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Effects of 1-methylcyclopropene on skin greasiness and quality of ‘Yuluxiang’ pear during storage at 20°C
Wanting Yu, Xinnan Zhang, Weiwei Yan, Xiaonan Sun, Yang Wang, Xiaohui Jia
2024, 23 (7): 2476-2490.   DOI: 10.1016/j.jia.2024.03.017
Abstract83)      PDF in ScienceDirect      

During storage at 20°C, specific pear cultivars may exhibit a greasy texture and decline in quality due to fruit senescence. Among these varieties, ‘Yuluxiang’ is particularly susceptible to peel greasiness, resulting in significant economic losses. Therefore, there is an urgent need for a preservative that can effectively inhibit the development of greasiness. Previous studies have demonstrated the efficacy of 1-methylcyclopropene (1- MCP) in extending the storage period of fruits. We hypothesize that it may also influence the occurrence of postharvest peel greasiness in the ‘Yuluxiang’ pears. In this study, we treated ‘Yuluxiang’ pears with 1-MCP. We stored them at 20°C while analyzing the composition and morphology of the surface waxes, recording enzyme activities related to wax synthesis, and measuring indicators associated with fruit storage quality and physiological characteristics. The results demonstrate that prolonged storage at 20°C leads to a rapid increase in skin greasiness, consistent with the observed elevations in L*, greasiness score, and the content of total wax and greasy wax components. Moreover, there were indications that cuticular waxes underwent melting, resulting in the formation of an amorphous structure. In comparison to controls, the application of 1-MCP significantly inhibited increments in L* values as well as grease scores while also reducing accumulation rates for oily waxes throughout most stages over its shelf period, additionally delaying transitions from flaky-wax structures towards their amorphous counterparts. During the initial 7 d of storage, several enzymes involved in the biosynthesis and metabolism of greasy wax components, including lipoxygenase (LOX), phospholipase D (PLD), and β-ketoacyl-CoA synthase (KCS), exhibited an increase followed by a subsequent decline. The activity of LOX during early shelf life (0–7 d) and the KCS activity during middle to late shelf life (14–21 d) were significantly suppressed by 1-MCP. Additionally, 1-MCP effectively maintained firmness, total soluble solid (TSS) and titratable acid (TA) contents, peroxidase (POD), and phenylalanine ammonia-lyase (PAL) activities while inhibiting vitamin C degradation and weight loss. Furthermore, it restrained polyphenol oxidase (PPO) activity, ethylene production, and respiration rate increase. These findings demonstrate that 1-MCP not only delays the onset of peel greasiness but also preserves the overall storage quality of ‘Yuluxiang’ pear at a temperature of 20°C. This study presents a novel approach for developing new preservatives to inhibit pear fruit peel greasiness and provides a theoretical foundation for further research on pear fruit preservation.

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Upregulation of the glycine-rich protein-encoding gene GhGRPL enhances plant tolerance to abiotic and biotic stressors by promoting secondary cell wall development
Wanting Yu, Yonglu Dai, Junmin Chen, Aimin Liang, Yiping Wu, Qingwei Suo, Zhong Chen, Xingying Yan, Chuannan Wang, Hanyan Lai, Fanlong Wang, Jingyi Zhang, Qinzhao Liu, Yi Wang, Yaohua Li, Lingfang Ran, Jie Xiang, Zhiwu Pei, Yuehua Xiao, Jianyan Zeng
2024, 23 (10): 3311-3327.   DOI: 10.1016/j.jia.2024.05.025
Abstract93)      PDF in ScienceDirect      
Abiotic and biotic stressors adversely affect plant survival, biomass generation, and crop yields.  As the global availability of arable land declines and the impacts of global warming intensify, such stressors may have increasingly pronounced effects on agricultural productivity.  Currently, researchers face the overarching challenge of comprehensively enhancing plant resilience to abiotic and biotic stressors.  The secondary cell wall plays a crucial role in bolstering the stress resistance of plants.  To increase plant resistance to stress through genetic manipulation of the secondary cell wall, we cloned a cell wall protein designated glycine-rich protein-like (GhGRPL) from cotton fibers, and found that it is specifically expressed during the period of secondary cell wall biosynthesis.  Notably, this protein differs from its Arabidopsis homolog, AtGRP, since its glycine-rich domain is deficient in glycine residues.  GhGRPL is involved in secondary cell wall deposition.  Upregulation of GhGRPL enhances lignin accumulation and, consequently, the thickness of the secondary cell walls, thereby increasing the plant’s resistance to abiotic stressors, such as drought and salinity, and biotic threats, including Verticillium dahliae infection.  Conversely, interference with GhGRPL expression in cotton reduces lignin accumulation and compromises that resistance.  Taken together, our findings elucidate the role of GhGRPL in regulating secondary cell wall development through its influence on lignin deposition, which, in turn, reinforces cell wall robustness and impermeability.  These findings highlight the promising near-future prospect of adopting GhGRPL as a viable, effective approach for enhancing plant resilience to abiotic and biotic stress factors.


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Specific expression of a fusion gene Lc-GhPAP1D results in colored cotton fibers with increased flavonoid and lignin synthesis, but impaired elongation and secondary cell wall deposition
Lingfang Ran, Yaohua Li, Long Chen, Tong Mo, Nian Liu, Shijia Xu, Yucheng Su, Chuannan Wang, Aimin Liang, Jianyan Zeng, Wanting Yu, Jie Kong, Yuehua Xiao
DOI: 10.1016/j.jia.2025.02.044 Online: 21 February 2025
Abstract5)      PDF in ScienceDirect      

Naturally colored cotton (NCC) represents a kind of eco-friendly and sustainable textile material. Limited colors and inferior yield and quality are the major obstacles to the wide application of NCCs.  The present work aimed to generate new colored cotton by synthesizing and accumulating anthocyanins in fibers.  Two anthocyanin regulatory genes Lc and GhPAP1D were fused and specifically expressed in fibers of the secondary cell wall (SCW) stage.  The transgenic fibers exhibited pronounced purplish-red color at 20 to 30 DPA (days post anthesis), and reddish-brown color at maturation.  Meanwhile, expressing Lc and GhPAP1D led to reduced elongation rate and impaired SCW deposition in fibers, finally decreased fiber strength and length, and low lint percentage at maturation.  Metabolomic and transcriptomic analyses indicated that the whole flavonoid pathway was significantly up-regulated, and multiple flavonoids, including anthocyanins, proanthocyanidins and flavonols, were accumulated in developing and mature fibers.  It was also found that lignin biosynthesis and accumulation were significantly increased in fibers of the SCW synthesis stage.  Our results provided a feasible strategy to promote anthocyanin synthesis and accumulation in cotton fibers, and also its side effects on fiber coloration and development, which laid the foundation for future NCC color innovation.

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Phase-specific enhancement of carotenoids and abscisic acid promotes secondary cell wall synthesis by activating key transcription factors and ethylene biosynthesis in cotton fiber
Chuannan Wang, Baitao Liu, Jianyan Zeng, Yaohua Li, Wanting Yu, Qingwei Suo, Lingfang Ran, Long Chen, Yi Wang, Aimin Liang, Jie Kong, Yuehua Xiao
DOI: 10.1016/j.jia.2025.04.006 Online: 07 April 2025
Abstract11)      PDF in ScienceDirect      
 Cotton (Gossypium) is an important economic crop providing most of the natural fiber for the global textile industry.  The secondary cell wall (SCW) comprises the major dry weight of cotton fiber, and is a key determinant of cotton yield and quality.  In this study, a fiber-specific promoter, proFbl2A, was employed to control the expression of a fusion gene of phytoene synthase and 1-deoxy-D-xylulose-5-phosphate synthase (GhPSY2D and GhDXS6D, respectively) in cotton fibers of the SCW synthesis stage, resulting in higher carotenoid and abscisic acid (ABA) levels in the transgenic cotton fibers.  The SCW synthesis initiated earlier in the ABA-up-regulated cotton fibers than the wild-type control, along with the expression of SCW stage-specific genes and key SCW regulators.  Consistently, several positive bZIP transcription factors of ABA signaling (GhbZIP27b, GhbZIP37b, and GhbZIP66b), were found to bind to and activate the promoters of key SCW regulators (GhTCP4A, GhFSN1, and GhMYB7D).  Furthermore, these bZIPs could also interact with and promote the expression of two ethylene synthase genes (GhACS10 and GhACO3).  Our data demonstrated that enhancement of carotenoid and ABA could advance SCW initiation by activating key transcription factors, and promote SCW thickening via ethylene biosynthesis in cotton fibers. 
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