The 636-bp-long cDNA sequence of OsCu/Zn-SOD (AK059841) was cloned from Oryza sativa var. Longjing11 via reverse transcription polymerase chain reaction (RT-PCR). The encoded protein comprised of 211 amino acids is highly homologous to Cu/Zn-SOD proteins from tuscacera rice and millet. Quantitative RT-PCR revealed that in rice, the level of OsCu/Zn-SOD gene expression was lowest in roots and was highest in petals and during the S5 leaf stage. Moreover, the expression level of OsCu/Zn-SOD gene expression decreased during the L5 leaf stage to maturity. The level of OsCu/Zn-SOD gene expression, however, was increased under saline–sodic stress and NaHCO3 stress. Germination tests under 125, 150, and 175 mM NaCl revealed that OsCu/Zn-SOD-overexpressing lines performed better than the non-transgenic (NT) Longjing11 lines in terms of germination rate and height. Subjecting seedlings to NaHCO3 and water stress revealed that OsCu/Zn-SOD-overexpressing lines performed better than NT in terms of SOD activity, fresh weight, root length, and height. Under simulated NaHCO3 stress, OsCu/Zn-SOD-overexpressing lines performed better than NT in terms of survival rate (25.19% > 6.67%) and yield traits (average grain weight 20.6 > 18.15 g). This study showed that OsCu/Zn-SOD gene overexpression increases the detoxification capacity of reactive oxygen species in O. sativa and reduces salt-induced oxidative damage. We also revealed the regulatory mechanism of OsCu/Zn-SOD enzyme in saline–sodic stress resistance in O. sativa. Moreover, we provided an experimental foundation for studying the mechanism of OsCu/Zn-SOD enzymes in the chloroplast.

Citation: Guan Q, Liao X, He M, Li X, Wang Z, Ma H, et al. (2017) Tolerance analysis of chloroplast OsCu/Zn-SOD overexpressing rice under NaCl and NaHCO3 stress. PLoS ONE 12(10): e0186052. https://doi.org/10.1371/journal.pone.0186052

Editor: Jin-Song Zhang, Institute of Genetics and Developmental Biology Chinese Academy of Sciences, CHINA

Received: April 6, 2017; Accepted: September 25, 2017; Published: October 11, 2017

Copyright: © 2017 Guan et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Data Availability: All expression profiles files are available from the NCBI database (accession numbers: AK059841).

Funding: This work was supported by the Fundamental Research Funds for the Central Universities (Grant no. 2572016EAJ6); The National Key Research and Development Program of China (2016YFC0501203); The Heilongjiang Postdoctoral Scientific Research Developmental Fund (LBH408 Q15004) and the Program for Chang jiang Scholars and Innovative Research Team in University (IRT13053).

Competing interests: The authors have declared that no competing interests exist.

Abbreviations: APX, ascorbic acid peroxidase; CAT, catalase; CaMV, Cauliflower mosaic virus; GFP, green fluorescent protein; GR, glutathione reductase; LJ11, LongJing11; MDA, Malondialdehyde; MS, Murashige and Skoog; NT, Non-transgenic rice; POD, peroxidase; ROS, reactive oxygen species; SOD, superoxide dismutase; WT, Wild type

Plants adapt to various environmental conditions by actively regulating their internal metabolism. The enzyme superoxide dismutase (SOD, EC 1.15.1.1) determines the reaction rate in any metabolic pathway in plants. SOD is the most important enzyme that responds to reactive oxygen species (ROS) and is specifically produced by the biological PSI–PSП system. SOD catalyzes the superoxide anion, a free radical, into H2O2 [1]. Generally, the tolerance to oxidative stress is an important factor that affects lifespan, and the activity of ROS-scavenging enzymes is particularly important [2; 3; 4]. When the metabolic cycle of plant cells is disrupted, the activity of Cu/Zn-SOD enzymes is directly affected and superoxide anion radicals accumulate, thus causing oxidative stress [5]. Meanwhile, SOD is the first enzyme to clear active oxygen-free radicals, SOD activity level is associated with oxidation resistance and lifespan [6]. Hitherto, molecular biology, structural biology, and bioinformatics techniques have been used to investigate the factors that affect SOD activity at the sequence and structure level [7; 8; 9]. Some studies have shown that C24H26O5 enhances SOD activity, which signifying increased plant responses against damage [10]. The addition of exogenous proline and glycine betaine enhances the antioxidant defense system of Oryza sativa, the SOD activity of glyoxalase systems, and the resistance to salt-induced oxidative stress [11].

To improve genetic resources, genetic engineering has been performed by scientific workers in various countries and the study of transgenic plants has expanded. The SOD gene has been cloned from many plant species. Transgenic tobacco with the rice (Oryza sativa) chloroplast SOD gene has salt, water, and PEG stress tolerance; moreover, the tobacco chloroplast antioxidant system has been optimized [12]. Transgenic wheat protoplasts with the tobacco Mn-SOD gene showed lower levels of oxidative damage and higher levels of SOD and GR activities [13]. Transgenic Populus L. that overexpression of the Tamarix androssowii Mn-SOD gene has enhanced salt tolerance as a result of SOD activity being increased; furthermore, the relative biomass of the transgenic plants increased by 8- to 23-fold [14]. Put Cu/Zn-SOD-overexpressing Arabidopsis thaliana has enhanced resistance to saline–sodic stress and growth tolerance to H2O2 stress [15]. In Mn-SOD-overexpressing A. thaliana shows that the tolerance to NaCl stress was increased and the levels of Mn-SOD, Cu/Zn-SOD, Fe-SOD, CAT, and POD expression also have been improved under salt stress [16]. The overexpression of tobacco Mn-SOD/APX in transgenic tall fescue plant confers increased tolerance to MV, H2O2, Cu, Cd, and as stresses as a result of SOD and APX enzyme activities being increased [17]. The increase of SOD, CAT, GR and APX activities enhances tolerance to sulfur dioxide (SO2) stress in transgenic Chinese cabbage plants that overexpress the A. thaliana Mn-SOD/CAT gene [18]. The overexpression of Mn-SOD (Nicotiana plumbaginifolia) + Fe-SOD (A. thaliana) in transgenic alfalfa enhances resistance against drought stress and improves photosynthetic efficiency [19]. The overexpression of cytosolic copper/zinc superoxide dismutase (Cu/Zn-SOD) from the mangrove plant Avicennia marina in indica rice var Pusa Basmati enhances tolerance to oxidative, salt, and drought stresses [20]. Saline-sodic stress is caused by salt and pH variation. The in vivo accumulation of ROS injures cell membranes via lipid oxidation, and the accumulation of a large amount of membrane lipid peroxidation products, such as MDA is a cause or product of membrane lipid peroxidation, and also is one of the most obvious indicators of oxidative stress [21; 22]. So far, there have been few reports on the regulatory effects of CuZn-SOD overexpression on saline–sodic stress tolerance in rice.

In this study, we cloned the chloroplast OsCu/Zn-SOD gene in O.sativa Long jing11, which belongs to one of the eight SOD genes identified in rice including 5 Cu/ZnSODs, 2 FeSODs, and 1 MnSOD[23]. We performed subcellular localization analysis to verify that OsCu/Zn-SOD localized in the chloroplast. Then, we compared the resistance of transgenic rice to NaCl stress with that of non-transgenic (NT) rice during germination and the tolerance of transgenic rice to sodic salt (NaHCO3) stress with that of NT rice during the seedling stage of growth. We compared the physiological indexes of OsCu/Zn-SOD-overexpressing transgenic with NT rice lines under NaHCO3 stress during vegetative growth. We simulated the effects of OsCu/Zn-SOD gene overexpression on seed-setting in rice under sodic salt stress. Our study provides the experimental foundation for analyzing the protective mechanism of chloroplast Cu/Zn-SOD in salt–sodic-induced oxidative stress and for novel rice cultivars with tolerance for saline–sodic stress.

Seeds of O. sativa L. var. Longjing11 were maintained at Northeast Agricultural University. We selected a white Allium cepa variety and an A. thaliana ecotype. Columbia seeds were maintained and propagated in sodic soil at the Natural Environmental Research Center of Northeast Forestry University.

Escherichia coli JM109 and Agrobacterium tumefaciens EHA105 were maintained in our laboratory. The pMD18-T vector was procured from TaKaRa Company. The pCXSN and pBI121-MCS-GFP botanical expression vectors were maintained saved in our laboratory.

Various restriction enzymes, T4-DNA ligase, and gel recovery reagents were obtained from Fermentas. Ex-Taq DNA polymerase and reverse transcription kits were purchased from Invitrogen. Real-time quantitative fluorescent dyes and SYBR Green QPCR Master Mix were purchased from Toyobo (Japan). Northern blot kits were purchased from Roche. Antibiotics were purchased from Sigma-Aldrich. All other analytical reagents were made in China.

Premier 5.0 software was used to design RT-PCR primers based on the nucleotide sequence for Cu/Zn-SOD of rice (AK059841, LOC_Os08g44770 OsCu/Zn-SOD,) that were retrieved from the GenBank gene registry. Takara Ex-Taq high fidelity enzyme was used to synthesize the following primer sequences: OsCu/Zn-SOD-P1 F1: 5’-tatcatcgtcaggtcaggca-3’; OsCu/Zn-SOD-R1: 5’-acacttcagctgcaacttgc-3’. Total RNA was extracted from seedling leaves (four leaves and a bud) for the reverse transcription of the cDNA template. The OsCu/Zn-SOD gene fragment was amplified and cloned via PCR.

PCR conditions consisted of pre-denaturation at 95°C for 5min; followed by 35 cycles of: 95°C for 30 s, 55°C for 30 s, 72°C for 45s, and and an extension of 72°C for 10 min. The PCR products were resolved by 1% agarose gel electrophoresis. After the target DNA fragment was then retrieved, they were linked with pMD18-T vector. Subsequently, they were transformed to JM109, and then sent to Beijing Genomics Institute (BGI) for restriction enzyme digestion.

To identify the subcellular localization of OsCu/Zn-SOD protein, Kpn I and Spe I were added to the 5′ and 3′ ends, respectively, of the OsCu/Zn-SOD open reading frame (ORF). The primer OsCu/Zn-SOD-P2 was then designed with the following sequences: F2: 5′-cttggtacc atgcaagccatcctcgcc-3′; OsCu/Zn-SOD-R2: 5′-catactagtcaacggggtcagcccaa caac-3′. The primers were synthesized by Shanghai Biological Company. The 1% plasmid of pMD18-T::OsCu/Zn-SOD was used as the PCR template. The pBI121-OsCu/Zn-SOD::GFP expression vector was constructed via enzyme digestion, ligation, and transformation.

To construct the overexpressing vector initiated by the 35S promoter, we amplified OsCu/Zn-SOD gene via PCR with the following primers: OsCu/Zn-SOD P3 F2: 5′-cttggtaccatgcaagccatcctcgcc-3′; OsCu/Zn-SOD-R1: 5′-acacttcagctgcaac ttgc-3′. The products were then ligated and then transformed into pCXSN-T. After restriction digestion with Xcm I., it shows the identification and construction of pCXSN::OsCu/Zn-SOD 2D plant expression vector. The vector was then transformed into Agrobacterium EHA105 via electric shock transformation. PCR was used to detect successful transformants.

Tissue samples were collected from Longjing 11 plants that were pot-cultured in a greenhouse. The tissue samples were frozen in liquid nitrogen at −80°C. To simulate salt and sodic stress, plants were cultured in Hough nutrient solution with 150 mM NaCl and 60 mM NaHCO3 for 2, 4, 8, 16, and 24 h. Water was used as the control treatment (0 h stress time). Three leaves and a bud were harvested from each plant. Roots and leaves were also collected and frozen in liquid nitrogen at −80°C.

Total RNA was extracted via Trizol one-step method. First, 1 μg of total RNA template was reverse-transcribed into cDNA and then diluted ten-fold for quantitative PCR. OsCu/Zn-SOD gene transcripts were identified via quantitative RT-PCR (qRT-PCR) with the following specific primers for OsCu/Zn-SOD-RT-P4: qRT-F: 5′-tatcatcgtcaggtcaggca-3′; qRT-R: 5′-acacttcagctgcaacttgc-3′, Amplification was conducted with the following protocol: 95°C for 5min; followed by 40 cycles of: 95°C for 30 s, 55°C for 30 s, and 72°C for 30 s. PCR was conducted with 2× Brilliant III SYBR Green QPCR Master Mix (Agilent). Data were acquired on the MxPro-Mx3000P system. All gene expression levels were normalized to that of the internal reference actin1 gene (Actin1-F: 5′-cttcatag gaatggaagct gcgggta-3′; Actin1-R: 5′-cgacca ccttgatcttcatgctgcta-3′). No template control (NTC) was set at the same time. Each reaction was repeated thrice. After PCR, relative gene expression was calculated by the system based on the relative quantitative method with the following formula: Rel Exp = 2−ΔΔCt, where ΔCt = Ct(OsCu/Zn-SOD) − Ct(Actin1); ΔΔCt = (Under stress treatment ΔCt) − (Not under treatment ΔCt). A chart was generated based on fold changes in expression. Excel format was used for the output.

pBI121-OsCu/Zn-SOD::GFP and the chloroplast marker mcherry were transformed into epidermal cells of onion via particle bombardment [24]. Then the onion epidermal cells were placed onto a tablet and the transformants were incubated for 18–24 h. The GFP fluorescence was observed under a confocal microscope (Olympus).

A. thaliana inflorescence was transformed via infection with Agrobacterium EHA105 containing pBI121-OsCu/Zn-SOD::GFP plasmid DNA using 50 mg/L of T0 Kana screen seed. The T1 generation of Kana-resistant positive lines was detected via PCR (OsCu/Zn-SOD-F2/R2) using Tape-Arabidopsis Sandwich extract A. thaliana leaf T1 protoplast cells [25]. The GFP fluorescence was observed under a confocal microscope (Olympus).

Longjing 11 was genetically transformed with the 35S::OsCu/Zn-SOD construct. After rice Longjing 11 seeds were sterilized, 2 mg/L 2, 4-dichlorophenoxyacetic acid was added to the culture medium for callus induction. The calluses were cultured in an illuminated incubator at 30°C for 3 weeks. Naturally split embryogenic calluses were screened on a clean workbench with tweezers. The selected calluses were then co-cultured after 1 week. Agrobacterium was treated with electroporation. Then, pCXSN::OsCu/Zn-SOD plasmid DNA monoclone was placed into 4 ml YEP culture medium with 50 mg/L Kana and 0 mg/L Hyg and then shaking culture at 28°C and 250 rpm for approximately 20–36 h until reaching an ODλ = 600 of approximately 0.5. The culture supplemented with acetosyringone (AS, its final concentration is 100 m mol/L) were used to infect the calluses [26, 27].

After screening, differentiation, rooting, and germination with Hyg, T0 generation transgenic plants were obtained and T1 seeds were harvested. After the seeds from NT and T1-#1, #2, #3, #4, and #5 transgenic lines being screened, they were used for Germination tests. Seeds were disinfected with 3% H2O2 for 30 min and then washed with distilled water. Germination was accelerated by treating seeds with 50 mg/L Hyg aqueous solution at 30°C. After nine–day germination, seedlings with vigorous radicle and plumule were selected for transplantation. To test primer specificity (F2, 5′-ctt ggtaccatgcaagccatcctcgcc-3′, NOS-R, 5′-atcggggaaattcgctagtg-3′) and the genomic condition of the transgenic lines T1-#1, #2, #3, #4, #5, genomic DNA was extracted from the leaves of transgenic Cu/Zn-SOD lines via CTAB method [28].

Total RNA was extracted from transgenic, NT, and T3-#1, #2, #3 lines via Trizol one-step method and the 5 μg of the total sample was used for denaturation at 65°C for 10 min. After separation by the 1.5% formaldehyde-agarose gel and then the sample was transferred to the Hybond-N+ cellulose nitrate membrane. RNA was cross-linked to the membrane using ultraviolet irradiation. The membrane was crossed by DIG—chloroplast precursor OsCu/Zn-SOD (AK059841) DNA specific probes at 50°C for 12 h using CDP-StarTM reagent (Roche company). Signals were detected using LAS 4000 imaging analyzer [29].

NT and T3-#1, #2, #3 seeds were disinfected with 3% H2O2 for 30 min. The seeds were first cultivated at 30°C to investigate resistance to 0, 125, 150, 175 mM NaCl stress during germination. Germination rate, fresh weight, plant height, and MDA content were determined after 7 days. MDA content under stress treatment was determined via thiobarbituric acid-reactive-substance assay [30].

The growth characteristics of NT and T3-#1, #2, #3 under NaHCO3 stress were detected. Germination was accelerated at 30°C in an incubator for 5 days. The uniform-sized seedlings were transferred to Hough stress treatment solutions with 0, 5, 7.5, 10 m mol/L NaHCO3 (each treatment replicated three times). Plants were grown in a culture room at 28°C. The nutrient solution was replaced once every 2 days to its original volume. Growth characteristics, plant height, fresh weight, SOD activity, and chlorophyll changes were investigated after 21 days. NBT staining detected the content of superoxide anion in three leaves from seedlings after stress treatment.

NT and T3-#1, #2, #3 seeds were planted in pots to simulate saline–sodic stress in a field experiment during spring. Field soil and saline–sodic soil patches were obtained from Songneng. Plain and mixed in a basin at ratios of 1:0, 2:1, and 1:1. Groundwater was used for irrigation. Each pot contained three transgenic or NT plants. Ten pots were used for per treatment. The transplant survival rate after 1 month was investigated and plant characteristics under treatment were detected.

A 726-bp-long target gene fragment was cloned via RT-PCR. The cloned fragment was then sent to BGI for sequencing via restriction enzyme digestion. As expected, the cloned nucleotide sequence was identical to OsCu/Zn-SOD (AK059841). The sequences included an ORF that was 636 bp in length and that encoded 211 amino acids. Sequence alignment revealed that Cu/Zn-SOD protein sequences from different species, such as sorghum, wheat, wild rice, millet, and A. thaliana, shared 69%–96% homology (Fig 1A). NCBI analysis showed that the sequences contained one Cu2+ (His-103,105,120,177) and Zn2+ (His-120,128,137,140) binding site and SOD active domain (His-103105120137140177). The cluster analysis and phylogenetic tree of OsCu/Zn-SOD protein and 12 other Cu/Zn-SOD proteins revealed that Cu/Zn-SOD proteins from Longjing 11 rice, wild rice, and millet clustered in the same branch, thus indicating that these three proteins shared the closest evolutionary relationship (Fig 1B).

(A) Highly homologous regions in the amino acid sequences of OsCu/Zn-SOD from different species. The black triangle stands for active site. (B) Phylogenetic tree of OsCu/Zn-SOD generated via NJ method.

https://doi.org/10.1371/journal.pone.0186052.g001

The specific expression of the OsCu/Zn-SOD gene in different rice tissues and organs was analyzed via qRT-PCR. Moreover, the level of transcriptional expression under NaCl and NaHCO3 stress was detected. Results showed (Fig 2A) that the level of OsCu/Zn-SOD gene expression was in all stages of rice growth and development, and was lowest in roots and highest in flowers and during S5. However, it decreased during the L5 stage of growth. In addition, the level of OsCu/Zn-SOD gene expression increased significantly with the increasing duration of exposure to NaCl and NaHCO3 stress (Fig 2B and 2C). The level of OsCu/Zn-SOD gene expression in leaves was significantly higher than that in the root. Under NaCl stress, the level of OsCu/Zn-SOD gene expression increased first and then decreased. The maximum peak expression in roots occurred at 8 h of stress. The maximum peak expression in leaves occurred at 16 h of stress. The relative expression under stress was 9.797-fold higher than that in the control. As a whole, the level of OsCu/Zn-SOD gene expression in leaves increased more significantly than in roots. The level of OsCu/Zn-SOD gene expression was significantly induced by NaHCO3 stress. The maximum peak expression in leaves occurred at 8 h of NaHCO3 stress and was 31.362-fold that of the control. The results showed the level of OsCu/Zn-SOD gene expression was significantly higher under NaHCO3 stress than under NaCl stress. ROS were produced during salt–alkali-induced oxidative stress. We speculated that OsCu/Zn-SOD plays a major role in improving the growth of rice when it is subjected to carbonate stress.

(A) Expression patterns of OsCu/Zn-SOD gene in different rice tissues (i.e., root, leaf, tassel, shell, stem, flower, S5, and L5). (B) and (C) OsCu/Zn-SOD expression after treatment with 150 mM NaCl or 60 mM NaHCO3 for 0, 2, 4, 8, 16 and 24 h.

https://doi.org/10.1371/journal.pone.0186052.g002

Onion epidermal cells were co-transformed via particle bombardment. The levels of OsCu/Zn-SOD::GFP fusion green fluorescent protein and mCherry red fluorescent protein expression were observed under confocal microscopy. The subcellular localization of OsCu/Zn-SOD in the chloroplast is shown in Fig 3A. In this image, OsCu/Zn-SOD::GFP fusion protein appears as green fluorescent dots and mcherry appears as red fluorescent dots. PCR detection was used to analyze mesophyll protoplast cells from the T1 generation of Arabidopsis that was integrated with OsCu/Zn-SOD::GFP. Cells were observed under confocal microscopy (Fig 3B). The green fluorescent channel displayed the green fluorescence of GFP. The spontaneous red fluorescence of chloroplasts was also detected via scanning microscopy. The green and red fluorescence overlapped, showing the yellow chloroplast. The results showed that the OsCu/Zn-SOD::GFP fusion protein localized in the chloroplast, thus verifying the subcellular location of OsCu/Zn-SOD in the chloroplast.

(A) To interpret the color references in this figure legend, the reader should refer to the web version of this article. Fluorescence of OsCu/Zn-SOD-GFP fusion protein in onion; merged image of the subcellular localization of the chloroplast marker mcherry; superposition of green fluorescence and mCherry; DIC, bright field. (B) Targeting of GFP fusion proteins to Arabidopsis protoplast. Fluorescence of OsCu/Zn-SOD-GFP fusion protein in a protoplast derived from an Arabidopsis mesophyll cell; autofluorescence of chlorophyll; merged images from green and red channels; protoplast viewed under white light.

https://doi.org/10.1371/journal.pone.0186052.g003

pCXSN::OsCu/Zn-SOD plant expression vector was constructed via T-DNA connection method, as shown in Fig 4A. The callus of Longjing 11 were genetically transformed via Agrobacterium EHA105-mediated infection. T0-generation transgenic lines were obtained and the T1 generation seeds were then harvested. Germination tests were then conducted in 50 mg/L Hyg solution. Although seeds from both NT and T1-#1, #2, #3 were able to germinate, the plumule color and radicle growth of the lines showed drastic differences after 9 days. The plumule of the transgenic lines was green, whereas that of the NT was white. In addition, transgenic lines showed normal radicle growth (S1), whereas NT showed arrested radicle growth. Unlike NT plants, transgenic Cu/Zn-SOD lines (T1-#1, #2, #3) were able to normally grow, develop, and produce seeds. Moreover, the OsCu/Zn-SOD-overexpressing T1-#1, #2, #3, #4, #5 lines are capable of growth in Hyg solution. PCR products were resolved via agarose gel electrophoresis. As shown in Fig 4B, the transgenic lines had 700 bp bands, which is the same as the template plasmid DNA. This result indicated that the 35S::OsCu/Zn-SOD gene was integrated into the genome of the transgenic lines. Northern blot detected the expression of OsCu/Zn-SOD gene in T3-#1, #2, #3. Fig 4C shows the expression of OsCu/Zn-SOD in #1, #2, #3. In this image, the hybrid signal is clear and that the target gene is overexpressed in T3-#1, #2, #3. Therefore, we harvested the seeds from these plants for subsequent experiments.

(A). Schematic of the rice Cu/Zn-SOD gene two-plant expression vector. The vector starts with CaMV35S and is terminated by Tons. The PCXSN::OsCu/Zn-SOD expression vector contains the Hyg resistance gene. (B) PCR detection of the CaMV35S::OsCu/Zn-SOD vector in transgenic Longjing 11, generation T1. CK+- positive plasmid control; NT- nontransgenic Longjing 11. Lanes 1–5 contain PCR products from OsCu/Zn-SOD-overexpressing transgenic Longjing 11 T1 lines. (C) mRNA expression in OsCu/Zn-SOD-overexpressing lines, T3 generation (lanes 1–3) as detected by Northern blot.

https://doi.org/10.1371/journal.pone.0186052.g004

Resistance to NaCl stress during germination NT and OsCu/Zn-SOD (T3-#1, #2) lines showed different seed germination rates after 9 days. Although the root and leaf growth of NT and T3-#1, #2 were the same under water treatment (Fig 5A), those of T3-#1, #2, and #3, were superior to that of NT under 125, 150, 175 mM NaCl treatment. Moreover, although germination rate was inhibited under treatment compared with that under the control, the germination rate of the overexpressing lines was higher than that of NT (Fig 5B). In addition, although leaf growth was inhibited by NaCl stress, the overexpressing lines showed better resistance to NaCl treatment and higher fresh weight than NT (Fig 5C). MDA damage to the cell membrane system occurred as a result of salt and oxidative stress. The MDA content in NT was higher than those in the overexpressing lines. (Fig 5D). NBT staining detected that: (1) there was no difference in the color of 5-day rice seedlings of NT and T3 (#1, #2, #3) which germinated under 0mmol/L NaCl stress. (2) Additionally, there was slight difference in color of 5-day rice seedlings between NT and T3 (#1, #2, #3) which germinated under 125mmol/L NaCl stress. (3) Especially, there was a big difference in color of 5-day rice seedlings between NT and T3 (#1, #2, #3) which germinated under 150mmol/L and 175 mmol/L NaCl stress, in mesocotyl (S2). This result indicated that OsCu/Zn-SOD gene overexpression decreases oxidative stress damage and the T3 #1, #2, #3 lines had a certain tolerance to salt stress during germination stage, which were validated by the SOD scavenging activity of these lines.

(A) Phenotype. (B) Germination rate. (C) Plant fresh weight. (D) Plant height. (E) MDA content of NT and overexpression of OsCu/Zn-SOD Rice (T3-#1, #2, #3) after 9 days of germination and growth. Significant differences in parameters when a, b, c, d is p