Engineering transgenic Populus with enhanced biomass, wood quality and pest resistance through dual gene expression

IF 10.5 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Plant Biotechnology Journal Pub Date : 2025-01-24 DOI:10.1111/pbi.14590
Dian Wang, Fumei Liu, Mengyan Zhao, Xihao Yu, Jiping Feng, Wei Wang, Mengzhu Lu, Wei Li, Xianfeng Tang, Congpeng Wang, Gongke Zhou
{"title":"Engineering transgenic Populus with enhanced biomass, wood quality and pest resistance through dual gene expression","authors":"Dian Wang,&nbsp;Fumei Liu,&nbsp;Mengyan Zhao,&nbsp;Xihao Yu,&nbsp;Jiping Feng,&nbsp;Wei Wang,&nbsp;Mengzhu Lu,&nbsp;Wei Li,&nbsp;Xianfeng Tang,&nbsp;Congpeng Wang,&nbsp;Gongke Zhou","doi":"10.1111/pbi.14590","DOIUrl":null,"url":null,"abstract":"<p>Wood, one of the most abundant renewable natural resources globally, plays a crucial role in the timber, papermaking and bioenergy industries (Chutturi <i>et al</i>., <span>2023</span>). Wood (i.e. secondary xylem) is derived from vascular cambium, which is pivotal in determining the wood biomass in woody plants (Tang <i>et al</i>., <span>2022</span>). Reactive oxygen species (ROS) act as signalling molecules that regulate plant development, growth and responses to abiotic and biotic stresses (Wang <i>et al</i>., <span>2024</span>). Numerous studies underscore the significance of ROS in maintaining the root and shoot stem cell niches (Wang <i>et al</i>., <span>2024</span>). A recent study has indicated that LATERAL ORGAN BOUNDARIES DOMAIN 11 (LBD11) governs several ROS metabolic genes to manage the specific distribution of ROS within the cambium, thus affecting cambial cell proliferation in <i>Arabidopsis</i> root and shoot (Dang <i>et al</i>., <span>2023</span>). However, there remains a lack of clarity on the biological functions of ROS accumulation in tree vascular cambium activity. Additionally, the localized accumulation of ROS is required for lignin biosynthesis (Wang <i>et al</i>., <span>2024</span>). Therefore, ROS homeostasis enables woody plants to fine-tune the activity of cambium, increase wood yield and improve their quality.</p><p>In plants, various forms of ROS exist, including singlet oxygen (<sup>1</sup>O<sub>2</sub>), superoxide anion (O<sub>2</sub><sup>·−</sup>), hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>), hydroxyl radical (HO<sup>·</sup>) and others. Among them, O<sub>2</sub><sup>·−</sup> and H<sub>2</sub>O<sub>2</sub> play a crucial role in regulating stem cell fate in shoot apical meristem (SAM) and root apical meristem (RAM) (Wang <i>et al</i>., <span>2024</span>). Superoxide dismutases (SODs) are a group of metalloenzymes that scavenge ROS by converting O<sub>2</sub><sup>·−</sup> radicals into H<sub>2</sub>O<sub>2</sub>. In SAM and RAM, the balance between O<sub>2</sub><sup>·−</sup> and H<sub>2</sub>O<sub>2</sub> plays a critical role in the maintenance and differentiation of stem cells (Zeng <i>et al</i>., <span>2017</span>). Since the development of vascular cambium originates from the peripheral region of SAM, the balance between O<sub>2</sub><sup>·−</sup> and H<sub>2</sub>O<sub>2</sub> may also contribute significantly to vascular cambium activity. In this study, 11 <i>SOD</i> genes were identified in <i>Populus</i> genome (Figure S1). As revealed by the cell-type transcriptome analysis of the poplar stem (Dai <i>et al</i>., <span>2023</span>), among the 11 <i>SOD</i> genes, <i>CSD2</i> has a higher specific expression level in the cambium other than in the xylem or phloem, indicating a potential role of <i>CSD2</i> in vascular cambium development (Figure 1a).</p><p>To assess the effect of PdCSD2 on wood formation, the <i>PdCSD2</i> overexpression (OE) lines with substantially elevated <i>PdCSD2</i> transcript levels were developed in this study (Figure S2). Compared to the wild type (WT), the <i>PdCSD2</i>-OE lines exhibited a significant enhancement of growth with about a 10% increase in height and about a 20% increase in stem diameter (Figure 1b; Figure S3). Analysis of stem cross-sections revealed a 30% rise in the number of cambium cell layers at the 20th internode of <i>PdCSD2OE</i> plants in comparison to WT (Figure 1c; Figure S4). Accordingly, the xylem width at the 20th internode in <i>PdCSD2OE</i> plants was increased by approximately 20% relative to WT. Therefore, <i>PdCSD2OE</i> significantly enhances the wood biomass (Figure 1c; Figure S4). Numerous studies have demonstrated the essential role of ROS in regulating secondary cell wall formation, including lignin and cellulose biosynthesis and deposition (Dang <i>et al</i>., <span>2023</span>; Wang <i>et al</i>., <span>2024</span>). The overexpression of the SOD enzyme encoding gene <i>PdCSD2</i> is suspected to affect ROS accumulation and thus lignin content in xylem. To investigate the effect of PdCSD2 on lignin biosynthesis and xylem cell wall lignification, the xylem of the 20th internode of poplar was stained with phloroglucinol–HCl solution. A diminished staining intensity was observed in <i>PdCSD2-OE</i> plants compared to WT, as discovered for the growth of 1-year-old transgenic plants in fields (Figure 1d; Figure S11). Accordingly, the lignin content in the 20th internodes was reduced by 15% compared to that of WT (Figure 1e). These results provide evidence supporting the association between ROS and lignin biosynthesis. To investigate the effect of ROS on cellulose biosynthesis, pontamine fast scarlet 4B (S4B) staining was conducted on xylem sections of <i>PdCSD2OE</i> and WT plants. An increased staining intensity in <i>PdCSD2OE</i> xylem was observed, indicating elevated cellulose levels (Figure 1d). Furthermore, quantification of cellulose content revealed at least 15% higher cellulose content in <i>PdCSD2OE</i> plants compared to WT (Figure 1f). To evaluate the potential differences in the crystalline cellulose content of <i>PdCSD2OE</i> xylem, whole-mount immunolabelling assays were performed on the xylem section using a family 3 carbohydrate-binding module (CBM3a) antibody that specifically targets crystalline cellulose. The fluorescence intensity was found to be significantly enhanced in the sections of <i>PdCSD2OE</i> xylem, indicating an increase in crystalline cellulose content in <i>PdCSD2OE</i> xylem (Figure 1d).</p><p>Lignin is a primary factor that affects cell wall digestibility and saccharification (Halpin, <span>2019</span>). Therefore, this study also aims to establish whether the reduced lignin content in <i>PdCSD2-OE</i> can improve the efficiency of cell wall saccharification. The level of glucose enzymatically released from both untreated and hot 1.5% H<sub>2</sub>SO<sub>4</sub>-pretreated <i>PdCSD2-OE</i> stems was found to be higher compared to WT (Figure 1g). As a parameter of papermaking, fibre length directly affects paper strength and performance, as a greater fibre length enhances paper strength and wear resistance. To assess fibre length changes, the basal stem was disintegrated and fibre cell lengths were measured under a microscope. The fibre cells in the basal stem of <i>PdCSD2-OE</i> were found to be approximately 15% longer than those in WT, with no significant difference observed in fibre cell diameter between <i>PdCSD2-OE</i> and WT (Figure 1h,i). These results suggest the possibility to engineer poplars by overexpressing <i>PdCSD2</i> in the bioethanol and papermaking industries.</p><p>The integration of multiple genes for plant transformation provides a novel solution to plant genetic engineering, which allows multiple traits to be modified simultaneously (Naqvi <i>et al</i>., <span>2010</span>). Pests represent a critical factor that constrains forestry production and development. Originating from the bacterium <i>Bacillus thuringiensis</i> (Bt), the poplar expressing insect-specific toxins exert an inhibitory effect on lepidopteran and coleopteran pests. In this study, <i>Cry3A</i> gene is introduced into the <i>PdCSD2OE</i> plants. Two transgenic poplar lines with high Cry3A expression levels and protein toxin content, 3# and 7#, exhibited normal growth but no discernible phenotypic variances compared to <i>PdCSD2OE</i> plants (Figure 1k; Figures S5–S8). Third-instar <i>Plesioclytus versicolora</i> larvae were fed with the leaves derived from WT, <i>PdCSD2OE</i> and <i>PdCSD2/Cry3AOE</i> poplar plants. After 2 days of larval feeding, <i>PdCSD2/Cry3AOE</i> poplar leaves demonstrated stronger resistance than WT and <i>PdCSD2OE</i> plants (Figure 1n). The mortality rate of third-instar <i>P. versicolora</i> larvae feeding on <i>PdCSD2/Cry3AOE</i> poplar leaves was found to be significantly higher than those feeding on WT and <i>PdCSD2OE</i> leaves for both 4 and 8 days (Figure 1m). These results indicate that <i>PdCSD2/Cry3A-OE</i> poplar plants resisted higher toxicity towards <i>P. versicolora</i> larvae while maintaining a similar trend of growth to <i>PdCSD2OE</i> plants. The phenotype of 1-year-old transgenic plants grown in the field was further verified. As shown in Figures S10 and S11, the difference in lignin content and fibre length is consistent with that exhibited by those transgenic plants grown in greenhouses. Compared to the wild type, higher bending strength is exhibited by the stem of <i>PdCSD2OE</i> and <i>PdCSD2/Cry3AOE</i> poplars (Figure S12).</p><p>In summary, <i>PdCSD2</i> overexpression enhances cambium activity, which increases wood production, reduces lignin content, elevates cellulose content and increases fibre cell length. Furthermore, the use of wood derived from <i>PdCSD2OE</i> poplar trees for bioethanol production and papermaking could lower cost, mitigate pollution and improve paper quality. In this study, <i>PdCSD2Cry3AOE</i> poplar trees are developed through multigene transformation. They exhibit not only an improvement in biomass and wood quality relative to <i>PdCSD2OE</i> poplar trees, but also a better performance in pest resistance. This strategy is expected to be applicable in practice.</p><p>The authors declare no conflict of interest.</p><p>DW, CW and GZ designed the experiments; DW, FL, MZ, XY, JF and WW performed the experiments. DW wrote the manuscript. ML, WL, XT, CW and GZ revised the manuscript. All authors read and approved the manuscript.</p>","PeriodicalId":221,"journal":{"name":"Plant Biotechnology Journal","volume":"23 4","pages":"1345-1347"},"PeriodicalIF":10.5000,"publicationDate":"2025-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/pbi.14590","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Biotechnology Journal","FirstCategoryId":"5","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/pbi.14590","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
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Abstract

Wood, one of the most abundant renewable natural resources globally, plays a crucial role in the timber, papermaking and bioenergy industries (Chutturi et al., 2023). Wood (i.e. secondary xylem) is derived from vascular cambium, which is pivotal in determining the wood biomass in woody plants (Tang et al., 2022). Reactive oxygen species (ROS) act as signalling molecules that regulate plant development, growth and responses to abiotic and biotic stresses (Wang et al., 2024). Numerous studies underscore the significance of ROS in maintaining the root and shoot stem cell niches (Wang et al., 2024). A recent study has indicated that LATERAL ORGAN BOUNDARIES DOMAIN 11 (LBD11) governs several ROS metabolic genes to manage the specific distribution of ROS within the cambium, thus affecting cambial cell proliferation in Arabidopsis root and shoot (Dang et al., 2023). However, there remains a lack of clarity on the biological functions of ROS accumulation in tree vascular cambium activity. Additionally, the localized accumulation of ROS is required for lignin biosynthesis (Wang et al., 2024). Therefore, ROS homeostasis enables woody plants to fine-tune the activity of cambium, increase wood yield and improve their quality.

In plants, various forms of ROS exist, including singlet oxygen (1O2), superoxide anion (O2·−), hydrogen peroxide (H2O2), hydroxyl radical (HO·) and others. Among them, O2·− and H2O2 play a crucial role in regulating stem cell fate in shoot apical meristem (SAM) and root apical meristem (RAM) (Wang et al., 2024). Superoxide dismutases (SODs) are a group of metalloenzymes that scavenge ROS by converting O2·− radicals into H2O2. In SAM and RAM, the balance between O2·− and H2O2 plays a critical role in the maintenance and differentiation of stem cells (Zeng et al., 2017). Since the development of vascular cambium originates from the peripheral region of SAM, the balance between O2·− and H2O2 may also contribute significantly to vascular cambium activity. In this study, 11 SOD genes were identified in Populus genome (Figure S1). As revealed by the cell-type transcriptome analysis of the poplar stem (Dai et al., 2023), among the 11 SOD genes, CSD2 has a higher specific expression level in the cambium other than in the xylem or phloem, indicating a potential role of CSD2 in vascular cambium development (Figure 1a).

To assess the effect of PdCSD2 on wood formation, the PdCSD2 overexpression (OE) lines with substantially elevated PdCSD2 transcript levels were developed in this study (Figure S2). Compared to the wild type (WT), the PdCSD2-OE lines exhibited a significant enhancement of growth with about a 10% increase in height and about a 20% increase in stem diameter (Figure 1b; Figure S3). Analysis of stem cross-sections revealed a 30% rise in the number of cambium cell layers at the 20th internode of PdCSD2OE plants in comparison to WT (Figure 1c; Figure S4). Accordingly, the xylem width at the 20th internode in PdCSD2OE plants was increased by approximately 20% relative to WT. Therefore, PdCSD2OE significantly enhances the wood biomass (Figure 1c; Figure S4). Numerous studies have demonstrated the essential role of ROS in regulating secondary cell wall formation, including lignin and cellulose biosynthesis and deposition (Dang et al., 2023; Wang et al., 2024). The overexpression of the SOD enzyme encoding gene PdCSD2 is suspected to affect ROS accumulation and thus lignin content in xylem. To investigate the effect of PdCSD2 on lignin biosynthesis and xylem cell wall lignification, the xylem of the 20th internode of poplar was stained with phloroglucinol–HCl solution. A diminished staining intensity was observed in PdCSD2-OE plants compared to WT, as discovered for the growth of 1-year-old transgenic plants in fields (Figure 1d; Figure S11). Accordingly, the lignin content in the 20th internodes was reduced by 15% compared to that of WT (Figure 1e). These results provide evidence supporting the association between ROS and lignin biosynthesis. To investigate the effect of ROS on cellulose biosynthesis, pontamine fast scarlet 4B (S4B) staining was conducted on xylem sections of PdCSD2OE and WT plants. An increased staining intensity in PdCSD2OE xylem was observed, indicating elevated cellulose levels (Figure 1d). Furthermore, quantification of cellulose content revealed at least 15% higher cellulose content in PdCSD2OE plants compared to WT (Figure 1f). To evaluate the potential differences in the crystalline cellulose content of PdCSD2OE xylem, whole-mount immunolabelling assays were performed on the xylem section using a family 3 carbohydrate-binding module (CBM3a) antibody that specifically targets crystalline cellulose. The fluorescence intensity was found to be significantly enhanced in the sections of PdCSD2OE xylem, indicating an increase in crystalline cellulose content in PdCSD2OE xylem (Figure 1d).

Lignin is a primary factor that affects cell wall digestibility and saccharification (Halpin, 2019). Therefore, this study also aims to establish whether the reduced lignin content in PdCSD2-OE can improve the efficiency of cell wall saccharification. The level of glucose enzymatically released from both untreated and hot 1.5% H2SO4-pretreated PdCSD2-OE stems was found to be higher compared to WT (Figure 1g). As a parameter of papermaking, fibre length directly affects paper strength and performance, as a greater fibre length enhances paper strength and wear resistance. To assess fibre length changes, the basal stem was disintegrated and fibre cell lengths were measured under a microscope. The fibre cells in the basal stem of PdCSD2-OE were found to be approximately 15% longer than those in WT, with no significant difference observed in fibre cell diameter between PdCSD2-OE and WT (Figure 1h,i). These results suggest the possibility to engineer poplars by overexpressing PdCSD2 in the bioethanol and papermaking industries.

The integration of multiple genes for plant transformation provides a novel solution to plant genetic engineering, which allows multiple traits to be modified simultaneously (Naqvi et al., 2010). Pests represent a critical factor that constrains forestry production and development. Originating from the bacterium Bacillus thuringiensis (Bt), the poplar expressing insect-specific toxins exert an inhibitory effect on lepidopteran and coleopteran pests. In this study, Cry3A gene is introduced into the PdCSD2OE plants. Two transgenic poplar lines with high Cry3A expression levels and protein toxin content, 3# and 7#, exhibited normal growth but no discernible phenotypic variances compared to PdCSD2OE plants (Figure 1k; Figures S5–S8). Third-instar Plesioclytus versicolora larvae were fed with the leaves derived from WT, PdCSD2OE and PdCSD2/Cry3AOE poplar plants. After 2 days of larval feeding, PdCSD2/Cry3AOE poplar leaves demonstrated stronger resistance than WT and PdCSD2OE plants (Figure 1n). The mortality rate of third-instar P. versicolora larvae feeding on PdCSD2/Cry3AOE poplar leaves was found to be significantly higher than those feeding on WT and PdCSD2OE leaves for both 4 and 8 days (Figure 1m). These results indicate that PdCSD2/Cry3A-OE poplar plants resisted higher toxicity towards P. versicolora larvae while maintaining a similar trend of growth to PdCSD2OE plants. The phenotype of 1-year-old transgenic plants grown in the field was further verified. As shown in Figures S10 and S11, the difference in lignin content and fibre length is consistent with that exhibited by those transgenic plants grown in greenhouses. Compared to the wild type, higher bending strength is exhibited by the stem of PdCSD2OE and PdCSD2/Cry3AOE poplars (Figure S12).

In summary, PdCSD2 overexpression enhances cambium activity, which increases wood production, reduces lignin content, elevates cellulose content and increases fibre cell length. Furthermore, the use of wood derived from PdCSD2OE poplar trees for bioethanol production and papermaking could lower cost, mitigate pollution and improve paper quality. In this study, PdCSD2Cry3AOE poplar trees are developed through multigene transformation. They exhibit not only an improvement in biomass and wood quality relative to PdCSD2OE poplar trees, but also a better performance in pest resistance. This strategy is expected to be applicable in practice.

The authors declare no conflict of interest.

DW, CW and GZ designed the experiments; DW, FL, MZ, XY, JF and WW performed the experiments. DW wrote the manuscript. ML, WL, XT, CW and GZ revised the manuscript. All authors read and approved the manuscript.

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通过双基因表达工程改造杨树,提高生物量、木材品质和抗虫害能力
木材是全球最丰富的可再生自然资源之一,在木材、造纸和生物能源行业中发挥着至关重要的作用(Chutturi et al., 2023)。木材(即次生木质部)来源于维管形成层,这是木本植物木材生物量的关键决定因素(Tang et al., 2022)。活性氧(ROS)作为信号分子调节植物的发育、生长和对非生物和生物胁迫的响应(Wang et al., 2024)。大量研究强调了ROS在维持根冠干细胞生态位中的重要性(Wang et al., 2024)。最近的一项研究表明,LATERAL ORGAN BOUNDARIES DOMAIN 11 (LBD11)调控多个ROS代谢基因来管理ROS在形成层内的特定分布,从而影响拟南芥根和茎形成层细胞的增殖(Dang et al., 2023)。然而,活性氧积累在树维管形成层活性中的生物学功能尚不清楚。此外,木质素的生物合成需要ROS的局部积累(Wang et al., 2024)。因此,活性氧的动态平衡可以使木本植物对形成层的活性进行微调,从而提高木材产量和品质。植物体内存在多种形式的活性氧,包括单线态氧(1O2)、超氧阴离子(O2·−)、过氧化氢(H2O2)、羟基自由基(HO·)等。其中,O2·−和H2O2在茎尖分生组织(SAM)和根尖分生组织(RAM)的干细胞命运调控中起着至关重要的作用(Wang et al., 2024)。超氧化物歧化酶(sod)是一类通过将O2·−自由基转化为H2O2来清除活性氧的金属酶。在SAM和RAM中,O2·−和H2O2之间的平衡在干细胞的维持和分化中起着关键作用(Zeng et al., 2017)。由于维管形成层的发育起源于SAM的外周区域,因此O2·−和H2O2之间的平衡也可能对维管形成层的活性起重要作用。本研究在杨树基因组中鉴定出11个SOD基因(图S1)。通过对杨树茎的细胞型转录组分析(Dai et al., 2023)发现,在11个SOD基因中,CSD2在形成层中的特异性表达水平高于木质部或韧皮部,这表明CSD2在维管形成层发育中可能发挥作用(图1a)。图1在powerpoint视图中打开工程转基因杨树,生物量、木材品质和抗虫害能力增强。(a)杨树茎形成层、木质部和韧皮部细胞中SOD编码基因家族转录丰度,采用LCM采集杨树茎第8节间细胞进行RNA-seq分析。(b) 3月龄PdCSD2过表达(PdCSD2OE)转基因植株的表型。杆,10厘米。(c) 3月龄WT和PdCSD2OE转基因植株第20个节间茎横切面和甲苯胺蓝染色(中)。WT和PdCSD2OE植物形成层细胞(左)和次生木质部(右)的详细观察。棒材,25 μm(右);100 μm(中);25 μm(右)。(d) 3月龄WT和PdCSD2OE转基因植株第20个节间茎细胞壁间苯三酚- hcl(左)和木质素含量(e)的组织化学染色。用S4B反染色(中),用CBM3a抗体(右)和3月龄WT和PdCSD2OE转基因植株第20个节间茎细胞壁的纤维素含量(f)对结晶纤维素进行全株免疫标记。棒材,25 μm(右);50 μm(中、右)。数据代表每条线上至少6个工厂的平均值±SD。(g)预处理或不预处理WT和PdCSD2OE转基因植物的干细胞壁材料的糖化。数据代表每条线上至少六个工厂的平均值±SD。(h) 3月龄植物基部节间纤维细胞水解,TBO染色。bar = 50 μm。(i, j) WT和PdCSD2OE之间的纤维细胞长度和宽度。随机选取每系60多个纤维细胞进行测量。(k) 3月龄PdCSD2和Cry3A过表达(PdCSD2/Cry3AOE)转基因植株的表型。杆,10厘米。(l) PdCSD2/Cry3AOE系(1#和7#)幼叶Cry3A蛋白检测。数据代表每条线上至少三个工厂的平均值±SD。(m)以WT、PdCSD2OE和PdCSD2/Cry3AOE叶片为食的三龄花斑拟合虫的死亡率数据。数据为每系三个生物重复的平均值±SD。(n) WT、PdCSD2OE和PdCSD2/Cry3AOE给药2天后叶片的比较。统计学差异采用Duncan检验,不同字母表示P &lt; 0.05显著差异。为了评估PdCSD2对木材形成的影响,本研究开发了PdCSD2过表达(OE)系,这些系的PdCSD2转录水平大幅提高(图S2)。 与野生型(WT)相比,PdCSD2-OE系表现出显著的生长增强,高增加了约10%,茎粗增加了约20%(图1b;图S3)。茎截面分析显示,与WT相比,PdCSD2OE植株第20节间形成层细胞层数增加了30%(图1c;图S4)。与WT相比,PdCSD2OE植株第20节间木质部宽度增加了约20%。因此,PdCSD2OE显著提高了木材生物量(图1c;图S4)。大量研究表明,活性氧在调节次生细胞壁形成,包括木质素和纤维素的生物合成和沉积中发挥重要作用(Dang et al., 2023;Wang等人,2024)。SOD酶编码基因PdCSD2的过表达被怀疑影响ROS的积累,从而影响木质部的木质素含量。为了研究PdCSD2对木质素生物合成和木质部细胞壁木质化的影响,采用间苯三酚-盐酸对杨树第20节间木质部进行了染色。与WT相比,PdCSD2-OE植株的染色强度降低,这是在田间生长1年的转基因植株中发现的(图1d;图S11)。与WT相比,第20节间木质素含量降低了15%(图1e)。这些结果为活性氧与木质素生物合成之间的联系提供了证据。为了研究活性氧对纤维素生物合成的影响,对PdCSD2OE和WT植株木质部切片进行了波胺耐晒红4B (S4B)染色。观察到PdCSD2OE木质部染色强度增加,表明纤维素水平升高(图1d)。此外,纤维素含量的定量分析显示,与WT相比,PdCSD2OE植株的纤维素含量至少高出15%(图1f)。为了评估PdCSD2OE木质部中结晶纤维素含量的潜在差异,使用专门针对结晶纤维素的3族碳水化合物结合模块(CBM3a)抗体对木质部切片进行了全挂免疫标记试验。PdCSD2OE木质部切片的荧光强度明显增强,表明PdCSD2OE木质部中结晶纤维素含量增加(图1d)。木质素是影响细胞壁消化率和糖化的主要因素(Halpin, 2019)。因此,本研究还旨在确定PdCSD2-OE中木质素含量的降低是否可以提高细胞壁糖化效率。与WT相比,未经处理和1.5% h2so4预处理的PdCSD2-OE茎中酶促释放的葡萄糖水平更高(图1g)。纤维长度作为造纸的一个参数,直接影响纸张的强度和性能,纤维长度越大,纸张的强度和耐磨性就越高。为了评估纤维长度的变化,在显微镜下分解基茎并测量纤维细胞的长度。发现PdCSD2-OE的基茎纤维细胞比WT长约15%,但PdCSD2-OE和WT的纤维细胞直径没有显著差异(图1,1)。这些结果表明,通过在生物乙醇和造纸工业中过表达PdCSD2来改造杨树的可能性。多基因整合植物转化为植物基因工程提供了一种新的解决方案,可以同时修改多个性状(Naqvi et al., 2010)。有害生物是制约林业生产和发展的一个关键因素。源自苏云金芽孢杆菌(Bacillus thuringiensis, Bt)的杨树表达昆虫特异性毒素,对鳞翅目和鞘翅目害虫具有抑制作用。本研究将Cry3A基因导入PdCSD2OE植株。Cry3A高表达和蛋白毒素含量的2个转基因杨树品系3#和7#与PdCSD2OE植株相比生长正常,但没有明显的表型差异(图1k;图S5-S8)。以WT、PdCSD2OE和PdCSD2/Cry3AOE杨树叶片为食,饲喂三龄花青树幼体。幼虫摄食2天后,PdCSD2/Cry3AOE杨树叶片的抗性强于WT和PdCSD2OE植株(图1n)。结果发现,以PdCSD2/Cry3AOE杨树叶片为食的三龄花斑小蠊幼虫4天和8天的死亡率均显著高于以WT和PdCSD2OE叶片为食的三龄幼虫(图1m)。这些结果表明,PdCSD2/Cry3A-OE杨树植株在保持与PdCSD2OE植株相似的生长趋势的同时,对花斑纸虱幼虫具有更高的毒力。进一步验证了田间1年生转基因植株的表型。 如图S10和S11所示,木质素含量和纤维长度的差异与温室中转基因植株的差异一致。与野生型相比,PdCSD2OE和PdCSD2/Cry3AOE杨树茎秆的抗弯强度更高(图S12)。综上所述,PdCSD2过表达可增强形成层活性,从而增加木材产量,降低木质素含量,提高纤维素含量,增加纤维细胞长度。此外,利用PdCSD2OE杨树的木材生产生物乙醇和造纸可以降低成本,减轻污染,提高纸张质量。本研究通过多基因转化培育出PdCSD2Cry3AOE杨树。与PdCSD2OE杨树相比,它们不仅在生物量和木材质量上有提高,而且在抗虫害方面也有更好的表现。这一战略可望在实践中适用。
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来源期刊
Plant Biotechnology Journal
Plant Biotechnology Journal 生物-生物工程与应用微生物
CiteScore
20.50
自引率
2.90%
发文量
201
审稿时长
1 months
期刊介绍: Plant Biotechnology Journal aspires to publish original research and insightful reviews of high impact, authored by prominent researchers in applied plant science. The journal places a special emphasis on molecular plant sciences and their practical applications through plant biotechnology. Our goal is to establish a platform for showcasing significant advances in the field, encompassing curiosity-driven studies with potential applications, strategic research in plant biotechnology, scientific analysis of crucial issues for the beneficial utilization of plant sciences, and assessments of the performance of plant biotechnology products in practical applications.
期刊最新文献
DcH3.3 and DcNAC1 Regulate the Expression of UGT73A93 Involved in the Changes in Flower Colour and Fungal Resistance in Carnation Engineering of Amygdalin Biosynthesis in Rice Endosperm for Pharmaceutical Production and Sitophilus oryzae Resistance Mapping and Functional Characterization of Homologous Genes AhSUCA06 and AhSUCA16 Underlying Sucrose, Oil and Protein Contents in Peanut (Arachis hypogaea L.). Transcriptional Regulation of the Novel Theacrine Synthase Gene CsTcS2 by the CsTINY-CsWRKY33 Module Underpins Theacrine Biosynthesis in Camellia sinensis. Unfolding Plant Defence: Endoplasmic Reticulum Stress Signalling at the Plant‐Pathogen Interface
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