首页 > 最新文献

Progress in Biological Sciences最新文献

英文 中文
Phosphate: the Silent Challenge 磷酸盐:无声的挑战
Pub Date : 2014-05-01 DOI: 10.22059/PBS.2014.50302
M. Malboobi, Katayoun Zamani, T. Lohrasebi, M. Sarikhani, Ali Samaian, M. S. Sabet
Phosphorus (P) is one of the most vital elements for all living organisms which acts as aconstituent of essential biomolecules such as nucleic acids, phospholipids, and phosphosugars,and as a major contributor to almost all metabolic reactions including photosynthesis,respiration, and energy delivery. It is one of the most needed nutrients for plant growth anddevelopment. Despite high levels of P in the soil, plants absorb it only in the soluble inorganicform of free phosphate ion (Pi) which is scarce in soil. Therefore, there has been a large demandfor Pi fertilizers to secure crop yields, yet its deposition in soil and gradual run-off into waterreservoirs lead to chains of events that cause irreversible damages to ecosystems. Researches,including genome-wide data analyses, have revealed interesting molecular aspects of plantadaptive strategies to deal with low Pi concentrations in soil. These include the higherexpression of acid phosphatases and Pi transporters as well as the secretion of organic acids inthe rhizosphere that maintain cellular Pi homeostasis in order to keep metabolic reactionsrunning. Describing the cycle of Pi exchange between physical and biological worlds, the extentto which current agricultural practices are disturbing the cycle, the necessity of introducing lessdestructivemethods of providing Pi, and alternative measures and solutions for sustainableagriculture will be discussed in this review.
磷(P)是所有生物体中最重要的元素之一,是核酸、磷脂和磷酸糖等必需生物分子的组成部分,也是几乎所有代谢反应的主要贡献者,包括光合作用、呼吸作用和能量传递。它是植物生长发育最需要的营养物质之一。尽管土壤中磷含量很高,但植物仅以土壤中稀缺的可溶性无机形式游离磷离子(Pi)吸收磷。因此,为了确保作物产量,对磷肥的需求量很大,但其在土壤中的沉积和逐渐流入水库导致了一系列事件,对生态系统造成了不可逆转的损害。包括全基因组数据分析在内的研究揭示了植物适应策略的有趣分子方面,以应对土壤中低浓度的Pi。这些包括酸性磷酸酶和Pi转运蛋白的高表达,以及根际有机酸的分泌,这些有机酸维持细胞Pi稳态,以保持代谢反应的运行。本文将讨论物理世界和生物世界之间的Pi交换周期,当前农业实践对该周期的干扰程度,引入破坏性较小的提供Pi方法的必要性,以及可持续农业的替代措施和解决方案。
{"title":"Phosphate: the Silent Challenge","authors":"M. Malboobi, Katayoun Zamani, T. Lohrasebi, M. Sarikhani, Ali Samaian, M. S. Sabet","doi":"10.22059/PBS.2014.50302","DOIUrl":"https://doi.org/10.22059/PBS.2014.50302","url":null,"abstract":"Phosphorus (P) is one of the most vital elements for all living organisms which acts as aconstituent of essential biomolecules such as nucleic acids, phospholipids, and phosphosugars,and as a major contributor to almost all metabolic reactions including photosynthesis,respiration, and energy delivery. It is one of the most needed nutrients for plant growth anddevelopment. Despite high levels of P in the soil, plants absorb it only in the soluble inorganicform of free phosphate ion (Pi) which is scarce in soil. Therefore, there has been a large demandfor Pi fertilizers to secure crop yields, yet its deposition in soil and gradual run-off into waterreservoirs lead to chains of events that cause irreversible damages to ecosystems. Researches,including genome-wide data analyses, have revealed interesting molecular aspects of plantadaptive strategies to deal with low Pi concentrations in soil. These include the higherexpression of acid phosphatases and Pi transporters as well as the secretion of organic acids inthe rhizosphere that maintain cellular Pi homeostasis in order to keep metabolic reactionsrunning. Describing the cycle of Pi exchange between physical and biological worlds, the extentto which current agricultural practices are disturbing the cycle, the necessity of introducing lessdestructivemethods of providing Pi, and alternative measures and solutions for sustainableagriculture will be discussed in this review.","PeriodicalId":20726,"journal":{"name":"Progress in Biological Sciences","volume":"201 1","pages":"1-32"},"PeriodicalIF":0.0,"publicationDate":"2014-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80160693","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 8
Study of the inhibitory effect of the media culture parameters and cell population to increase the biomass production of Dunaliella tertiolecta 培养基培养参数和细胞群体对杜氏藻生物量增加抑制作用的研究
Pub Date : 2013-12-01 DOI: 10.22059/PBS.2013.35829
R. Taheri, M. Shariati
Microalgal growth curve, after the exponential phase, shows a stationary phase where algalbiomass production is inhibited and remains constant by some factors such as nutrientdepletion and intrinsic behavior. The present study is concerned with evaluating effects ofthe culture medium condition and intrinsic behavior on biomass production by Dunaliellatertiolecta. To this end, effect of pH, nutrient concentration, CO2 (NaHCO3) concentration,possible secreted substances, and cell density on the biomass production by D. tertiolectawere investigated. The results showed that biomass yield can be significantly affected by pH(p<0.01) and nutrient (p<0.05). In a combination of pH and nutrient, the biomass was found tobe more influenced by the pH, compared with the nutrients. The results showed a significantinteraction between nutrient and NaHCO3 (p<0.05), suggesting that CO2 concentration maylimit biomass production only when sufficient nutrients are available. Nutrients concentrationand biomass production showed a direct correlation (p<0.05). The rate of reaching themaximum biomass was showed to be increased in higher nutrients concentration; however,the maximum point could not to be affected. The existence of secreted compounds withinhibitory effect on the growth was not observed. The inhibitory effect of the cell density onbiomass production can not be confirmed.
微藻生长曲线在指数阶段之后,呈现出受营养耗竭和内在行为等因素抑制的稳定阶段。本文研究了培养基条件和内在行为对杜氏藻生物量产生的影响。为此,研究了pH、养分浓度、CO2 (NaHCO3)浓度、可能分泌的物质和细胞密度对D. tertiolectaa生物量的影响。结果表明:pH(p<0.01)和养分(p<0.05)对生物量产量有显著影响;在pH和养分组合的情况下,与养分相比,生物量受pH的影响更大。结果表明,营养物与NaHCO3之间存在显著的交互作用(p<0.05),表明CO2浓度只有在营养物充足的情况下才会限制生物量的生产。养分浓度与生物量呈显著正相关(p<0.05)。养分浓度越高,达到最大生物量的速率越高;但是,最大值不受影响。未观察到对生长有抑制作用的分泌物的存在。细胞密度对生物量产生的抑制作用尚未得到证实。
{"title":"Study of the inhibitory effect of the media culture parameters and cell population to increase the biomass production of Dunaliella tertiolecta","authors":"R. Taheri, M. Shariati","doi":"10.22059/PBS.2013.35829","DOIUrl":"https://doi.org/10.22059/PBS.2013.35829","url":null,"abstract":"Microalgal growth curve, after the exponential phase, shows a stationary phase where algalbiomass production is inhibited and remains constant by some factors such as nutrientdepletion and intrinsic behavior. The present study is concerned with evaluating effects ofthe culture medium condition and intrinsic behavior on biomass production by Dunaliellatertiolecta. To this end, effect of pH, nutrient concentration, CO2 (NaHCO3) concentration,possible secreted substances, and cell density on the biomass production by D. tertiolectawere investigated. The results showed that biomass yield can be significantly affected by pH(p<0.01) and nutrient (p<0.05). In a combination of pH and nutrient, the biomass was found tobe more influenced by the pH, compared with the nutrients. The results showed a significantinteraction between nutrient and NaHCO3 (p<0.05), suggesting that CO2 concentration maylimit biomass production only when sufficient nutrients are available. Nutrients concentrationand biomass production showed a direct correlation (p<0.05). The rate of reaching themaximum biomass was showed to be increased in higher nutrients concentration; however,the maximum point could not to be affected. The existence of secreted compounds withinhibitory effect on the growth was not observed. The inhibitory effect of the cell density onbiomass production can not be confirmed.","PeriodicalId":20726,"journal":{"name":"Progress in Biological Sciences","volume":"90 1","pages":"123-133"},"PeriodicalIF":0.0,"publicationDate":"2013-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83914828","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Phylogenetic and sequence analysis of the growth hormone gene of two sturgeons, Huso huso and Acipenser Gueldenstaedtii 两种中华鲟生长激素基因的系统发育及序列分析
Pub Date : 2013-12-01 DOI: 10.22059/PBS.2013.35827
L. A. Pormehr, M. Pourkazemi, M. Yarmohammadi, Yalda Banismaeili, M. Sanati
In this study, the cDNA Growth Hormone (cGH) of the Belugasturgeon (Husohuso) and Russian sturgeon (Acipensergueldenstaedtii) were cloned and sequenced, and phylogenetic relationships were examined using nucleic acid and amino acid sequences. The nucleotide sequence of the Beluga GH has an open reading frame of 645 nucleotides encoding a protein 214 amino acid residues. The signal peptide cleavage site was predicted to be at position 72, yeilding a signal peptide of 24aminoacid residues and a mature peptide of 190 amino acids. The cDNAsequence of the Russian sturgeon was similar to that of the Beluga cGH. The phylogenetic analysis was performed based on amino acid and DNA sequences using the neighbor oining(NJ) and Maximum parsimony (MP) method. Phylogenic trees by the two methods wereidentical in most of the clades with the high bootstrap support, and the topology of amino acid and DNA sequences showed highest similarity with mammalian sequences.
本研究对白鲟(Belugasturgeon, Husohuso)和俄罗斯鲟(Russian sturgeon, Acipensergueldenstaedtii)的cDNA生长激素(cDNA Growth Hormone, cGH)进行了克隆和测序,并利用核酸和氨基酸序列分析了它们的系统发育关系。白鲸GH的核苷酸序列具有645个核苷酸的开放阅读框,编码214个氨基酸残基的蛋白。信号肽裂解位点预计在72位,产生一个由24个氨基酸残基组成的信号肽和一个由190个氨基酸组成的成熟肽。俄罗斯鲟鱼的基因序列与白鲸的基因序列相似。采用邻域聚类法(NJ)和最大简约法(MP)对氨基酸和DNA序列进行系统发育分析。两种方法的系统发育树在大多数支系中具有较高的自举支持度,且氨基酸和DNA序列的拓扑结构与哺乳动物序列的相似性最高。
{"title":"Phylogenetic and sequence analysis of the growth hormone gene of two sturgeons, Huso huso and Acipenser Gueldenstaedtii","authors":"L. A. Pormehr, M. Pourkazemi, M. Yarmohammadi, Yalda Banismaeili, M. Sanati","doi":"10.22059/PBS.2013.35827","DOIUrl":"https://doi.org/10.22059/PBS.2013.35827","url":null,"abstract":"In this study, the cDNA Growth Hormone (cGH) of the Belugasturgeon (Husohuso) and Russian sturgeon (Acipensergueldenstaedtii) were cloned and sequenced, and phylogenetic relationships were examined using nucleic acid and amino acid sequences. The nucleotide sequence of the Beluga GH has an open reading frame of 645 nucleotides encoding a protein 214 amino acid residues. The signal peptide cleavage site was predicted to be at position 72, yeilding a signal peptide of 24aminoacid residues and a mature peptide of 190 amino acids. The cDNAsequence of the Russian sturgeon was similar to that of the Beluga cGH. The phylogenetic analysis was performed based on amino acid and DNA sequences using the neighbor oining(NJ) and Maximum parsimony (MP) method. Phylogenic trees by the two methods wereidentical in most of the clades with the high bootstrap support, and the topology of amino acid and DNA sequences showed highest similarity with mammalian sequences.","PeriodicalId":20726,"journal":{"name":"Progress in Biological Sciences","volume":"44 1","pages":"99-105"},"PeriodicalIF":0.0,"publicationDate":"2013-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91232670","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Changes of major wall polysaccharides and glycoproteins of tobacco cells in response to excess boron 过量硼对烟草细胞主要壁多糖和糖蛋白的影响
Pub Date : 2013-12-01 DOI: 10.22059/PBS.2013.35841
F. Ghanati, M. D. Heidarabadi
Effects of excess concentrations of boron on major cell wall components of tobacco cells(Nicotiana tabacum L. cv. Burley 21) were studied. Pectin, xyloglucan, hydroxyproline-richglycoproteins (extensin), and arabinogalactan proteins were characterized. Results showedthat increased boron supply resulted in significant decrease in cell and cell wall dry weights.Also, high concentrations of boron reduced relative amounts of major wall components.Compared with the normal conditions, increase in certain sugars in pectin (e.g., xylose andits methylated derivative) and decrease in glucose, arabinose, and rhamnose in those treatedcells with higher concentrations of boron was significant. The content of hydroxyprolinerichglycoproteins decreased when tobacco cells were supplied with higher concentrations ofboron. In these cells, increased ratio of protein to glycan part and increase in hydroxyl lysineamong other amino acids were noticeable. Amount of arabinogalactan proteins also decreasedas boron supply increased. Excess boron did not alter the composition and concentration ofamino acids of arabinogalactan; however, it remarkably increased xylose and glucose butdecreased galactose and arabinose concentrations.
过量硼对烟草细胞主要细胞壁成分的影响。对Burley 21)进行了研究。对果胶、木葡聚糖、富含羟基脯氨酸糖蛋白(延伸蛋白)和阿拉伯半乳聚糖蛋白进行了表征。结果表明,硼供应增加导致细胞和细胞壁干重显著降低。此外,高浓度硼降低了主要壁组分的相对数量。与正常条件相比,在那些处理过高浓度硼的细胞中,果胶中某些糖(例如木糖及其甲基化衍生物)的增加和葡萄糖、阿拉伯糖和鼠李糖的减少是显著的。当硼浓度升高时,烟草细胞中羟脯氨酸糖蛋白含量降低。在这些细胞中,蛋白质与聚糖部分的比例增加,其他氨基酸中羟基赖氨酸的增加是明显的。随着硼供应的增加,阿拉伯半乳聚糖蛋白的数量也减少。过量硼对阿拉伯半乳聚糖的氨基酸组成和浓度没有影响;然而,它显著提高了木糖和葡萄糖的浓度,但降低了半乳糖和阿拉伯糖的浓度。
{"title":"Changes of major wall polysaccharides and glycoproteins of tobacco cells in response to excess boron","authors":"F. Ghanati, M. D. Heidarabadi","doi":"10.22059/PBS.2013.35841","DOIUrl":"https://doi.org/10.22059/PBS.2013.35841","url":null,"abstract":"Effects of excess concentrations of boron on major cell wall components of tobacco cells(Nicotiana tabacum L. cv. Burley 21) were studied. Pectin, xyloglucan, hydroxyproline-richglycoproteins (extensin), and arabinogalactan proteins were characterized. Results showedthat increased boron supply resulted in significant decrease in cell and cell wall dry weights.Also, high concentrations of boron reduced relative amounts of major wall components.Compared with the normal conditions, increase in certain sugars in pectin (e.g., xylose andits methylated derivative) and decrease in glucose, arabinose, and rhamnose in those treatedcells with higher concentrations of boron was significant. The content of hydroxyprolinerichglycoproteins decreased when tobacco cells were supplied with higher concentrations ofboron. In these cells, increased ratio of protein to glycan part and increase in hydroxyl lysineamong other amino acids were noticeable. Amount of arabinogalactan proteins also decreasedas boron supply increased. Excess boron did not alter the composition and concentration ofamino acids of arabinogalactan; however, it remarkably increased xylose and glucose butdecreased galactose and arabinose concentrations.","PeriodicalId":20726,"journal":{"name":"Progress in Biological Sciences","volume":"19 1","pages":"27-38"},"PeriodicalIF":0.0,"publicationDate":"2013-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74465508","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Simple protocol for plant regeneration of Lilium ledebourii using transverse thin cell layer 利用横向薄细胞层再生百合植株的简单方案
Pub Date : 2013-12-01 DOI: 10.22059/PBS.2013.35828
M. Mirmasoumi, P. Azadi, A. Sharafi, Valentine Ntui Otang, M. Mii
Transverse thin cell layer sections excised from in vitro scales of Lilium ledebourii were cultured on Murashige and Skoog (MS) medium supplemented with various plant growth regulators (PGRs) at different concentrations. Although, bulblets were produced on PGRfree MS medium during organogenesis, addition of 0.25 mg l-1 6-benzyladenine or 5.0 mg l-1 indole-3-acetic acid to the medium increased the organogenesis response and produced 4.4 bulblets per explants. Two months later, the bulblets were transferred to MS PGRs-free medium. Bulblets were successfully transplanted to the soil after a cold treatment of 8 weeks,with a survival rate of 85%.
从百合离体鳞片上取下横向细胞薄层切片,分别在添加不同浓度植物生长调节剂(PGRs)的Murashige和Skoog (MS)培养基上进行培养。虽然在不含pgr0的MS培养基上产生了小球,但在培养基中添加0.25 mg l-1 6-苄基腺嘌呤或5.0 mg l-1吲哚-3-乙酸增加了器官发生反应,每个外植体产生4.4个小球。2个月后,将微球转移到无MS pgr的培养基中。经8周的低温处理后,小球茎成功移植到土壤中,成活率为85%。
{"title":"Simple protocol for plant regeneration of Lilium ledebourii using transverse thin cell layer","authors":"M. Mirmasoumi, P. Azadi, A. Sharafi, Valentine Ntui Otang, M. Mii","doi":"10.22059/PBS.2013.35828","DOIUrl":"https://doi.org/10.22059/PBS.2013.35828","url":null,"abstract":"Transverse thin cell layer sections excised from in vitro scales of Lilium ledebourii were cultured on Murashige and Skoog (MS) medium supplemented with various plant growth regulators (PGRs) at different concentrations. Although, bulblets were produced on PGRfree MS medium during organogenesis, addition of 0.25 mg l-1 6-benzyladenine or 5.0 mg l-1 indole-3-acetic acid to the medium increased the organogenesis response and produced 4.4 bulblets per explants. Two months later, the bulblets were transferred to MS PGRs-free medium. Bulblets were successfully transplanted to the soil after a cold treatment of 8 weeks,with a survival rate of 85%.","PeriodicalId":20726,"journal":{"name":"Progress in Biological Sciences","volume":"58 1","pages":"117-122"},"PeriodicalIF":0.0,"publicationDate":"2013-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90222265","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 13
An investigation on the effects of photoperiod, aging and culture media onvegetative growth and sporulation of rice blast pathogen pyricularia oryzae 光周期、老化和培养基对稻瘟病菌营养生长和产孢影响的研究
Pub Date : 2013-12-01 DOI: 10.22059/PBS.2013.35843
Mahdieh S. Hosseyni-Moghaddam, J. Soltani
Pyricularia oryzae (Tel. Magnaporthegrisea) is currently used as a fungal model for plantmicrobeinteraction studies as well as an indicative model for anticancer drug discovery. Thepresent study introduces the optimal condition in which P. oryzae grows and sporulates beston common culture media. We have considered three fungal culture media, i.e. PDA, PCA andWA, based on which P. oryzae sporulation inducers like rice polish, rice extract or rice leafsegments could be added, and evaluated both for vegetative growth and sporulation. Threelight regimens, i.e. continuous light, 16.8 hr light/darkness, and continuous darkness wereapplied in combination with nine synthetic culture media. Mycelial growth was measuredafter 11 days, but sporulation was tracked on the 10th, 20th, and 30th day after incubation at26oC. The findings indicate that PDA culture medium could provide the best medium for P.oryzae vegetative growth, regardless of light condition. However, P. oryzae could sporulatewhen light was provided either continuously or at intervals. A combination of 16.8 hr light/darkness intervals and adding rice materials to culture media could induce P. oryzae for abetter sporulation. RPCA can be used as the best culture medium for P. oryzae in order toobtain a high number of conidia under light alterations. Moreover, aging increases the totalnumber of conidia.
稻瘟病菌(pyricaria oryzae, Tel. Magnaporthegrisea)目前被用作植物微生物相互作用研究的真菌模型,以及抗癌药物发现的指示性模型。介绍了稻瘟病菌在普通培养基上生长和产孢的最佳条件。我们考虑了三种真菌培养基,即PDA, PCA和wa,在此基础上添加水稻粉,水稻提取物或水稻叶段等水稻芽孢诱导剂,并对营养生长和芽孢量进行了评估。三种光照方案,即连续光照、16.8小时光照/黑暗和连续黑暗,与9种合成培养基联合使用。11天后测量菌丝生长情况,并在26℃孵育后第10、20、30天追踪产孢情况。结果表明,无论光照条件如何,PDA培养基都是P.oryzae营养生长的最佳培养基。在连续光照和间歇光照条件下,稻瘟病菌均能产生孢子。在16.8 h光照/黑暗间隔和添加水稻材料的培养基中,可以诱导稻瘟病菌更好地产孢。RPCA可以作为水稻芽孢杆菌的最佳培养基,在光照条件下获得大量的分生孢子。此外,衰老使分生孢子总数增加。
{"title":"An investigation on the effects of photoperiod, aging and culture media onvegetative growth and sporulation of rice blast pathogen pyricularia oryzae","authors":"Mahdieh S. Hosseyni-Moghaddam, J. Soltani","doi":"10.22059/PBS.2013.35843","DOIUrl":"https://doi.org/10.22059/PBS.2013.35843","url":null,"abstract":"Pyricularia oryzae (Tel. Magnaporthegrisea) is currently used as a fungal model for plantmicrobeinteraction studies as well as an indicative model for anticancer drug discovery. Thepresent study introduces the optimal condition in which P. oryzae grows and sporulates beston common culture media. We have considered three fungal culture media, i.e. PDA, PCA andWA, based on which P. oryzae sporulation inducers like rice polish, rice extract or rice leafsegments could be added, and evaluated both for vegetative growth and sporulation. Threelight regimens, i.e. continuous light, 16.8 hr light/darkness, and continuous darkness wereapplied in combination with nine synthetic culture media. Mycelial growth was measuredafter 11 days, but sporulation was tracked on the 10th, 20th, and 30th day after incubation at26oC. The findings indicate that PDA culture medium could provide the best medium for P.oryzae vegetative growth, regardless of light condition. However, P. oryzae could sporulatewhen light was provided either continuously or at intervals. A combination of 16.8 hr light/darkness intervals and adding rice materials to culture media could induce P. oryzae for abetter sporulation. RPCA can be used as the best culture medium for P. oryzae in order toobtain a high number of conidia under light alterations. Moreover, aging increases the totalnumber of conidia.","PeriodicalId":20726,"journal":{"name":"Progress in Biological Sciences","volume":"18 1","pages":"135-143"},"PeriodicalIF":0.0,"publicationDate":"2013-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74366547","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 30
Population structure and variation in Persian sturgeon (Acipenser percicus ) from the Caspian Sea as determind from mitochondrial DNA sequences of the control region 对照区波斯鲟线粒体DNA序列测定里海波斯鲟种群结构和变异
Pub Date : 2013-12-01 DOI: 10.22059/PBS.2013.35826
S. Nazari, M. Pourkazemi, M. Khoshkholgh, Leila Azizzade
Mitochondria1 DNA (mtDNA) control region sequences were analyzed to evaluate the population genetic structure of Persian sturgeon (Acipenser persicus) in Caspian Sea. A total of 45 specimens were collected from the different locations of the Caspian Sea. MtDNA control region was amplified using PCR. Direct sequencing was performed according standard method. The results showed that 12 haplotypes were observed between 45 samples in the method. The highest numbers of haplotypes were observed in Sefidroud River in which 3 haplotypes A, B and E among them were specific for the river and were not observed in the other locations. The average haplotype diversity (h) and nucleotide diversity (π) were 0.795±0.037 and 0.0062±0.0046, respectively. The results of FST based on kimura- 2 parameters method and analysis of molecular variance (AMOVA) demonstrated that most variations occurred between samples from Sefidroud River in the south Caspian Sea and that the samples include three distinct populations including Sefidrud, Russia and Azerbaijan (P<0.001). As mtDNA control region is hypervariable segment, this can be provide potential marker for identifying probable populations and for determining their management and conservation units, leading to the useful application of molecular genetics in investigating conservation biology of the Persian sturgeon.
对里海波斯鲟(Acipenser persicus)线粒体DNA (mtDNA)控制区序列进行分析,评价其种群遗传结构。在里海的不同地点共收集了45个标本。采用PCR扩增MtDNA控制区。按标准方法直接测序。结果表明,该方法在45份样本中共检测到12个单倍型。单倍型数量最多的是Sefidroud River,其中A、B和E 3个单倍型为该河流所特有,在其他地区未见。平均单倍型多样性(h)和核苷酸多样性(π)分别为0.795±0.037和0.0062±0.0046。基于kimura- 2参数法和分子方差分析(AMOVA)的FST结果表明,里海南部塞菲德鲁德河样本间差异最大,包括塞菲德鲁德、俄罗斯和阿塞拜疆三个不同的种群(P<0.001)。由于mtDNA控制区是一个高变段,可以为鉴定可能的种群和确定其管理和保护单位提供潜在的标记,从而使分子遗传学在研究波斯鲟保护生物学中的有用应用。
{"title":"Population structure and variation in Persian sturgeon (Acipenser percicus ) from the Caspian Sea as determind from mitochondrial DNA sequences of the control region","authors":"S. Nazari, M. Pourkazemi, M. Khoshkholgh, Leila Azizzade","doi":"10.22059/PBS.2013.35826","DOIUrl":"https://doi.org/10.22059/PBS.2013.35826","url":null,"abstract":"Mitochondria1 DNA (mtDNA) control region sequences were analyzed to evaluate the population genetic structure of Persian sturgeon (Acipenser persicus) in Caspian Sea. A total of 45 specimens were collected from the different locations of the Caspian Sea. MtDNA control region was amplified using PCR. Direct sequencing was performed according standard method. The results showed that 12 haplotypes were observed between 45 samples in the method. The highest numbers of haplotypes were observed in Sefidroud River in which 3 haplotypes A, B and E among them were specific for the river and were not observed in the other locations. The average haplotype diversity (h) and nucleotide diversity (π) were 0.795±0.037 and 0.0062±0.0046, respectively. The results of FST based on kimura- 2 parameters method and analysis of molecular variance (AMOVA) demonstrated that most variations occurred between samples from Sefidroud River in the south Caspian Sea and that the samples include three distinct populations including Sefidrud, Russia and Azerbaijan (P<0.001). As mtDNA control region is hypervariable segment, this can be provide potential marker for identifying probable populations and for determining their management and conservation units, leading to the useful application of molecular genetics in investigating conservation biology of the Persian sturgeon.","PeriodicalId":20726,"journal":{"name":"Progress in Biological Sciences","volume":"42 1","pages":"67-80"},"PeriodicalIF":0.0,"publicationDate":"2013-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80602636","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 8
Saccharomyces cerevisiae TFS9, a novel isolated yeast capable of high caffeine-tolerant and its application in biodecaffeination approach 一种新型高咖啡因耐受性分离酵母及其在生物脱咖啡因方法中的应用
Pub Date : 2013-12-01 DOI: 10.22059/PBS.2013.35844
M. Ashengroph, M. Borchaluei
There is a great call for using microbial bio-decaffeination approach to remove caffeinefrom caffeinated products and industrial wastes. We aimed in this study to screen strainsof yeasts which exhibit high caffeine tolerance and to investigate the bio-degradation ofcaffeine under growth conditions. Sixteen yeast strains were isolated from the cultivatedtea soils collected from sites of northern Iran and evaluated for the caffeine tolerance bythe agar dilution method. Based on the tolerance efficiency, strain TFS9 was selected andidentified as Saccharomyces cerevisiae TFS9 (GenBank accession number KF414526)on the morphological and bioochemical characteristics as well as molecular phylogeneticstudies based on amplification the ITS1–5.8S–ITS2 rDNA sequences. The time course ofcaffeine removal by growing cells of the strain TFS9 in the minimal salt medium containingcaffeine as the sole source of carbon was estimated by a decrease in caffeine absorbanceusing UV-visible spectrophotometer. The concentration of caffeine in the supernatantof the yeast culture medium decreased by 84.8% (from 3.5g/l to 0.53 g/l) after 60h ofincubation by using of S. cerevisiae TFS9, without additional optimization process. Resultsof experimental studies suggest a simple and cost-effective process for the microbialdecaffeination of caffeine-containing solutions, and provide a promising approach fordeveloping safe processes that can be used effectively for decaffeination of industrialeffluents. The present study provides the first evidence on the caffeine bio-degradationusing yeast species of S. cerevisiae.
利用微生物脱咖啡因的方法从含咖啡因的产品和工业废物中去除咖啡因的呼声很高。本研究旨在筛选具有高咖啡因耐受性的酵母菌株,并研究其在生长条件下对咖啡因的生物降解。从伊朗北部茶叶栽培土壤中分离出16株酵母菌,用琼脂稀释法对其咖啡因耐受性进行了评价。根据菌株的耐受性,选择菌株TFS9,通过形态学和生化特征以及对ITS1-5.8S-ITS2 rDNA序列的扩增进行分子系统发育研究,鉴定菌株为Saccharomyces cerevisiae TFS9 (GenBank登录号KF414526)。用紫外可见分光光度计测定了菌株TFS9细胞在含咖啡因作为唯一碳源的最低盐培养基中去除咖啡因的时间过程。使用酿酒酵母TFS9培养60h后,酵母培养基上清液中咖啡因浓度下降84.8%(从3.5g/l降至0.53 g/l),无需再进行优化。实验研究的结果为含咖啡因溶液的微生物脱咖啡因提供了一种简单而经济的工艺,并为开发可有效用于工业废水脱咖啡因的安全工艺提供了一种有前途的方法。本研究首次提供了利用酿酒酵母对咖啡因进行生物降解的证据。
{"title":"Saccharomyces cerevisiae TFS9, a novel isolated yeast capable of high caffeine-tolerant and its application in biodecaffeination approach","authors":"M. Ashengroph, M. Borchaluei","doi":"10.22059/PBS.2013.35844","DOIUrl":"https://doi.org/10.22059/PBS.2013.35844","url":null,"abstract":"There is a great call for using microbial bio-decaffeination approach to remove caffeinefrom caffeinated products and industrial wastes. We aimed in this study to screen strainsof yeasts which exhibit high caffeine tolerance and to investigate the bio-degradation ofcaffeine under growth conditions. Sixteen yeast strains were isolated from the cultivatedtea soils collected from sites of northern Iran and evaluated for the caffeine tolerance bythe agar dilution method. Based on the tolerance efficiency, strain TFS9 was selected andidentified as Saccharomyces cerevisiae TFS9 (GenBank accession number KF414526)on the morphological and bioochemical characteristics as well as molecular phylogeneticstudies based on amplification the ITS1–5.8S–ITS2 rDNA sequences. The time course ofcaffeine removal by growing cells of the strain TFS9 in the minimal salt medium containingcaffeine as the sole source of carbon was estimated by a decrease in caffeine absorbanceusing UV-visible spectrophotometer. The concentration of caffeine in the supernatantof the yeast culture medium decreased by 84.8% (from 3.5g/l to 0.53 g/l) after 60h ofincubation by using of S. cerevisiae TFS9, without additional optimization process. Resultsof experimental studies suggest a simple and cost-effective process for the microbialdecaffeination of caffeine-containing solutions, and provide a promising approach fordeveloping safe processes that can be used effectively for decaffeination of industrialeffluents. The present study provides the first evidence on the caffeine bio-degradationusing yeast species of S. cerevisiae.","PeriodicalId":20726,"journal":{"name":"Progress in Biological Sciences","volume":"70 1","pages":"145-156"},"PeriodicalIF":0.0,"publicationDate":"2013-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86270223","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Optimal conditions for enhancing sodium dodecyl sulfate biodegradation by Pseudomonas aeruginosa KGS 铜绿假单胞菌KGS促进十二烷基硫酸钠生物降解的最佳条件
Pub Date : 2013-12-01 DOI: 10.22059/PBS.2013.35840
R. Shahbazi, R. Kasra-Kermanshahi, S. Gharavi, Z. M. Nejad, Faezeh Borzooee
The anionic surfactant sodium dodecyl sulfate (SDS) was degraded by novel strain ofPseudomonas aeruginosa KGS under accession No. JQ328193, which was isolated from carwash wastewater. The purpose of this research was to study different optimization conditionsrequired for enhancing the biodegradation of sodium dodecyl sulfate P. aeruginosa KGS.Influence of different Physicochemical factors such as nitrogen and carbon sources, pH,temperature, inoculation percent and different concentrations of SDS on the biodegradation ofSDS were investigated by measuring the degradation rate of SDS using methylene blue activesubstance (MBAS) method. The optimum conditions determined for the this selected bacteriumstrain for degradation of SDS were 1.5mM SDS, inoculation percent 7%, pH 7.5, temperature37°C, ammonium nitrate (nitrogen source) when basal salt medium was supplemented withglucose as a co substrate. This bacterium is able to degrade about 98% of the SDS after 24h ofincubation under optimized conditions of biodegradation. The results presented in this researchindicate that Pseudomonas aeruginosa is a suitable candidate for SDS biodegradation.
利用铜绿假单胞菌KGS菌株对阴离子表面活性剂十二烷基硫酸钠(SDS)进行降解。JQ328193,从洗车废水中分离得到。以十二烷基硫酸钠铜绿假单胞菌(P. aeruginosa kgs)为研究对象,通过亚甲基蓝活性物质(MBAS)法测定SDS的降解率,考察氮碳源、pH、温度、接种量和不同SDS浓度等不同理化因素对SDS生物降解的影响。该菌株对SDS的最佳降解条件为:1.5mM SDS,接种率7%,pH 7.5,温度37℃,硝酸铵(氮源),基础盐培养基中添加葡萄糖作为共底物。在优化的生物降解条件下,培养24小时后,该细菌可降解约98%的SDS。本研究结果表明,铜绿假单胞菌是SDS生物降解的合适候选者。
{"title":"Optimal conditions for enhancing sodium dodecyl sulfate biodegradation by Pseudomonas aeruginosa KGS","authors":"R. Shahbazi, R. Kasra-Kermanshahi, S. Gharavi, Z. M. Nejad, Faezeh Borzooee","doi":"10.22059/PBS.2013.35840","DOIUrl":"https://doi.org/10.22059/PBS.2013.35840","url":null,"abstract":"The anionic surfactant sodium dodecyl sulfate (SDS) was degraded by novel strain ofPseudomonas aeruginosa KGS under accession No. JQ328193, which was isolated from carwash wastewater. The purpose of this research was to study different optimization conditionsrequired for enhancing the biodegradation of sodium dodecyl sulfate P. aeruginosa KGS.Influence of different Physicochemical factors such as nitrogen and carbon sources, pH,temperature, inoculation percent and different concentrations of SDS on the biodegradation ofSDS were investigated by measuring the degradation rate of SDS using methylene blue activesubstance (MBAS) method. The optimum conditions determined for the this selected bacteriumstrain for degradation of SDS were 1.5mM SDS, inoculation percent 7%, pH 7.5, temperature37°C, ammonium nitrate (nitrogen source) when basal salt medium was supplemented withglucose as a co substrate. This bacterium is able to degrade about 98% of the SDS after 24h ofincubation under optimized conditions of biodegradation. The results presented in this researchindicate that Pseudomonas aeruginosa is a suitable candidate for SDS biodegradation.","PeriodicalId":20726,"journal":{"name":"Progress in Biological Sciences","volume":"40 1","pages":"107-115"},"PeriodicalIF":0.0,"publicationDate":"2013-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84964675","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Evaluation of effectiveness of some mitochondrial genes in biosystematics and phylogeographic studies of house mouse (Mus musculus ) subspecies 一些线粒体基因在家鼠亚种生物系统学和系统地理学研究中的有效性评价
Pub Date : 2013-12-01 DOI: 10.22059/PBS.2013.35825
Ahmadreza Katouzian, H. Rajabi-Maham
The identification of the efficiency of some mtDNA genes of Mus musculus species complex (house mouse) for biosystematics research was studied in this approach. Recent studies have made use of different mitochondrial genes including NADH dehydrogenase genes, cytochrome b gene, cytochrome oxidase genes, D-loop region and whole mtDNA genome to study the house mouse species. Usage of each of these genome regions has its own advantages and disadvantages. Identification of appropriate genomic regions is very important for molecular biosystematic research. We have shown here that NADH dehydrogenase and Cytochrome oxidase genes (particularly COX2) are especially useful in biosystematics studies and subspecies identification,whereas D-loop region is the best candidate for biogeographic and phylogeographic studiesof subspecies of this species efficiency-wise as well as economically. These candidates areintroduced considering that the first two gene complexes are highly conserved whereas the latteris well receptive to gaining and preserving the mutations through time.
用该方法研究了小家鼠物种复合体(家鼠)部分mtDNA基因在生物系统学研究中的有效性。近年来的研究利用NADH脱氢酶基因、细胞色素b基因、细胞色素氧化酶基因、d -环区和线粒体dna全基因组等不同的线粒体基因对家鼠进行了研究。每个基因组区域的使用都有其自身的优点和缺点。鉴定合适的基因组区域对分子生物系统研究非常重要。我们已经证明,NADH脱氢酶和细胞色素氧化酶基因(特别是COX2)在生物系统学研究和亚种鉴定中特别有用,而d环区是该物种亚种的生物地理和系统地理研究的最佳候选者,无论从效率还是经济角度来看都是如此。考虑到前两个基因复合物是高度保守的,而后者随着时间的推移很容易获得和保存突变,因此介绍了这些候选基因。
{"title":"Evaluation of effectiveness of some mitochondrial genes in biosystematics and phylogeographic studies of house mouse (Mus musculus ) subspecies","authors":"Ahmadreza Katouzian, H. Rajabi-Maham","doi":"10.22059/PBS.2013.35825","DOIUrl":"https://doi.org/10.22059/PBS.2013.35825","url":null,"abstract":"The identification of the efficiency of some mtDNA genes of Mus musculus species complex (house mouse) for biosystematics research was studied in this approach. Recent studies have made use of different mitochondrial genes including NADH dehydrogenase genes, cytochrome b gene, cytochrome oxidase genes, D-loop region and whole mtDNA genome to study the house mouse species. Usage of each of these genome regions has its own advantages and disadvantages. Identification of appropriate genomic regions is very important for molecular biosystematic research. We have shown here that NADH dehydrogenase and Cytochrome oxidase genes (particularly COX2) are especially useful in biosystematics studies and subspecies identification,whereas D-loop region is the best candidate for biogeographic and phylogeographic studiesof subspecies of this species efficiency-wise as well as economically. These candidates areintroduced considering that the first two gene complexes are highly conserved whereas the latteris well receptive to gaining and preserving the mutations through time.","PeriodicalId":20726,"journal":{"name":"Progress in Biological Sciences","volume":"9 1","pages":"39-66"},"PeriodicalIF":0.0,"publicationDate":"2013-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88147180","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
期刊
Progress in Biological Sciences
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1