Background

Tobacco (Nicotiana tabacum L.) is cultured worldwide as an industrial crop traditionally used for manufacturing cigarettes. Recently, tobacco seed oil had been demonstrated to be an appropriate feedstock for biodiesel production [1,2,3,4]. Tobacco is an oilseed plant with oil content ranging from 36 to 41% of seed dry weight [5, 6]. Fatty acid composition of tobacco seed oil shows a main presence of palmitic acid (8.83–12.3%), stearic acid (2.1–3.3%), oleic acid (9.97–11.69%), and linoleic acid (64.38–75.9%) [1, 7, 8]. Feedstock supply is one of the main limiting factors for biodiesel production. A high seed yield tobacco variety (Solaris) had been generated for seed oil production [9]. Life cycle analysis indicates that the production of Solaris tobacco biodiesel creates impacts that are similar to those that have been identified in biodiesel production from other crops [10]. In addition, the fuel properties of biodiesel, including cold-temperature flow characteristics, oxidative stability and NOx emissions, are other factors limiting the wide apply of biodiesel. Fuel properties of biodiesel are mostly dependent on the fatty acid composition of plant seed oil [11]. Thus, altering the fatty acid profile could improve fuel properties of biodiesel.

The high linoleic acid content makes biodiesel produced from tobacco seed oil more susceptible to oxidation, which would limit its use in traditional engine. The microsomal Δ12 oleate desaturase (1-acyl-2-oleoyl-sn-glycero-3-phosphocholine Δ12 desaturase or FAD2) desaturates oleic acid to linoleic acid in the ER. In the past few decades, FAD2 genes from a number of plant species had been cloned and characterized [12,13,14,15,16,17,18]. Previous study reported that suppression of the tobacco NtFAD2 gene by RNAi (RNA interference) could significantly increase the oleic acid content. Same strategy had been adopted to increase the oleic acid content in other oil seed crops, such as soybean [19], Brassica rapa [20], cotton [21], and peanut [22]. In addition, artificial microRNAs [23], TALENs (transcription activator-like effector nucleases) [24] and standard mutagenesis [25,26,27,28] methods were also used for FAD2 gene suppression.

Although RNAi and artificial microRNA are useful tools for gene functional characterization, the continuously inheritance requirement for the T-DNA construct limited the application of these technologies in plant genetic breeding [29]. Recently, CRISPR (clustered regularly interspaced short palindromic repeats)-Cas9 system has emerged as a robust and versatile tool for genome editing in a variety of organisms [30,31,32]. Critically different from RNAi and artificial microRNA technologies, which generate knock-down by repressing transcripts of the targeted genes, CRISPR-Cas9 system could produce defined gene knockout by altering the genomic DNA sequence [33, 34]. Most recently, CRISPR-Cas9 system had been successfully adopted to produce high oleic seed oil by knockout FAD2 genes in a variety of crop species, including Camelina sativa [35], peanut [36], Brassica napus [29], and soybean [37]. In this paper, we identified four FAD2 genes in tobacco genome. CRISPR-Cas9 vector was designed to specifically knockout the seed-type NtFAD2–2a and NtFAD2–2b genes. The fatty acid profile of the tobacco mutant seeds showed a high oleic acid and low linoleic acid phenotype. The high oleic acid mutant lines generated in this paper could be used as a valuable material for further seed lipid engineering.

Results

Four FAD2 genes were identified in tobacco genome

Using Arabidopsis FAD2 protein (NP_187819) as a query sequence, four FAD2 proteins were identified in tobacco genome. According to the sequence similarity, these four FAD2 protein coding genes were designated as NtFAD2–1a (XM_016657141), NtFAD2–1b (XM_016639420), NtFAD2–2a (NM_001326113), and NtFAD2–2b (XM_016659639). Previous studies demonstrated that FAD2 proteins contained six transmembrane domains and eight conserved histidine residues in three H boxes, which were essential for its endoplasmic reticulum (ER) localization and desaturase activity [12, 38]. Six transmembrane domains were predicted in all tobacco FAD2 proteins using TMpred software (https://embnet.vital-it.ch/software/TMPRED_form.html) [39]. In addition, protein sequence alignment showed that the putative transmembrane domains and H boxes of tobacco FAD2 proteins were identical to those regions reported in other FAD2 proteins (Fig. 1). FAD2 protein is an ER membrane-bound fatty acid desaturase, an ER retrieval motif is needed at the C-terminus for ER localization [40, 41]. Sequence analysis showed that tobacco FAD2 proteins contained the conserved ER localization signal (YKNKL) at the C-terminus (Fig. 1). In addition to the high levels of amino acid sequence similarity of tobacco FAD2 proteins, the coding regions also showed a relatively high level sequence identity (~ 85%) (Additional file 1: Figure. S1), which would make functional analysis through RNAi method a challenge.

Fig. 1
figure 1

Alignment of NtFAD2–1a, NtFAD2–1b, NtFAD2–2a, NtFAD2–2b, AtFAD2, and OsFAD2 protein sequences. Multiple sequence alignment was performed using DNAMAN 8.0. Black and gray shading indicate conserved and similar amino acids, respectively. Open boxes represent H boxes, while the transmembrane α-helices (TM) and endoplasmic reticulum (ER) localization signal are underlined

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Tobacco is a natural allotetraploid plant generated by the hybridization of N. sylvestris and N. tomentosiformis. In order to trace the origin of these four FAD2 genes, phylogenetic analysis was performed. Our result showed that NtFAD2–1a and NtFAD2–2a originated from N. tomentosiformis, while NtFAD2–1b and NtFAD2–2b originated from N. sylvestris (Additional file 1: Figure. S2).

NtFAD2–2a and NtFAD2–2b were seed-type FAD2 genes

To characterize the function of the tobacco FAD2 genes, real-time qRT-PCR was performed to investigate the expression profiles of NtFAD2 genes in various organs. Our results showed that NtFAD2–1a and NtFAD2–1b had a similar expression pattern, NtFAD2–2a and NtFAD2–2b had a similar expression profile, possibly due to the high levels of sequence identity of the promoter region (Additional file 1: Figure. S3). NtFAD2–1a and NtFAD2–1b genes were highly expressed in vegetative tissues and flowers, while the transcript abundance in developing seed was relatively low. NtFAD2–2a and NtFAD2–2b genes were detected in all organs, with the highest transcription level in developing seeds (Fig. 2). These results indicated that NtFAD2–2 genes might be mainly involved in the desaturation of seed storage lipids and NtFAD2–1 genes might play a more important role in vegetative organs and flowers cell membrane lipid desaturation.

Fig. 2
figure 2

Expression profile of tobacco FAD2 genes. R, root; L, leaf; S, stem; F, flower; S1, developing seed at 7 days after flowering (DAF); S2, developing seed at 15 DAF; S3, developing seed at 21 DAF. Data are mean ± SD of three biological replicates. NtGAPDH gene was amplified as an internal control

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Previous studies demonstrated that FAD2 genes could be classified into house-keeping type and seed-type based on phylogenetic analysis. The real time qRT-PCR results indicated that NtFAD2–2 genes belonged to the seed-type FAD2 genes. To further confirm this result, phylogenetic tree was constructed based on the protein sequence. Phylogenetic analysis showed that NtFAD2–1 genes were classified into house-keeping type. The NtFAD2–2 genes were classified into the same branch with the previously reported seed-type FAD2 genes from other oil crops, including sunflower, soybean, and cotton (Fig. 3). Taken together, these results demonstrated that tobacco NtFAD2–2 genes were seed-type FAD2 genes.

Fig. 3
figure 3

Phylogenetic analysis of FAD2 proteins from various plants. Phylogenetic tree was constructed using the MEGA5.0 software. The letters and numbers listed after FAD2 represent protein accession number. The letters preceding FAD2 indicate the initials of individual species, defined as follows: Ah, Arachis hypogaea; At, Arabidopsis thaliana; Bc, Brassica carinata; Gm, Glycine max; Gh, Gossypium hirsutum; Ha, Helianthus annuus; Oe, Olea europaea; Nt, Nicotiana tabacum

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NtFAD2–2 proteins showed Δ12 desaturase activity in yeast cells

Yeast (Saccharomyces cerevisiae) cells had been successfully used for functional characterization of FAD2 genes from a variety of plant species [16, 17, 42,43,44,45]. Due to the lack of FAD2-like genes, yeast cells cannot convert oleic acid into linoleic acid. To confirm the desaturation activity of the tobacco seed-type NtFAD2–2 proteins, the coding regions of NtFAD2–2a and NtFAD2–2b genes were cloned into the yeast expression vector pDR195 and expressed in yeast cells under the control of PMA1 promoter. Yeast cells transformed with the empty vector pDR195 contained only the typical yeast fatty acids, including C16:0, C16:1Δ9, C18:0, and C18:1Δ9 (Fig. 4a). Expression of both NtFAD2–2a and NtFAD2–2b genes resulted in two additional peaks in gas chromatograms, corresponding to C16:2Δ9, 12 and C18:2Δ9, 12 (Fig. 4b, Fig. 4c). In addition, the peak area of C16:1Δ9 and C18:1Δ9 in the NtFAD2–2 genes overexpressed yeast cells were noticeably smaller than the corresponding peak in the empty vector transformed cells, which might indicate the conversion of 16:1Δ9 and C18:1Δ9 into C16:2Δ9, 12 and C18:2Δ9, 12, respectively (Additional file 2: Table S1). Taken together, these results demonstrated that the seed-type NtFAD2–2a and NtFAD2–2b proteins had Δ12 desaturase activity in yeast cells.

Fig. 4
figure 4

GC-MS analysis of fatty acid methyl esters (FAMEs) from yeast cells expressing NtFAD2–2a and NtFAD2–2b. a, yeast cells transformed with pDR195 empty vector. b, yeast cells transformed with pDR195-NtFAD2–2a. c, yeast cells transformed with pDR195-NtFAD2–2b

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Generation of NtFAD2–2 knockout mutants using CRISPR-Cas9-mediated genome editing

To further investigate the role of NtFAD2–2 genes in tobacco seed fatty acid desaturation and to construct a high oleic acid tobacco seed oil material, we generated NtFAD2–2 knockout lines using CRISPR-Cas9-based genome editing method. Due to the high sequence identity of NtFAD2–2a and NtFAD2–2b genes, one gRNA targeting the coding sequence of both genes was designed using CRISPR-P 2.0 (Fig. 5a). The CRISPR/Cas9 construct was introduced into tobacco via the Agrobacterium-mediated transformation. Eighteen T0 transgenic lines were obtained by kanamycin selection and two independent homozygous mutated plants for both NtFAD2–2a and NtFAD2–2b genes (fad2–2#06 and fad2–2#14) were identified through Sanger sequencing. fad2–2#06 mutant had 1 bp deletion and fad2–2#14 had 5 bp deletion at 3 bp upstream of the protospacer adjacent motif (PAM) sequence (Fig. 5b, Fig. 5c), which all resulted in a premature stop codon. Using a PCR method, T-DNA construct free plants were selected from 20 T1 segregant plants generated from the self-pollination of each of the two mutant plants, respectively (Additional file 1: Figure. S4). Three T-DNA free homozygous mutant T1 plants from each mutant line were selected for phenotype analysis.

Fig. 5
figure 5

CRISPR-Cas9 mediated NtFAD2–2 genes mutation. a, Targeting site and gRNA sequence used for NtFAD2–2 genes editing. 19 bp gRNA sequence was underlined. The 3 base PAM sequence was in red. b, Sequences of wild type and representative mutation types induced at the targeting site of NtFAD2–2 were presented, respectively. c, DNA sequencing peaks of WT and representative mutation types at the targeting site of NtFAD2–2, respectively. The red arrows indicate the location of mutations

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Oleic acid content was increased in fad2–2 mutant seeds

Fatty acid profile of mature seeds derived from fad2–2 mutant plants were analyzed by GC-MS. Compared with the WT plants, seeds derived from both mutant lines showed the expected high oleic acid and low linoleic acid phenotype (Fig. 6). Oleic acid content was increased dramatically from ~ 12% in WT seeds to over 79% in both mutant lines (Fig. 7a). On the contrary, linoleic acid content was significantly reduced from 71.9% in WT plant seeds to 7.1–8.8% in both mutant lines (Fig. 7a). However, linoleic acid was still detected in both mutant lines, the remaining linoleic acid might be generated by the fatty acid desaturase activity provided by the low expression levels of NtFAD2–1 and plastidial FAD6 genes in developing seeds. Surprisingly, palmitic acid content was significantly reduced in the fad2–2 mutant seeds (Fig. 7a). The reduction of palmitic acid level was also observed in FAD2 suppressed peanut, soybean, and cotton [21, 37, 46], whereas the underlying mechanism of palmitic acid reduction was still unclear.

Fig. 6
figure 6

GC-MS analysis of fatty acid methyl esters (FAMEs) from WT and fad2–2 mutant tobacco seeds. a, Fatty acid profile of WT seeds. b, Fatty acid profile of fad2–2#06 mutant seeds. c, Fatty acid profile of fad2–2#14 mutant seeds

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Fig. 7
figure 7

Lipid analysis of WT and fad2–2 mutant seeds. a, fatty acid composition (mol %) of WT and fad2–2 mutant seeds. Data are mean ± SD (n = 3). Asterisks indicate significant difference compared to the corresponding controls determined by one-way ANOVA with Dunnett’s test (*P < 0.05; **P < 0.01). b, Lipid content per seed. Data are mean ± SD (n = 3)

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Previous study showed that the high-oleic acid phenotype of RNAi mediated FAD2-silenced tobacco was abated by lower temperature, and the author suggested that the instability of the high-oleic acid phenotype must be partially due to activities of plastidial desaturases [47]. Thus, we examined the fatty acid composition of low temperature treated WT and fad2–2 mutant seeds, our results showed that the WT seeds showed an increased level of linoleic acid content under low temperature, however, the high-oleic phenotype of fad2–2 mutant seeds was not affected by low temperature (Table 1).

Table 1 Fatty acid composition (mol%) of tobacco seeds from wild type and fad2–2 mutant plants
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Lipid content was not affected in fad2–2 mutant seeds

Seed lipid is stored mainly in the form of triacylglycerol (TAG) in oilseed. Due to the inefficient utilization of the engineered fatty acid profile, previous studies showed that total TAG production was usually reduced in multiple genetically modified plant seeds [48,49,50]. Thus we examined the total lipid content of fad2–2 mutant seeds. Unexpectedly, the lipid content was not affected in both fad2–2 mutant lines (Fig. 7b), which indicated that the increased oleic acid could be efficiently incorporated into TAG.

Seed size and seed weight of oil plants were generally positively correlated with seed lipid content [51,52,53]. We further examined the seed size and weight of WT and fad2–2 mutant lines. Our results showed that seed size and seed weight were not affected by NtFAD2–2 genes mutation (Additional file 1: Figure S5). These results were consistent with the seed lipid content.

Fatty acid profile of leaf was not changed in fad2–2 mutants

The house-keeping NtFAD2–1a and NtFAD2–1b genes sequence were highly similar with the seed-type NtFAD2–2a and NtFAD2–2b genes (Additional file 1: Figure. S1). Probably due to the unspecific property, RNAi mediated FAD2 genes silencing in tobacco led to increased oleic acid content in leaf fatty acid profile [54], which might affect the stress tolerance of genetically modified plants. In this present paper, we identified NtFAD2–2a and NtFAD2–2b as seed-type FAD2 genes and created fad2–2 mutant through high specific CRISPR-Cas9 system. We suggested that mutation of the seed-type NtFAD2–2 genes will not affect the fatty acid desaturation in tobacco leaves, because of the function redundancy of NtFAD2–1 genes in vegetative tissues. In order to confirm this possibility, we examined the leaf fatty acid profile of WT and fad2–2 mutant lines. The GC-MS results showed that fatty acid composition of leaves from fad2–2 mutant lines were comparable with that of WT plant (Table 2). Our results indicated that editing the seed-type FAD2 genes by CRISPR-Cas9 system was a feasible way to engineer the tobacco seed oil without affecting the vegetative tissues.

Table 2 fatty acid composition of tobacco leaf from wild type and fad2–2 mutant plants
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Discussion

Tobacco seed-type FAD2 genes could be used as the target for seed fatty acid profile engineering

Due to the high oil content, tobacco seed was proposed to be a promising feedstock for biodiesel production [2, 4, 9]. However, the high linoleic acid content of tobacco seed oil is problematic from the perspective of oxidative stability, which is important for industrial applications [1, 3]. Low linoleic acid and high oleic acid content are preferred in nearly all oil seed crops breeding, and high oleic acid cultivars have been generated by selecting for or engineering reduced FAD2 activity [55]. In this paper, four FAD2 genes were firstly identified from tobacco genome (Fig. 1). Both gene expression analysis and phylogenetic analysis showed that NtFAD2–2a and NtFAD2–2b were seed-type FAD2 genes (Fig. 2, Fig. 3). Knockout of NtFAD2–2 genes by CRISPR-Cas9 system led to a high oleic acid and low linoleic acid phenotype in tobacco seed oil (Fig. 6, Fig. 7a). In addition, the leaf fatty acid compositions of NtFAD2–2 genes edited plant were not affected (Table 2). Our results indicated that seed-type NtFAD2–2 genes were ideal targets for high oleic acid tobacco seed oil breeding.

CRISPR-Cas9 system was a useful tool for tobacco breeding

The influence of temperature on the polyunsaturated fatty acid content of storage lipids, which was observed in a number of oilseed crops [56, 57], is considered to be undesirable, since it leads to variation in product quality [58]. Temperature was proposed to affect fatty acid desaturation by regulating the expression of FAD2 gene [59,60,61,62] or influencing the rate of FAD2 protein turnover [63,64,65,66]. Previous study showed that the high-oleic acid phenotype of FAD2-silenced tobacco was abated at lower temperature [47]. Our results demonstrated that knockout of the tobacco seed-type NtFAD2–2 genes using the CRISPR-Cas9 system could get a stable and high oleic acid tobacco seed oil (Table 2).

FAD2 catalyzed fatty acid desaturation is a key step in biosynthesis of polyunsaturated fatty acids, including linolenic acid, which is important in maintaining cellular function. Previous studies have demonstrated that FAD2 genes play crucial roles in response to various abiotic stresses, such as chilling temperature [60, 67,68,69] and salt [70]. Most recently, FAD2 genes were demonstrated to be responsible for biotic stress in tomato [55]. The house-keeping NtFAD2–1 genes sequence were highly similar with the seed-type NtFAD2–2 genes. Probably due to the low specificity of RNAi-mediated gene silencing method, the fatty acid composition of transgenic tobacco leaf was also altered, which might affect the stress tolerance of transgenic lines [47, 54]. CRISPR-Cas9 system mediated gene knockout is more specific, our results showed that fatty acid profile of leaves from mutant lines were not affected (Table 2). Thus, the high oleic acid tobacco mutant lines generated by CRISPR-Cas9 system had no side effects and could be used as basal material for further lipid engineering.

Tobacco fad2–2 mutant lines could be further engineered to accumulate unusual fatty acid

FAD2 protein adds a double bond at the Δ12 position of oleic acid. Plants accumulating unusual fatty acids possess divergent forms of the Δ12-desaturase (FAD2) that are able to catalyze alternative modifications at the Δ12 position of oleic acid, such as the formation of a carbon-carbon triple bond or a conjugated double bond arrangement, or the insertion of an epoxy bridge or hydroxyl group. Due to the unique physical and chemical properties, unusual fatty acids could be used as additives or raw materials for numerous industrial products, such as lubricants, plastics, and inks [71]. However, unusual fatty acids are mainly produced in plants which has not been domesticated as crops, such as castor bean and tung tree. In order to meet the increasingly need, recent research efforts have been focused on engineering desirable unusual fatty acids using biotechnology in existing oilseeds [71,72,73]. sn-2- 18:1-PC is used as substrate for both FAD2 and divergent forms of FAD2 proteins. In order to maximum the production of unusual fatty acids, the endogenous FAD2 activity has to be abolished. In this paper, high-oleic acid tobacco seed oil mutants was generated by CRISPR-Cas9 system, and these mutant lines could be used for unusual fatty aicds engineering.

Conclusion

In summary, four FAD2 genes were identified in tobacco genome for the first time, and NtFAD2–2a and NtFAD2–2b genes were confirmed to be seed-type FAD2 genes. Compared with the RNAi technology, two stable and high-oleic acid tobacco seed oil lines were generated using CRISPR-Cas9-mediated gene knockout method. In addition, the leaf fatty acid profile of the mutants created by CRISPR-Cas9 system was not affected. The mutants generated in this present study could be used for advanced engineering to produce unusual fatty acid.

Methods

Plant materials and growth condition

Wild type (WT) tobacco (Nicotiana tabacum L. cv. K326) was provided by the Yunnan Academy of Tobacco Agriculture Science (http://ynycnky.yn-tobacco.com/). Dr. Changjun Huang from Key Laboratory of Tobacco Biotechnological Breeding in Yunnan Academy of Tobacco Agriculture Science undertook the formal identification of the samples and provided details of specimen deposited. WT tobacco was used for genetic transformation. WT and transgenic or mutant tobacco plants were grown in the greenhouse at 25 °C with 16 h light and 8 h dark. For low temperature treatment, developing seeds at 20 days after pollination were collected and cultivated on 1/2 MS medium supplemented with 2% sucrose at 18 °C for 24 h in the dark. The control treatment temperature was 25 °C.

Isolation and sequence analysis of FAD2 genes in tobacco

To identify the putative FAD2 genes in tobacco, Arabidopsis FAD2 protein (accession number: NP_187819) was used as a query sequence to blast against the tobacco genome database (https://solgenomics.net/organism/Nicotiana_tabacum/genome) under the default parameters. Homologous protein sequences with an identity score higher than 70% were chosen for further analysis. The target sequences were further confirmed through BLAST program at National Center for Biotechnology Information (NCBI). Sequence alignment was performed with DNAMAN software. Phylogenetic tree was constructed with the neighbor-joining algorithm using the MEGA5.0 [74]. Bootstrap analysis with 1000 replicates was performed to test the significance of nodes.

RNA isolation and quantitative RT-PCR (qRT-PCR)

Plant tissues were sampled and ground immediately in liquid N2, total RNA was extracted using the Plant Total RNA Isolation Kit (Foregene, China) and reverse-transcribed into cDNA with PrimeScript™ RT reagent Kit (Takara, Dalian). qRT-PCR program was performed using SYBR Premix Ex Taq™ II (Tli RNaseH Plus) (Takara, Dalian) on a CFX96 real-time PCR system (Bio-Rad, USA). The qRT-PCR cycling began with one cycle at 95 °C for 2 min, followed by 40 cycles at 95 °C for 30 s, 55 °C for 30 s, 72 °C for 30 s. The house-keeping gene, NtGAPDH (XM_016643257), was used as the internal control. Three biological and three technical replicates were performed. All primer used for qRT-PCR were listed in Additional file 2: Table S2.

Expression of NtFAD2–2 genes in S. cerevisiae

The coding regions of NtFAD2–2a and NtFAD2–2b genes were amplified and inserted into pDR195 vector. The reconstructed vectors were named as pDR195:NtFAD2–2a and pDR195:NtFAD2–2b, respectively. The BY4741 strain of Saccharomyces cerevisiae was transformed with these vectors using the lithium acetate method and selected on minimal agar plates lacking uracil [75]. Isolated colonies were inoculated in 10 ml complete minimal drop out-Uracil medium containing 2% glucose. When the culture reached at stationary phase, yeast cells were harvested by centrifugation at 1500 g for 5 min at 4 °C, and washed once with distilled water. Primers used for vectors construction were listed in Additional file 2: Table S2.

Vector construction

For CRISPR-Cas9 vector construction, guide RNA (gRNA) targeting the coding region of NtFAD2–2 genes was designed using a CRISPR-P 2.0 (http://crispr.hzau.edu.cn/CRISPR2/) [76]. gRNA was inserted into the pKSE401 vector using Golden-gate assembly method as described previously [77]. The reconstructed vector (named as pKSE401-NtFAD2–2) was confirmed using the Sanger sequencing and introduced into Agrobacterium tumefaciens strain GV3101. Primers used for vectors construction were listed in Additional file 2: Table S2.

Tobacco genetic transformation and selection

Transgenic tobacco was generated by the Agrobacterium-mediated transformation as previously reported [78]. T0 generation lines were selected on media with 50 mg/L kanamycin. Mutation selection was performed as previous reported with some modification [79]. Briefly, genomic DNA was extracted from the leaves of the kanamycin-resistant T0 transgenic plants using the Plant DNA Isolation Kit (Foregene, China). To select mutant transgenic plants, PCR amplification was performed using a primer pair flanking the gRNA target site of NtFAD2–2 loci (the forward primer annealing at 39 bp downstream of the start codon, and the reverse primer annealing at 441 bp downstream of the start codon), and the generated PCR products were directly sequenced using the Sanger method. Mutant plants were selected by comparing the amplicon sequences and the WT template. Twenty T1 segregant plants generated from the self-pollination of T0 mutated plants were screened for the presence/absence of the T-DNA using PCR assay directed to the Cas9 gene sequence. Three T-DNA free homozygous mutant T1 plants were selected for phenotype analysis. The PCR primers used in these steps are listed in Additional file 2: Table S2.

Lipid analysis

To analyze lipids from yeast cells, tobacco leaves, and tobacco seeds, fatty acid methyl esters (FAMEs) were prepared as previously described [80], and then quantitatively analyzed by gas chromatography mass spectrometry (GC-MS) (GC-2010, DAOJING). The GC conditions were as follows: split injection (1: 20), injector temperature 220 °C, oven temperature program 150 °C for 1 min, then increasing by 10 °C min− 1 to 200 °C, holding at 200 °C for 1 min, then increasing by 5 °C min− 1 to 210 °C, held for 1 min.

Seed weight and size measurement

Mature seeds were harvested from WT and mutant tobacco plants grown under the same conditions. Fifty seeds per group were weighed carefully on analytical balance, per seed weight was calculated by dividing the seed number. Values were given as mean ± SD. Mature seeds were photographed with a stereoscopic microscope (Leica, Germany) and Image J software was used to measure the seed size. Values were given as mean ± SD.