments [<xref ref-type="bibr" rid="scirp.102537-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref40">40</xref>].</p><p>Initially and until 2016, the global manufacturing industry for this group of dyes was dominated by suppliers from Europe, such as the United Kingdom, Switzerland, Germany, France, Italy, the Netherlands, and Spain. However, in recent years, the Asia-Pacific region has been growing and receiving investments and research initiatives for the use of carotenoids [<xref ref-type="bibr" rid="scirp.102537-ref17">17</xref>]. The main industrial producers identified in the global carotenoid market are BASF SE (Germany), Hoffmann-La Roche (Switzerland), Royal DSM NV (Netherlands), Chr. Hansen A/S (Denmark), FMC Corporation (USA), Kemin Industries, Inc. (USA), and Cyanotech Corporation (USA) [<xref ref-type="bibr" rid="scirp.102537-ref5">5</xref>]. They produce and commercialize different carotenoids such as β-carotene, canthaxanthin, astaxanthin, apocarotenoids, and citranaxanthin [<xref ref-type="bibr" rid="scirp.102537-ref24">24</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref42">42</xref>].</p></sec><sec id="s4"><title>4. Microbiological Production of Carotenoids</title><p>Due to the global demand for natural dyes, there is an increasing preference for pigments of microbial origin, and being produced for the food industry, textile dyeing, pharmaceuticals, and cosmetics [<xref ref-type="bibr" rid="scirp.102537-ref17">17</xref>]. This search has resulted in constant research regarding the production of microbial carotenoids in biotechnological processes [<xref ref-type="bibr" rid="scirp.102537-ref36">36</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref43">43</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref44">44</xref>]. Carotenoids are synthesized by some bacteria, filamentous fungi, yeasts, and microalgae, which have few commercially exploited species [<xref ref-type="bibr" rid="scirp.102537-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref25">25</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref45">45</xref>].</p><p>Production of carotenoids by microorganisms demonstrates a safe use. Also, it has been an area of intense investigation since it allows the obtaining of the compounds of natural origin on an industrial scale, which is being considered a promising production strategy [<xref ref-type="bibr" rid="scirp.102537-ref25">25</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref43">43</xref>].</p><p>This type of production has some advantages, as it is a fast, highly efficient process that can be easily managed during production. At the same time, it is superior in versatility and productivity and is independent of climatic conditions when compared to production from fruits and vegetables [<xref ref-type="bibr" rid="scirp.102537-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref46">46</xref>]. Finally, it is possible to produce different shades of color with a relatively easy procedure for extracting and separating cell biomass. Also, the microorganisms can grow on cheap substrates [<xref ref-type="bibr" rid="scirp.102537-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref25">25</xref>].</p><p>To further increase yields and guarantee the production of microbial carotenoids, studies have been carried out on processes to optimizing cultivation conditions, the use of cheap substrates, and genetic engineering studies [<xref ref-type="bibr" rid="scirp.102537-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref17">17</xref>].</p><p>Despite the large number of microbial carotenoids already identified and characterized, only a few are produced on an industrial scale. Also, the market for carotenoids synthesized by bioprocesses is still a little difficult to estimate. It is due to the lack of statistics on regional low-tech products or because production is dispersed in small companies around the world.</p><p>Among the products already available on the market obtained through microbially, there is astaxanthin produced by the yeast Phaffia rhodozyma, the bacterium Agrobacterium auranticum, and the freshwater microalgae Haematococcus pluvialis [<xref ref-type="bibr" rid="scirp.102537-ref25">25</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref47">47</xref>], also β-carotene synthesized by Blakeslea trispora and zeaxanthin produced by Flavobacterium. It also stands out the production of β-carotene, torulene, and torularodine by yeasts of the genus Rhodotorula [<xref ref-type="bibr" rid="scirp.102537-ref25">25</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref47">47</xref>]. Besides, these microbial pigments are considered safe and approved by the Food and Drug Administration (FDA) [<xref ref-type="bibr" rid="scirp.102537-ref17">17</xref>].</p><p>Much research is been directed to find new sources of this group of pigments, which has promising properties, and strategies that can increase the efficiency of these biotechnological systems. So, these dyes are commercially viable and can be expanded in the various industrial sectors [<xref ref-type="bibr" rid="scirp.102537-ref40">40</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref48">48</xref>].</p></sec><sec id="s5"><title>5. Biotechnological Potential of the Caatinga Domain</title><p>The Caatinga domain has the most extreme meteorological values in Brazil. It has the strongest sunshine, the lowest cloudiness, low annual precipitation rates (below 800 mm), and high daytime temperatures, which can vary between 23˚C and 27˚C, while the soil can reach temperatures close to 60˚C [<xref ref-type="bibr" rid="scirp.102537-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref14">14</xref>].</p><p>This region is of fundamental importance in the life of local communities. It offers a wide variety of plants that are used for medicinal purposes, and that explicit the potential of this domain for research studies of new bioactive products [<xref ref-type="bibr" rid="scirp.102537-ref49">49</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref50">50</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref51">51</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref52">52</xref>].</p><p>Among the compounds produced by some plants in the Caatinga and identified by their beneficial biological actions to health, there are carotenoids. In a study by David et al. [<xref ref-type="bibr" rid="scirp.102537-ref53">53</xref>], there was possible to correlate the antioxidant and cytotoxic activity with the presence of β-carotenes in Caatinga plants. The greatest activities were observed in Passiflora cincinnata, Chamaecrista repens, Rollinia leptopetala, Serjania glabrata, Diospyros gaultheriifolia, and Mimosa ophtalmocentra.</p><p>Another source of carotenoids in the Caatinga is carotenogenic microorganisms, but little is known about them since most studies describe the carotenoids synthesized by plants, as well as their respective biological activities. In a group of bacteria, for example, the information obtained is that only 1% of bacteria in this domain (including pigmented and non-pigmented ones) have already been discovered and described [<xref ref-type="bibr" rid="scirp.102537-ref54">54</xref>]. However, after the publication of this percentage, referring to groups of microorganisms in the Caatinga Domain and their carotenogenic potentials, there is a scarcity of these data in literature over the years.</p><p>Thus, as it constitutes an environment with interesting biotechnological potential and with little information in the field of microbial bioprospecting, greater attention is needed to the Caatinga and the development of more studies [<xref ref-type="bibr" rid="scirp.102537-ref55">55</xref>]; since, it presents a vast diversity of microorganisms, little explored and in which new natural carotenoid producers can be discovered.</p>Microorganisms Isolated from the Caatinga Domain as New Sources of Carotenoids<p>Microorganisms isolated from environments that present extreme conditions are considered hostile or extreme [<xref ref-type="bibr" rid="scirp.102537-ref56">56</xref>]. To guarantee their survival, they develop biochemical mechanisms and produce metabolites to overcome these unfavorable factors. An example of this efficient strategy is the synthesis of carotenoid pigments to minimize the effects of oxidative damage on cells and other damage caused by high sun exposure [<xref ref-type="bibr" rid="scirp.102537-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref16">16</xref>].</p><p>The soil of these arid or semi-arid environments, considered as a hostile or extreme environment, is recognized as a rich habitat. It has microorganisms that produce natural molecules with biotechnological potential, whose biological activities are extremely rich and still poorly explored [<xref ref-type="bibr" rid="scirp.102537-ref55">55</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref57">57</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref58">58</xref>].</p><p>Microorganisms most found in the soil microbiota of this environment belong to the phylum Actinobacteria, which perform essential functions for the ecological balance of this habitat [<xref ref-type="bibr" rid="scirp.102537-ref59">59</xref>]. This group grows in extreme conditions, such as soils with low moisture content, typical of semi-arid regions, as well as being representative in terms of richness and diversity [<xref ref-type="bibr" rid="scirp.102537-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref58">58</xref>]. They produce pigments of different colors such as carotenoids, which characterize the group and contribute to environmental resistance. They also produce extracellular enzymes and important secondary metabolites [<xref ref-type="bibr" rid="scirp.102537-ref55">55</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref60">60</xref>].</p><p>In a study by Ramos et al. [<xref ref-type="bibr" rid="scirp.102537-ref15">15</xref>], the pigment production and chromogenic diversity of soil actinobacteria from the semiarid region of Cear&#225; state were evaluated. It classifies some strains according to color. Also, it suggests the presence of some genera described in the literature as carotenoid producers; characterized by a yellow color, the genera Actinoplanes, Agrococcus, Arsenicicoccus, Cellulomonas, Kocuria, Microbacterium, Rhodococcus, Serinicoccus, Streptomyces were found, and as representatives of the pink color Arthrobacter and Gordonia. It can be seen among these genera, that the majority was responsible for the production of yellow carotenoids. According to Kampe et al. [<xref ref-type="bibr" rid="scirp.102537-ref61">61</xref>] and Kavamura et al. [<xref ref-type="bibr" rid="scirp.102537-ref62">62</xref>], this color is characteristic of a microbiota specialized in biomolecules with photoprotective properties. Also, they have structures that contribute to these properties.</p><p>As actinobacteria, the presence of some yeasts in the microbiota of these hostile Brazilian environments also stands out. Da Silva Andrade et al. [<xref ref-type="bibr" rid="scirp.102537-ref63">63</xref>], showed that from the yeast, Rhodotorula glutinis, isolated at the semi-arid Pernambucano soil, β-carotene can be obtained by using economical production conditions. Also, the ability of this carotenoid to inhibit cell growth of tumor cells was evaluated and effective for breast cancer and promyelocytic leukemia.</p><p>These data corroborate with the idea that the Caatinga Domain is a potential source of microorganisms that produce promising molecules, especially carotenoids. Also, it will be a region of great interest to biotechnologists, which has prospects for applications in industries.</p></sec><sec id="s6"><title>6. Application of Carotenoids in the Cosmetics Industry</title><p>Chemical UV filters do not fully protect the skin, as they absorb, instead of reflecting or spreading all the UV photons that reach the skin. Most of the consequences caused by UVA radiation are related to the generation of Reactive Oxygen Species (ROS) after exposure. Therefore, it is necessary to add antioxidant molecules to sunscreens, especially in topical products, which minimize UV damage to the skin [<xref ref-type="bibr" rid="scirp.102537-ref64">64</xref>].</p><p>Carotenoids have aroused the interest of the cosmetic industries, since they are important natural antioxidants acting in the reduction of the generation of free radicals and, consequently, diminish the photodamage in the skin [<xref ref-type="bibr" rid="scirp.102537-ref65">65</xref>]. Also, they have a promising anti-UV capability, which boosts the development of photoprotective cosmetic formulations [<xref ref-type="bibr" rid="scirp.102537-ref3">3</xref>]. Whereas, it is intended to reduce the concentration of chemical filters or replace them with sunscreens based on natural products [<xref ref-type="bibr" rid="scirp.102537-ref26">26</xref>].</p><p>β-carotene, lycopene, and astaxanthin are among the most described carotenoids and used as photo protectors since they have strong antioxidant properties [<xref ref-type="bibr" rid="scirp.102537-ref21">21</xref>]. β-carotene, known as a precursor to provitamin A, a strong inhibitor of <sup>1</sup>O<sub>2</sub>, and free radical scavenger is strongly associated with its accumulation in the skin after ingestion, and later, its transformation into vitamin A in the body, which helps in the formation of melanin [<xref ref-type="bibr" rid="scirp.102537-ref66">66</xref>].</p><p>Lycopene, a potent antioxidant, has a significant correlation in skin roughness. It suggests that higher levels of skin antioxidants effectively can reduce skin roughness [<xref ref-type="bibr" rid="scirp.102537-ref66">66</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref67">67</xref>]. Astaxanthin acts as an effective antioxidant against lipid peroxidation and oxidative stress. Also, this property is associated with the prevention of the formation of spots and wrinkles on human skin [<xref ref-type="bibr" rid="scirp.102537-ref66">66</xref>].</p><p>However, the application of these carotenoids at the topical level is still poorly investigated; they are normally produced commercially for oral use. Studies with cosmetics formulations, which use these molecules, demonstrate interesting results as far as oral ingestion, reinforcing the approach of using topical carotenoids to prevent oxidative stress induced by acute UV exposure. Also, it supplies cutaneous levels of antioxidants, among other benefits [<xref ref-type="bibr" rid="scirp.102537-ref66">66</xref>] [<xref ref-type="bibr" rid="scirp.102537-ref68">68</xref>].</p><p>Carotenoids extracted from microorganisms have been stimulating their applications in formulations of sunscreens and other anti-UV products since they have powerful antioxidant properties, solubility, and stability in oil emulsions. Rare carotenoids with excellent properties can be isolated as well as the carotenoids used traditionally [<xref ref-type="bibr" rid="scirp.102537-ref19">19</xref>], which makes them attractive even for the production of patents [<xref ref-type="bibr" rid="scirp.102537-ref20">20</xref>].</p><p>In this context, due to the extreme conditions described above, the microorganisms isolated from the Caatinga Domain present themselves as promising sources of carotenoids little studied, which stimulates their use in cosmetic products. Also, the production of these molecules is induced by strong UV exposure, which demonstrates interesting antioxidant and photoprotective properties.</p><p>Thus, as future perspectives, bioprospecting research in the Caatinga should be strongly encouraged. It will allow an increase in the number of natural resources of carotenoids, and even investigate those considered rare and poorly described. Therefore, based on these data, actions and strategies for the economic use of these molecules can be defined, with the generation of biotechnological products with applications both in the cosmetics industry and in other industrial sectors; through its technology without harming the natural relationships of the environment and preserving its biodiversity [<xref ref-type="bibr" rid="scirp.102537-ref69">69</xref>].</p></sec><sec id="s7"><title>Acknowledgements</title><p>The authors are grateful for the financial support of the Coordena&#231;&#227;o de Aperfei&#231;oamento de Pessoal de N&#237;vel Superior ou Educa&#231;&#227;o (CAPES).</p></sec><sec id="s8"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s9"><title>Cite this paper</title><p>de C&#225;ssia Dias Mendes-Silva, T., da Silva Andrade, R.F., Ootani, M.A., Mendes, P.V.D., de Queiroz Cavalcanti de S&#225;, R.A., da Silva, M.R.F., Souza, K.S., dos Santos Correia, M.T., da Silva, M.V. and de Oliveira, M.B.M. (2020) Biotechnological Potential of Carotenoids Produced by Extremophilic Microorganisms and Application Prospects for the Cosmetics Industry. Advances in Microbiology, 10, 397-410. https://doi.org/10.4236/aim.2020.108029</p></sec></body><back><ref-list><title>References</title><ref id="scirp.102537-ref1"><label>1</label><mixed-citation publication-type="book" xlink:type="simple">Kaczor, A., Barańska, M. and Czamara, K. (2016) Carotenoids: Overview of Nomenclature, Structures, Occurrence and Functions. In: Kaczor, A. and Baranska, M., Eds., Carotenoids: Nutrition, Analysis and Technology, John Wiley &amp; Sons, Ltd., Hoboken, 1-13. https://doi.org/10.1002/9781118622223.ch1</mixed-citation></ref><ref id="scirp.102537-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Carle, R. and Schweiggert, R. (2016) Handbook on Natural Pigments in Food and Beverages: Industrial Applications for Improving Food Color. Woodhead Publishing, Sawston.</mixed-citation></ref><ref id="scirp.102537-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Ram, S., Mitra, M., Shah, F., Tirkey, S.R. and Mishra, S. (2020) Bacteria as an Alternate Biofactory for Carotenoid Production: A Review of Its Applications, Opportunities and Challenges. Journal of Functional Foods, 67, Article ID: 103867. https://doi.org/10.1016/j.jff.2020.103867</mixed-citation></ref><ref id="scirp.102537-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Wang, N., Manabe, Y., Sugawara, T., Paul, N.A. and Zhao, J. (2018) Identification and Biological Activities of Carotenoids from the Freshwater Alga Oedogonium intermedium. Food Chemistry, 242, 247-255.https://doi.org/10.1016/j.foodchem.2017.09.075</mixed-citation></ref><ref id="scirp.102537-ref5"><label>5</label><mixed-citation publication-type="book" xlink:type="simple">Bogacz-Radomska, L., Harasym, J. and Piwowar, A. (2020) Commercialization Aspects of Carotenoids. In: Galanakis, C.K., Ed., Carotenoids: Properties, Processing and Applications, Elsevier, Amsterdam, 327-357. https://doi.org/10.1016/B978-0-12-817067-0.00010-5</mixed-citation></ref><ref id="scirp.102537-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Valduga, E., Tatsch, P.O., Tiggemann, L., Treichel, H., Toniazzo, G., Zeni, J., Di Luccio, M. and Furigo, A. (2009) Produ&amp;#231;&amp;#227;o de carotenoides: Microrganismos como fonte de pigmentos naturais. Química Nova, 32, 2429-2436. https://doi.org/10.1590/S0100-40422009000900036</mixed-citation></ref><ref id="scirp.102537-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Ribeiro, J.E.S., Da Silva Sant’Ana, A.M., Martini, M., Sorce, C., Andreucci, A., De Melo, D.J.N. and Da Silva, F.L.H. (2019) Rhodotorula glutinis Cultivation on Cassava Wastewater for Carotenoids and Fatty Acids Generation. Biocatalysis and Agricultural Biotechnology, 22, Article ID: 101419. https://doi.org/10.1016/j.bcab.2019.101419</mixed-citation></ref><ref id="scirp.102537-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Mussagy, C.U., Winterburn, J., Santos-Ebinuma, V.C. and Pereira, J.F.B. (2019) Production and Extraction of Carotenoids Produced by Microorganisms. Applied Microbiology and Biotechnology, 103, 1095-1114. https://doi.org/10.1007/s00253-018-9557-5</mixed-citation></ref><ref id="scirp.102537-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Torregrosa-Crespo, J., Montero, Z., Fuentes, J.L., Reig García-Galbis, M., Garbayo, I., Vílchez, C. and Martínez-Espinosa, R.M. (2018) Exploring the Valuable Carotenoids for the Large-Scale Production by Marine Microorganisms. Marine Drugs, 16, 203. https://doi.org/10.3390/md16060203</mixed-citation></ref><ref id="scirp.102537-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Malik, K., Tokkas, J. and Goyal, S. (2012) Microbial Pigments: A Review. International Journal of Microbial Resource Technology, 1, 361-365.</mixed-citation></ref><ref id="scirp.102537-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Canganella, F. and Wiegel, J. (2011) Extremophiles: From Abyssal to Terrestrial Ecosystems and Possibly beyond. Naturwissenschaften, 98, 253-279. https://doi.org/10.1007/s00114-011-0775-2</mixed-citation></ref><ref id="scirp.102537-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Da Silva Andrade, R.F., Lima, R.A., Ribeaux, D.R., Waleska, H., Araújo, C., Franco, L.O., Pessoa-Júnior, A. and Campos-Takaki, G.M. (2016) Production of β-Carotene by a Newly Isolated Rhodotorula glutinis UCP1555 Strain and Cytotoxic Effect Evaluation. Journal of Chemistry, 10, 212-220. https://doi.org/10.17265/1934-7375/2016.05.003</mixed-citation></ref><ref id="scirp.102537-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Freitas, J.V., Lopes, N.P. and Gaspar, L.R. (2015) Photostability Evaluation of Five UV-Filters, Trans-Resveratrol and Beta-Carotene in Sunscreens. European Journal of Pharmaceutical Sciences, 78, 79-89. https://doi.org/10.1016/j.ejps.2015.07.004</mixed-citation></ref><ref id="scirp.102537-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Terao, J., Minami, Y. and Bando, N. (2010) Singlet Molecular Oxygen-Quenching Activity of Carotenoids: Relevance to Protection of the Skin from Photoaging. Journal of Clinical Biochemistry and Nutrition, 48, 57-62. https://doi.org/10.3164/jcbn.11-008FR</mixed-citation></ref><ref id="scirp.102537-ref15"><label>15</label><mixed-citation publication-type="book" xlink:type="simple">Tosato, M.G., Orallo, D.E., Fangio, M.F., Diz, V., Dicelio, L.E. and Churio, M.S. (2016) Nanomaterials and Natural Products for UV-Photoprotection. In: Grumezescu, A.M., Ed., Surface Chemistry of Nanobiomaterials, Elsevier, Amsterdam, 359-392. https://doi.org/10.1016/B978-0-323-42861-3.00012-1</mixed-citation></ref><ref id="scirp.102537-ref16"><label>16</label><mixed-citation publication-type="other" xlink:type="simple">Darvin, M., Patzelt, A., Gehse, S., Schanzer, S., Benderoth, C., Sterry, W. and Lademann, J. (2008) Cutaneous Concentration of Lycopene Correlates Significantly with the Roughness of the Skin. European Journal of Pharmaceutics and Biopharmaceutics, 69, 943-947. https://doi.org/10.1016/j.ejpb.2008.01.034</mixed-citation></ref><ref id="scirp.102537-ref17"><label>17</label><mixed-citation publication-type="other" xlink:type="simple">Silva, V., Martins, C.M. and Silveira, S.C. (2015) Atividade celulolítica de actinobactérias de regi&amp;#227;o semiárida do Ceará. Enciclopédia Biosfera, 11, 2026-2036.https://doi.org/10.18677/Enciclopedia_Biosfera_2015_016</mixed-citation></ref><ref id="scirp.102537-ref18"><label>18</label><mixed-citation publication-type="other" xlink:type="simple">Loiola, M.I.B., De Araújo Roque, A. and De Oliveira, A.C.P. (2012) Caatinga: Vegeta&amp;#231;&amp;#227;o do semiárido brasileiro. Notas Técnicas, 4, 14-19.</mixed-citation></ref><ref id="scirp.102537-ref19"><label>19</label><mixed-citation publication-type="other" xlink:type="simple">Kavamura, V.N., Taketani, R.G., Lan&amp;#231;oni, M.D., andreote, F.D., Mendes, R. and De Melo, I.S. (2013) Water Regime Influences Bulk Soil and Rhizosphere of Cereus jamacaru Bacterial Communities in the Brazilian Caatinga Biome. PLoS ONE, 8, e73606.</mixed-citation></ref><ref id="scirp.102537-ref20"><label>20</label><mixed-citation publication-type="other" xlink:type="simple">Kampe, B., R&amp;#246;sch, P. and Popp, J. (2015) Characterization of Carotenoids in Soil Bacteria and investigation of Their Photodegradation by UVA Radiation via Resonance Raman Spectroscopy. Analyst, 140, 4584-4593. https://doi.org/10.1039/C5AN00438A</mixed-citation></ref><ref id="scirp.102537-ref21"><label>21</label><mixed-citation publication-type="other" xlink:type="simple">Amsaveni, R., Sureshkumar, M., Vivekanandhan, G., Bhuvaneshwari, V., Kalaiselvi, M., Padmalochana, K. and Preethikaharshini, J. (2015) Screening and Isolation of Pigment Producing Actinomycetes from Soil Samples. International Journal of Biosciences, 2, 24-28.</mixed-citation></ref><ref id="scirp.102537-ref22"><label>22</label><mixed-citation publication-type="other" xlink:type="simple">Da Silva, I.L., Coel, L.C.B.B. and Da Silva, L.A.D.O. (2015) Biotechnological Potential of the Brazilian Caatinga Biome. Advances in Research, 5, 1-17.</mixed-citation></ref><ref id="scirp.102537-ref23"><label>23</label><mixed-citation publication-type="other" xlink:type="simple">Silva, V., Martins, C.M. and Silveira, S.C. (2015) Atividade celulolítica de actinobactérias de regi&amp;#227;o semiárida do Ceará. Enciclopédia Biosfera, 11, 2026-2036.https://doi.org/10.18677/Enciclopedia_Biosfera_2015_016</mixed-citation></ref><ref id="scirp.102537-ref24"><label>24</label><mixed-citation publication-type="other" xlink:type="simple">Duarte, R.T., Nóbrega, F., Nakayama, C.R. and Pellizari, V.H. (2012) Brazilian Research on Extremophiles in the Context of astrobiology. International Journal of astrobiology, 11, 325-333. https://doi.org/10.1017/S1473550412000249</mixed-citation></ref><ref id="scirp.102537-ref25"><label>25</label><mixed-citation publication-type="other" xlink:type="simple">Tian, B. and Hua, Y. (2010) Carotenoid Biosynthesis in Extremophilic Deinococcus-Thermus Bacteria. Trends in Microbiology, 18, 512-520. https://doi.org/10.1016/j.tim.2010.07.007</mixed-citation></ref><ref id="scirp.102537-ref26"><label>26</label><mixed-citation publication-type="other" xlink:type="simple">Rodrigues, J.P., Prova, S.S., Moraes, L.A.B. and Ifa, D.R. (2018) Characterization and Mapping of Secondary Metabolites of Streptomyces sp. from Caatinga by Desorption Electrospray Ionization Mass Spectrometry (DESI-MS). Analytical and Bioanalytical Chemistry, 410, 7135-7144. https://doi.org/10.1007/s00216-018-1315-0</mixed-citation></ref><ref id="scirp.102537-ref27"><label>27</label><mixed-citation publication-type="other" xlink:type="simple">Martin, V.J., Pitera, D.J., Withers, S.T., Newman, J.D. and Keasling, J.D. (2003) Engineering a Mevalonate Pathway in Escherichia coli for Production of Terpenoids. Nature Biotechnology, 21, 796-802. https://doi.org/10.1038/nbt833</mixed-citation></ref><ref id="scirp.102537-ref28"><label>28</label><mixed-citation publication-type="other" xlink:type="simple">David, J.P., Meira, M., David, J.M., Brand&amp;#227;o, H.N., Branco, A., De Fátima Agra, M., Barbosa, M.R.V., De Queiroz, L.P. and Giulietti, A.M. (2007) Radical Scavenging, Antioxidant and Cytotoxic Activity of Brazilian Caatinga Plants. Fitoterapia, 78, 215-218. https://doi.org/10.1016/j.fitote.2006.11.015</mixed-citation></ref><ref id="scirp.102537-ref29"><label>29</label><mixed-citation publication-type="other" xlink:type="simple">Do Nascimento Magalh&amp;#227;es, K., Guarniz, W.A.S., Sá, K.M., Freire, A.B., Monteiro, M.P., Nojosa, R.T., Bieski, I.G.C., Custódio, J.B., Balogun, S.O. and Bandeira, M.A.M. (2019) Medicinal Plants of the Caatinga, Northeastern Brazil: Ethnopharmacopeia (1980-1990) of the Late Professor Francisco José de Abreu Matos. Journal of Ethnopharmacology, 237, 314-353.https://doi.org/10.1016/j.jep.2019.03.032</mixed-citation></ref><ref id="scirp.102537-ref30"><label>30</label><mixed-citation publication-type="other" xlink:type="simple">Santos, M.O., Ribeiro, D.A., Macêdo, D.G., Macedo, M.J., Macedo, J.G., Lacerda, M.N.S., Macedo, M.S., Souza, M. and Maria, A. (2018) Medicinal Plants: Versatility and Concordance of Use in the Caatinga Area, Northeastern Brazil. Anais da Academia Brasileira de Ciências, 90, 2767-2779. https://doi.org/10.1590/0001-3765201820170594</mixed-citation></ref><ref id="scirp.102537-ref31"><label>31</label><mixed-citation publication-type="other" xlink:type="simple">Santos, M.O., Almeida, B.V., Ribeiro, D.A., Macêdo, D.G., Macedo, M.J., Macedo, J.G., Sousa, F.F.D., Oliveira, L.G.D., Saraiva, M.E. and Araujo, T. (2017) The Conservation of Native Priority Medicinal Plants in a Caatinga Area in Ceará, Northeastern Brazil. Anais da Academia Brasileira de Ciências, 89, 2675-2685. https://doi.org/10.1590/0001-3765201720160633</mixed-citation></ref><ref id="scirp.102537-ref32"><label>32</label><mixed-citation publication-type="other" xlink:type="simple">Ceravolo, I.P., Zani, C.L., Figueiredo, F.J., Kohlhoff, M., Santana, A.E. and Krettli, A.U. (2018) Aspidosperma Pyrifolium, a Medicinal Plant from the Brazilian Caatinga, Displays a High Antiplasmodial Activity and Low Cytotoxicity. Malaria Journal, 17, Article No. 436. https://doi.org/10.1186/s12936-018-2568-y</mixed-citation></ref><ref id="scirp.102537-ref33"><label>33</label><mixed-citation publication-type="book" xlink:type="simple">Ahmad, W.A., Ahmad, W.Y.W., Zakaria, Z.A. and Yusof, N.Z. (2012) Application of Bacterial Pigments as Colorant. In: Ahmad, W.A., Ahmad, W.Y.W., Zakaria, Z.A. and Yusof, N.Z., Eds., Application of Bacterial Pigments as Colorant, Springer, Berlin, 57-74. https://doi.org/10.1007/978-3-642-24520-6_4</mixed-citation></ref><ref id="scirp.102537-ref34"><label>34</label><mixed-citation publication-type="other" xlink:type="simple">Krinsky, N.I. (1994) The Biological Properties of Carotenoids. Pure and Applied Chemistry, 66, 1003-1010. https://doi.org/10.1351/pac199466051003</mixed-citation></ref><ref id="scirp.102537-ref35"><label>35</label><mixed-citation publication-type="other" xlink:type="simple">Sy, C., Dangles, O., Borel, P. and Caris-Veyrat, C. (2015) Stability of Bacterial Carotenoids in the Presence of Iron in a Model of the Gastric Compartment—Comparison with Dietary Reference Carotenoids. Archives of Biochemistry and Biophysics, 572, 89-100. https://doi.org/10.1016/j.abb.2014.12.030</mixed-citation></ref><ref id="scirp.102537-ref36"><label>36</label><mixed-citation publication-type="book" xlink:type="simple">Kopec, R.E., Cooperstone, J.L., Cichon, M.J. and Schwartz, S.J. (2012) Analysis Methods of Carotenoids. In: Xu, Z.M. and Luke, R., Eds., Howard Analysis of Antioxidant-Rich Phytochemicals, Wiley-Blackwell, Hoboken, 105-149. https://doi.org/10.1002/9781118229378.ch4</mixed-citation></ref><ref id="scirp.102537-ref37"><label>37</label><mixed-citation publication-type="other" xlink:type="simple">Rês, M.V., Francheschi, E., Borges, G.R., Dariva, C., De Castilhos Corazza, F., Oliveira, J.V. and Corazza, M.L. (2007) Influência da temperatura na solubilidade de β-Caroteno em solventes organicos à press&amp;#227;o ambiente. Food Science and Technology, 27, 737-743. https://doi.org/10.1590/S0101-20612007000400011</mixed-citation></ref><ref id="scirp.102537-ref38"><label>38</label><mixed-citation publication-type="other" xlink:type="simple">Bonadio, M.D.P., Freita, L.A.D. and Mutton, M.J.R. (2018) Carotenoid Production in Sugarcane Juice and Synthetic Media Supplemented with Nutrients by Rhodotorula rubra L02. Brazilian Journal of Microbiology, 49, 872-878. https://doi.org/10.1016/j.bjm.2018.02.010</mixed-citation></ref><ref id="scirp.102537-ref39"><label>39</label><mixed-citation publication-type="other" xlink:type="simple">Hamerski, L., Rezende, M.J.C. and Da Silva, B.V. (2013) Usando as cores da natureza para atender aos desejos do consumidor: Substancias naturais como corantes na indústria alimentícia. Revista Virtual de Química, 5, 394-420.</mixed-citation></ref><ref id="scirp.102537-ref40"><label>40</label><mixed-citation publication-type="other" xlink:type="simple">BCC Research (2018) The Global Market for Carotenoids. https://www.bccresearch.com/market-research/food-and-beverage/carotenoids-market-fod025c.html</mixed-citation></ref><ref id="scirp.102537-ref41"><label>41</label><mixed-citation publication-type="other" xlink:type="simple">Cutzu, R., Coi, A., Rosso, F., Bardi, L., Ciani, M., Budroni, M., Zara, G., Zara, S. and Mannazzu, I. (2013) from Crude Glycerol to Carotenoids by Using a Rhodotorula glutinis Mutant. World Journal of Microbiology and Biotechnology, 29, 1009-1017. https://doi.org/10.1007/s11274-013-1264-x</mixed-citation></ref><ref id="scirp.102537-ref42"><label>42</label><mixed-citation publication-type="other" xlink:type="simple">Aksu, Z. and Eren, A.T. (2007) Production of Carotenoids by the Isolated Yeast of Rhodotorula glutinis. Biochemical Engineering Journal, 35, 107-113. https://doi.org/10.1016/j.bej.2007.01.004</mixed-citation></ref><ref id="scirp.102537-ref43"><label>43</label><mixed-citation publication-type="other" xlink:type="simple">Latha, B. and Jeevaratanm, K. (2012) Thirteen-Week Oral Toxicity Study of Carotenoid Pigment from Rhodotorula glutinis DFR-PDY in Rats. Indian Journal of Experimental Biology, 50, 645-651.</mixed-citation></ref><ref id="scirp.102537-ref44"><label>44</label><mixed-citation publication-type="other" xlink:type="simple">El-Banna, A.A., El-Razek, A.M.A. and El-Mahdy, A.R. (2012) Some Factors Affecting the Production of Carotenoids by Rhodotorula glutinis var. glutinis. Food and Nutrition Sciences, 3, 64-71. https://doi.org/10.4236/fns.2012.31011</mixed-citation></ref><ref id="scirp.102537-ref45"><label>45</label><mixed-citation publication-type="other" xlink:type="simple">Marova, I., Haronikova, A., Petrik, S., Dvorakova, T. and Breierova, E. (2012) Production of Enriched Biomass by Red Yeasts of Sporobolomyces sp. Grown on Waste Substrates. The Journal of Microbiology, Biotechnology and Food Sciences, 1, 534.</mixed-citation></ref><ref id="scirp.102537-ref46"><label>46</label><mixed-citation publication-type="other" xlink:type="simple">Yang, M., Wang, Y., Liu, Q., Liu, Z., Jiang, F., Wang, H., Guo, X., Zhang, J. and Kang, L. (2019) A β-Carotene-Binding Protein Carrying a Red Pigment Regulates Body-Color Transition between Green and Black in Locusts. eLife, 8, e41362. https://doi.org/10.7554/eLife.41362</mixed-citation></ref><ref id="scirp.102537-ref47"><label>47</label><mixed-citation publication-type="other" xlink:type="simple">Schroeder, W.A. and Johnson, E.A. (1995) Singlet Oxygen and Peroxyl Radicals Regulate Carotenoid Biosynthesis in Phaffia rhodozyma. Journal of Biological Chemistry, 270, 18374-18379. https://doi.org/10.1074/jbc.270.31.18374</mixed-citation></ref><ref id="scirp.102537-ref48"><label>48</label><mixed-citation publication-type="book" xlink:type="simple">Provesi, J.G. and Amante, E.R. (2015) Carotenoids in Pumpkin and Impact of Processing Treatments and Storage. In: Preedy, V., Ed., Processing and Impact on Active Components in Food, Elsevier, Amsterdam, 71-80. https://doi.org/10.1016/B978-0-12-404699-3.00009-3</mixed-citation></ref><ref id="scirp.102537-ref49"><label>49</label><mixed-citation publication-type="other" xlink:type="simple">Gomes, F.D.S. (2007) Carotenóides: Uma possível prote&amp;#231;&amp;#227;o contra o desenvolvimento de cancer. Revista de Nutri&amp;#231;&amp;#227;o, 20, 537-548. https://doi.org/10.1590/S1415-52732007000500009</mixed-citation></ref><ref id="scirp.102537-ref50"><label>50</label><mixed-citation publication-type="other" xlink:type="simple">Ngamwonglumlert, L., Devahastin, S. and Chiewchan, N. (2017) Natural Colorants: Pigment Stability and Extraction Yield Enhancement via Utilization of Appropriate Pretreatment and Extraction Methods. Critical Reviews in Food Science and Nutrition, 57, 3243-3259. https://doi.org/10.1080/10408398.2015.1109498</mixed-citation></ref><ref id="scirp.102537-ref51"><label>51</label><mixed-citation publication-type="book" xlink:type="simple">Moliné, M., Libkind, D. and Van Broock, M. (2012) Production of Torularhodin, Torulene, and β-Carotene by Rhodotorula Yeasts. In: Barredo, J.L., Ed., Microbial Carotenoids from fungi, Humana Press, Totowa, 275-283. https://doi.org/10.1007/978-1-61779-918-1_19</mixed-citation></ref><ref id="scirp.102537-ref52"><label>52</label><mixed-citation publication-type="other" xlink:type="simple">Botella-Pavía, P. and Rodríguez-Concepción, M. (2006) Carotenoid Biotechnology in Plants for Nutritionally Improved Foods. Physiologia Plantarum, 126, 369-381.https://doi.org/10.1111/j.1399-3054.2006.00632.x</mixed-citation></ref><ref id="scirp.102537-ref53"><label>53</label><mixed-citation publication-type="other" xlink:type="simple">Amorim-Carrilho, K., Cepeda, A., Fente, C. and Regal, P. (2014) Review of Methods for Analysis of Carotenoids. TrAC Trends in Analytical Chemistry, 56, 49-73. https://doi.org/10.1016/j.trac.2013.12.011</mixed-citation></ref><ref id="scirp.102537-ref54"><label>54</label><mixed-citation publication-type="other" xlink:type="simple">Rodriguez-Amaya, D.B. (2015) Food Carotenoids: Chemistry, Biology and Technology. John Wiley &amp; Sons, Hoboken. https://doi.org/10.1002/9781118864364</mixed-citation></ref><ref id="scirp.102537-ref55"><label>55</label><mixed-citation publication-type="other" xlink:type="simple">Heider, S.A., Peters-Wendisch, P., Wendisch, V.F., Beekwilder, J., Brautaset, T. (2014) Metabolic Engineering for the Microbial Production of Carotenoids and Related Products with a Focus on the Rare C50 Carotenoids. Applied Microbiology and Biotechnology, 98, 4355-4368. https://doi.org/10.1007/s00253-014-5693-8</mixed-citation></ref><ref id="scirp.102537-ref56"><label>56</label><mixed-citation publication-type="other" xlink:type="simple">Kirti, K., Amita, S., Priti, S., Kumar, A.M. and Jyoti, S. (2014) Colorful World of Microbes: Carotenoids and Their Applications. Advances in Biology, 2014, Article ID: 837891. https://doi.org/10.1155/2014/837891</mixed-citation></ref><ref id="scirp.102537-ref57"><label>57</label><mixed-citation publication-type="other" xlink:type="simple">Britton, G. (1995) Structure and Properties of Carotenoids in Relation to Function. The FASEB Journal, 9, 1551-1558. https://doi.org/10.1096/fasebj.9.15.8529834</mixed-citation></ref><ref id="scirp.102537-ref58"><label>58</label><mixed-citation publication-type="other" xlink:type="simple">Aryee, A.N., Agyei, D. and Akanbi, T.O. (2018) Recovery and Utilization of Seaweed Pigments in Food Processing. Current Opinion in Food Science, 19, 113-119. https://doi.org/10.1016/j.cofs.2018.03.013</mixed-citation></ref><ref id="scirp.102537-ref59"><label>59</label><mixed-citation publication-type="other" xlink:type="simple">Rodriguez-Amaya, D.B. (2019) Update on Natural Food Pigments-A Mini-Review on Carotenoids, Anthocyanins, and Betalains. Food Research International, 124, 200-205. https://doi.org/10.1016/j.foodres.2018.05.028</mixed-citation></ref><ref id="scirp.102537-ref60"><label>60</label><mixed-citation publication-type="other" xlink:type="simple">Stahl, W. and Sies, H. (2012) β-Carotene and Other Carotenoids in Protection from Sunlight. The American Journal of Clinical Nutrition, 96, 1179S-1184S. https://doi.org/10.3945/ajcn.112.034819</mixed-citation></ref><ref id="scirp.102537-ref61"><label>61</label><mixed-citation publication-type="other" xlink:type="simple">Goks&amp;#248;yr, A. (2013) Carotenoid Sunscreen. Google Patents.</mixed-citation></ref><ref id="scirp.102537-ref62"><label>62</label><mixed-citation publication-type="other" xlink:type="simple">Netzer, R., Stafsnes, M.H., Andreassen, T., Goks&amp;#248;yr, A., Bruheim, P. and Brautaset, T. (2010) Biosynthetic Pathway for γ-Cyclic Sarcinaxanthin in Micrococcus luteus: Heterologous Expression and Evidence for Diverse and Multiple Catalytic Functions of C50 Carotenoid Cyclases. Journal of Bacteriology, 192, 5688-5699. https://doi.org/10.1128/JB.00724-10</mixed-citation></ref><ref id="scirp.102537-ref63"><label>63</label><mixed-citation publication-type="other" xlink:type="simple">Martins, A., Tenreiro, T., Andrade, G., Gadanho, M., Chaves, S., Abrantes, M., Calado, P., Tenreiro, R. and Vieira, H. (2013) Photoprotective Bioactivity Present in a Unique Marine Bacteria Collection from Portuguese Deep Sea Hydrothermal Vents. Marine Drugs, 11, 1506-1523. https://doi.org/10.3390/md11051506</mixed-citation></ref><ref id="scirp.102537-ref64"><label>64</label><mixed-citation publication-type="other" xlink:type="simple">Venil, C.K., Zakaria, Z.A. and Ahmad, W.A. (2013) Bacterial Pigments and Their Applications. Process Biochemistry, 48, 1065-1079. https://doi.org/10.1016/j.procbio.2013.06.006</mixed-citation></ref><ref id="scirp.102537-ref65"><label>65</label><mixed-citation publication-type="other" xlink:type="simple">Sharma, M., Dangi, P. and Choudhary, M. (2014) Actinomycetes: Source, Identification, and Their Applications. International Journal of Current Microbiology and Applied Sciences, 3, 801-832.</mixed-citation></ref><ref id="scirp.102537-ref66"><label>66</label><mixed-citation publication-type="other" xlink:type="simple">Ramos, K.A., De Brito, F.A.E., Janielle, K., Nunes, F., Martins, C.M. and Martins, S.C.S. (2015) Caracteriza&amp;#231;&amp;#227;o e diversidade cromogênica de actinobactérias de um nicho microbiano preservado no bioma Caatinga. Enciclopédia Biosfera, 11, 2115-2125.</mixed-citation></ref><ref id="scirp.102537-ref67"><label>67</label><mixed-citation publication-type="other" xlink:type="simple">Menezes, K.A.S., De Oliveira Nunes, G.F., Sampaio, A.A., De Tarso Aidar, S., Martins, L.M.V. and Fernandes-Júnior, P.I. (2015) Seedling Development of Nodulating and Non-Nodulating Native Legumes in Soils from Brazilian Caatinga Biome. Plant Science Today, 2, 56-59. https://doi.org/10.14719/pst.2015.2.2.97</mixed-citation></ref><ref id="scirp.102537-ref68"><label>68</label><mixed-citation publication-type="other" xlink:type="simple">Souto, P.C., Souto, J.S., Santos, R.V.D., Bakke, I.A., Sales, F.D.C.V. and Souza, B.V.D. (2013) Taxa de decomposi&amp;#231;&amp;#227;o da serapilheira e atividade microbiana em área de Caatinga. Cerne, 19, 559-565. https://doi.org/10.1590/S0104-77602013000400005</mixed-citation></ref><ref id="scirp.102537-ref69"><label>69</label><mixed-citation publication-type="other" xlink:type="simple">Apgaua, D.M.G., Dos Santos, R.M., Pereira, D.G.S., De Oliveira Menino, G.C., Pires, G.G., Fontes, M.A.L. and Tng, D.Y.P. (2014) Beta-Diversity in Seasonally Dry Tropical Forests (SDTF) in the Caatinga Biogeographic Domain, Brazil, and Its Implications for Conservation. Biodiversity and Conservation, 23, 217-232. https://doi.org/10.1007/s10531-013-0599-9</mixed-citation></ref></ref-list></back></article>