Abstract
Carbon monoxide (CO) represents one of key gasotransmitter molecules involved in transduction of various signals necessary for regulation of many functions of living organisms. The review considers peculiarities of CO synthesis in plants and briefly characterizes heme oxygenase as a chief enzyme catalyzing the formation of carbon monoxide. Participation of CO in the processes of growth and development, in particular, seed germination, root formation, and senescence is discussed. Special attention is paid to the role of carbon monoxide in the formation of adaptive reactions to stressors of various nature. Mediation of CO-dependent biological effects by calcium ions, ROS, and nitric oxide is considered. In addition, the involvement of carbon monoxide in the action of other signal molecules, including phytohormones, is analyzed. The properties of the CO donors are briefly surveyed, and their possible value for biological experiments is assessed.
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REFERENCES
Wang, R., Overview of gasotransmitters and the related signaling network, in Gasotransmitters, Wang, R., Ed., Cambridge: R. Soc. Chem., 2018, ch. 1, p. 1. https://doi.org/10.1039/9781788013000-00001
Yao, Y., Yang, Y., Li, C., Huang, D., Zhang, J., Wang, C., Li, W., Wang, N., Deng, Y., and Liao, W., Research progress on the functions of gasotransmitters in plant responses to abiotic stresses, Plants, 2019, vol. 8, p. 605. https://doi.org/10.3390/plants8120605
Karle, S.B., Guru, A., Dwivedi, P., and Kumar, K., Insights into the role of gasotransmitters mediating salt stress responses in plants, J. Plant Growth Regul., 2021, vol. 40, p. 2259. https://doi.org/10.1007/s00344-020-10293-z
Takagi, T., Uchiyama, K., and Naito, Y., The therapeutic potential of carbon monoxide for inflammatory bowel disease, Digestion, 2015, vol. 91, p. 13. https://doi.org/10.1159/000368765
Motterlini, R. and Foresti, R., Biological signaling by carbon monoxide and carbon monoxide-releasing molecules, Am. J. Physiol. Cell Physiol., 2017, vol. 312, p. 302. https://doi.org/10.1152/ajpcell.00360.2016
Wilks, S.S., Carbon monoxide in green plants, Science, 1959, vol. 129, p. 964. https://doi.org/10.1126/science.129.3354.964
Pandey, A.K. and Gautam, A., Stress responsive gene regulation in relation to hydrogen sulfide in plants under abiotic stress, Physiol. Plant., 2020, vol. 168, p. 511. https://doi.org/10.1111/ppl.13064
Mishra, V., Singh, P., Tripathi, D.K., Corpas, F.J., and Singh, V.P., Nitric oxide and hydrogen sulfide: an indispensable combination for plant functioning, Trends Plant Sci., 2021, vol. 26, p. 1270. https://doi.org/10.1016/j.tplants.2021.07.016
Feelisch, M. and Olson, K.R., Embracing sulfide and CO to understand nitric oxide biology, Nitric Oxide, 2013, vol. 35, p. 2. https://doi.org/10.1016/j.niox.2013.06.004
Santa-Cruz, D.M., Pacienza, N.A., Polizio, A.H., Balestrasse, K.B., Tomaro, M.L., and Yannarelli, G.G., Nitric oxide synthase-like dependent NO production enhances heme oxygenase up-regulation in ultraviolet-B-irradiated soybean plants, Phytochemistry, 2010, vol. 71, p. 1700. https://doi.org/10.1016/j.phytochem.2010.07.009
Lin, Y.T., Zhang, W., Qi, F., Cui, W.T., Xie, Y.J., and Shen, W.B., Hydrogen-rich water regulates cucumber adventitious root development in a heme oxygenase-1/carbon monoxide-dependent manner, J. Plant Physiol., 2014, vol. 171, p. 1. https://doi.org/10.1016/j.jplph.2013.08.009
Dekker, J. and Hargrove, M., Weedy adaptation in Setaria spp, vol. effects of gaseous environment on giant foxtail (Setaria faberii) (Poaceae) seed germination, Am. J. Bot., 2002, vol. 89, p. 410. https://doi.org/10.3732/ajb.89.3.410
Cao, Z., Xuan, W., Liu, Z., Li, X., Zhao, N., Xu, P., Wang, Z., Guan, R., and Shen, W., Carbon monoxide promotes lateral root formation in rapeseed, J. Integr. Plant Biol., 2007, vol. 49, p. 1070. https://doi.org/10.1111/j.1672-9072.2007.00482.x
Chen, Y.H., Chao, Y.Y., Hsu, Y.Y., Hong, C.Y., and Kao, C.H., Heme oxygenase is involved in nitric oxide- and auxin-induced lateral root formation in rice, Plant Cell Rep., 2012, vol. 31, p. 1085. https://doi.org/10.1007/s00299-012-1228-x
Cui, W.T., Qi, F., Zhang, Y.H., Cao, H., Zhang, J., Wang, R., and Shen, W., Methane-rich water induces cucumber adventitious rooting through heme oxygenase1/carbon monoxide and Ca2+ pathways, Plant Cell Rep., 2015, vol. 34, p. 435. https://doi.org/10.1007/s00299-014-1723-3
Huang, J., Han, B., Xu, S., Zhou, M., and Shen, W., Heme oxygenase-1 is involved in the cytokinin-induced alleviation of senescence in detached wheat leaves during dark incubation, J. Plant Physiol., 2011, vol. 168, p. 768. https://doi.org/10.1016/j.jplph.2010.10.010
Zhang, S., Li, Q., and Mao, Y., Effect of carbon monoxide on active oxygen metabolism of postharvest Jujube, J. Food Technol. Res., 2014, vol. 1, p. 146. https://doi.org/10.18488/journal.58/2014.1.2/58.2.146.155
Gahir, S., Bharath, P., and Raghavendra, A.S., The role of gasotransmitters in movement of stomata: mechanisms of action and importance for plant immunity, Biol. Plant, 2020, vol. 64, p. 623. https://doi.org/10.32615/bp.2020.071
He, H. and He, L.F., Regulation of gaseous signaling molecules on proline metabolism in plants, Plant Cell Rep., 2018, vol. 37, p. 387. https://doi.org/10.1007/s00299-017-2239-4
Shekhawat, G.S. and Verma, K., Haem oxygenase (HO): an overlooked enzyme of plant metabolism and defence, J. Exp. Bot., 2010, vol. 61, p. 2255. https://doi.org/10.1093/jxb/erq074
Bilban, M., Haschemi, A., Wegiel, B., Chin, B.Y., Wagner, O., and Otterbein, L.E., Heme oxygenase and carbon monoxide initiate homeostatic signaling, J. Mol. Med., 2008, vol. 86, p. 267. https://doi.org/10.1007/s00109-007-0276-0
Verma, K. and Alam, A., Heme oxygenase 1 (HO1): an enzyme of plant system and its role against various abiotic stresses, in Sustainable Agriculture in the Era of Climate Change, Roychowdhury, R., Choudhury, S., Hasanuzzaman, M., and Srivastava, S., Eds., Cham: Springer-Verlag, 2020, p. 355. https://doi.org/10.1007/978-3-030-45669-6_16
Wang, M. and Liao, W., Carbon monoxide as a signaling molecule in plants, Front. Plant Sci., 2016, vol. 7, p. 572. https://doi.org/10.3389/fpls.2016.00572
Terry, M.J., Linley, P.J., and Kohchi, T., Making light of it: the role of plant heme oxygenases in phytochrome chromophore synthesis, Biochem. Soc. Transact., 2002, vol. 30, p. 604.
Emborg, T.J., Walker, J.M., Noh, B., and Vierstra, R.D., Multiple heme oxygenase family members contribute to the biosynthesis of the phytochrome chromophore in Arabidopsis, Plant Physiol., 2006, vol. 140, p. 856. https://doi.org/10.1104/pp.105.074211
Balestrasse, K.B., Yannarelli, G.G., Noriega, G.O., Batlle, A., and Tomaro, M.L., Heme oxygenase and catalase gene expression in nodules and roots of soybean plants subjected to cadmium stress, Biometals, 2008, vol. 21, p. 433. https://doi.org/10.1007/s10534-008-9132-0
Davis, S., Bhoo, S.H., Durski, A.M., Walker, J.M., and Viersta, R.D., The heme oxygenase family required for phytochrome chromophore biosynthesis is necessary for proper photomorphogenesis in higher plants, Plant Physiol., 2001, vol. 126, p. 656. https://doi.org/10.1104/pp.126.2.65
Matsumoto, F., Obayashi, T., Sasaki-Sekimoto, Y., Ohta, H., Takamiya, K.-I., and Masuda, T., Gene expression profiling of the tetrapyrrole metabolic pathway in Arabidopsis with a mini-array system, Plant Physiol., 2004, vol. 135, p. 2379. https://doi.org/10.1104/pp.104.042408
Otterbein, L.E., Soares, M.P., Yamashita, K., and Bach, F.H., Heme oxygenase-1: unleashing the protective properties of heme, Trends Immunol., 2003, vol. 24, p. 449. https://doi.org/10.1016/s1471-4906(03)00181-9
Liu, Y., Xu, S., Ling, T., Xu, L., and Shen, W., Heme oxygenase/carbon monoxide system participates in regulating wheat seed germination under osmotic stress involving the nitric oxide pathway, J. Plant Physiol., 2010, vol. 167, p. 1371. https://doi.org/10.1016/j.jplph.2010.05.021
Xie, Y., Ling, T., Han, Y., Liu, K., Zheng, Q., Huang, L., Yuan, X., He, Z., Hu, B., Fang, L., Shen, Z., Yang, Q., and Shen, W., Carbon monoxide enhances salt tolerance by nitric oxide-mediated maintenance of ion homeostasis and up-regulation of antioxidant defence in wheat seedling roots, Plant Cell Environ., 2008, vol. 31, p. 1864. https://doi.org/10.1111/j.1365-3040.2008.01888.x
Han, Y., Zhang, J., Chen, X., Gao, Z., Xuan, W., Xu, S., Ding, X., and Shen, W., Carbon monoxide alleviates cadmium-induced oxidative damage by modulating glutathione metabolism in the roots of Medicago sativa, New Phytol., 2008, vol. 177, p. 155. https://doi.org/10.1111/j.1469-8137.2007.02251.x
Yannarelli, G.G., Noriega, G.O., Batlle, A., and Tomaro, M.L., Heme oxygenase up regulation in ultraviolet-B irradiated soybean plants involves reactive oxygen species, Planta, 2006, vol. 224, p. 1154. https://doi.org/10.1007/s00425-006-0297-x
Muramoto, T., Kohchi, T., Yokota, A., Hwang, I., and Goodman, H.M., The Arabidopsis photomorphogenic mutant hy1 is deficient in phytochrome chromophore biosynthesis as a result of a mutation in a plastid heme oxygenase, Plant Cell, 1999, vol. 11, p. 335. https://doi.org/10.1105/tpc.11.3.335
Dixit, S., Verma, K., and Shekhawat, G.S., In vitro evaluation of mitochondrial-chloroplast subcellular localization of heme oxygenase1 (HO1) in Glycine max, Protoplasma, 2014, vol. 251, p. 671. https://doi.org/10.1007/s00709-013-0569-9
Zilli, C.G., Santa-Cruz, D.M., and Balestrasse, K.B., Heme oxygenase-independent endogenous production of carbon monoxide by soybean plants subjected to salt stress, Environ. Exp. Bot., 2014, vol. 102, p. 11. https://doi.org/10.1016/j.envexpbot.2014.01.012
Jin, Q., Cui, W., Xie, Y., and Shen, W., Carbon monoxide: a ubiquitous gaseous signaling molecule in plants, in Gasotransmitters in Plants Signaling and Communication in Plants, Lamattina, L. and Garcia-Mata, C., Eds., Cham: Springer-Verlag, 2016, p. 3. https://doi.org/10.1007/978-3-319-40713-5_1
Liu, K., Xu, S., Xuan, W., Ling, T., Cao, Z., Huang, B., Sun, Y., Fang, L., Liu, Z., Zhao, N., and Shen, W., Carbon monoxide counteracts the inhibition of seed germination and alleviates oxidative damage caused by salt stress in Oryza sativa, Plant Sci., 2007, vol. 172, p. 544. https://doi.org/10.1016/j.plantsci.2006.11.007
Guo, K., Xia, K., and Yang, Z.M., Regulation of tomato lateral root development by carbon monoxide and involvement in auxin and nitric oxide, J. Exp. Bot., 2008, vol. 59, p. 3443. https://doi.org/10.1093/jxb/ern194
Guo, K., Kong, W.W., and Yang, Z.M., Carbon monoxide promotes root hair development in tomato, Plant Cell Environ., 2009, vol. 32, p. 1033. https://doi.org/10.1111/j.1365-3040.2009.01986.x
Amooaghaie, R., Tabatabaei, F., and Ahadi, A., Alterations in HO-1 expression, heme oxygenase activity and endogenous NO homeostasis modulate antioxidant responses of Brassica nigra against nano silver toxicity, J. Plant Physiol., 2018, vol. 228, p. 75. https://doi.org/10.1016/j.jplph.2018.01.012
He, D., Deng, G., Ying, S., Yang, W., Wei, J., and Li, P., Carbon monoxide signal breaks primary seed dormancy by transcriptional silence of DOG1 in Arabidopsis thaliana, Phyton, 2020, vol. 89, p. 633. https://doi.org/10.32604/phyton.2020.010498
Jia, Y., Li, R., Yang, W., Chen, Z., and Hu, X., Carbon monoxide signal regulates light-initiated seed germination by suppressing SOM expression, Plant Sci., 2018, vol. 272, p. 88. https://doi.org/10.1016/j.plantsci.2018.04.009
Xuan, W., Huang, L., Li, M., Huang, B., Xu, S., Liu, H., Gao, Y., and Shen, W., Induction of growth elongation in wheat root segments by heme molecules: a regulatory role of carbon monoxide in plants? Plant Growth Regul., 2007, vol. 52, p. 41. https://doi.org/10.1007/s10725-007-9175-1
Xuan, W., Xu, S., Yuan, X., and Shen, W., Carbon monoxide. A novel and pivotal signal molecule in plants? Plant Signaling Behav., 2008, vol. 3, p. 381. https://doi.org/10.4161/psb.3.6.5374
Xuan, W., Zhu, F.-Y., Xu, S., Huang, B.-K., Ling, T.-F., Qi, J.-Y., Ye, M.-B., and Shen, W.-B., The heme oxygenase/carbon monoxide system is involved in the auxin-induced cucumber adventitious rooting process, Plant Physiol., 2008, vol. 148, p. 881. https://doi.org/10.1104/pp.108.125567
Hsu, Y.Y., Chao, Y.-Y., and Kao, C.H., Methyl jasmonate-induced lateral root formation in rice: the role of heme oxygenase and calcium, J. Plant Physiol., 2013, vol. 170, p. 63. https://doi.org/10.1016/j.jplph.2012.08.015
Kolupaev, Yu.E., Karpets, Yu.V., Beschasniy, S.P., and Dmitriev, A.P., Gasotransmitters and their role in adaptive reactions of plant cells, Cytol. Genet., 2019, vol. 53, p. 392. https://doi.org/10.3103/S0095452719050098
Bai, X., Chen, J., Kong, X., Todd, C.D., Yang, Y., Hu, X., and Li, D.Z., Carbon monoxide enhances the chilling tolerance of recalcitrant Baccaurea ramiflora seeds via nitric oxide-mediated glutathione homeostasis, Free Radical Biol. Med., 2012, vol. 53, p. 710. https://doi.org/10.1016/j.freeradbiomed.2012.05.042
Cheng, T., Hu, L., Wang, P., Yang, X., Peng, Y., Lu, Y., Chen, J., and Shi, J., Carbon monoxide potentiates high temperature-induced nicotine biosynthesis in Tobacco, Int. J. Mol. Sci., 2018, vol. 19, p. e188. https://doi.org/10.3390/ijms19010188
Li, Z.-G. and Gu, S.-P., Hydrogen sulfide as a signal molecule in hematin-induced heat tolerance of tobacco cell suspension, Biol. Plant, 2016, vol. 60, p. 595. https://doi.org/10.1007/s10535-016-0612-8
Kolupaev, Yu.E., Shkliarevskyi, M.A., Karpets, Yu.V., Shvidenko, N.V., and Lugovaya, A.A., ROS-dependent induction of antioxidant system and heat resistance of wheat seedlings by hemin, Russ. J. Plant Physiol., 2021, vol. 68, p. 322. https://doi.org/10.1134/S102144372101009X
Chen, Y., Wang, M., Hu, L., Liao, W., Dawuda, M.M., and Li, C., Carbon monoxide is involved in hydrogen gas-induced adventitious root development in cucumber under simulated drought stress, Front. Plant Sci., 2017, vol. 8, p. 128. https://doi.org/10.3389/fpls.2017.00128
She, X.P. and Song, X.G., Carbon monoxide-induced stomatal closure involves generation of hydrogen peroxide in Vicia faba guard cells, J. Integr. Plant Biol., 2008, vol. 50, p. 1539. https://doi.org/10.1111/j.1744-7909.2008.00716.x
Ling, T., Zhang, B., Cui, W., Wu, M., Lin, J., Zhou, W., Huang, J., and Shen, W., Carbon monoxide mitigates salt-induced inhibition of root growth and suppresses programmed cell death in wheat primary roots by inhibiting superoxide anion overproduction, Plant Sci., 2009, vol. 177, p. 331. https://doi.org/10.1016/j.plantsci.2009.06.004
Verma, K., Dixit, S., Shekhawat, G.S., and Alam, A., Antioxidant activity of heme oxygenase 1 in Brassica juncea (L.) Czern. (Indian mustard) under salt stress, Turk. J. Biol., 2015, vol. 39, p. 540. https://doi.org/10.3906/biy-1501-28
Wei, M.-Y., Chao, Y.-Y., and Kao, C.H. NaCl-induced heme oxygenase in roots of rice seedlings is mediated through hydrogen peroxide, Plant Growth Regul., 2013, vol. 69, p. 209. https://doi.org/10.1007/s10725-012-9762-7
Mahawar, L. and Shekhawa, G.S., EsHO 1 mediated mitigation of NaCl induced oxidative stress and correlation between ROS, antioxidants and HO 1 in seedlings of Eruca sativa: underutilized oil yielding crop of arid region, Physiol. Mol. Biol. Plants, 2019, vol. 25, p. 895. https://doi.org/10.1007/s12298-019-00663-71
Yuan, X.X., Wang, J., Xie, Y.J., and Shen, W.B., Effects of carbon monoxide on salt tolerance and proline content of roots in wheat seedling, Plant Physiol. Commun., 2009, vol. 45, p. 567.
Zhang, C., Li, Y., Yuan, F., Hu, S., and He, P., Effects of hematin and carbon monoxide on the salinity stress responses of Cassia obtusifolia L. seeds and seedlings, Plant Soil, 2012, vol. 359, p. 85. https://doi.org/10.1007/s11104-012-1194-7
Xu, S., Sa, Z.-S., Cao, Z.-Y., Xuan, W., Huang, B.-K., Ling, T.-F., Hu, Q.-Y., and Shen, W.-B., Carbon monoxide alleviates wheat seed germination inhibition and counteracts lipid peroxidation mediated by salinity, J. Integr. Plant Biol., 2006, vol. 48, p. 1168. https://doi.org/10.1111/j.1744-7909.2006.00337.x
Shkliarevskyi, M.A., Kolupaev, Yu.E., Yastreb, T.O., Karpets, Yu.V., and Dmitriev, A.P., The effect of CO donor hemin on the antioxidant and osmoprotective systems state in Arabidopsis of a wild-type and mutants defective in jasmonate signaling under salt stress, Ukr. Biochem. J., 2021, vol. 93 (3), p. 39. https://doi.org/10.15407/ubj93.03.039
Wei, Y.Y., Zheng, Q., Liu, Z.P., and Yang, Z.M., Regulation of tolerance of Chlamydomonas reinhardtii to heavy metal toxicity by heme oxygenase-1 and carbon monoxide, Plant Cell Physiol., 2011, vol. 52, p. 1665. https://doi.org/10.1093/pcp/pcr102
Meng, D.K., Chen, J., and Yang, Z.M., Enhancement of tolerance of Indian mustard (Brassica juncea) to mercury by carbon monoxide, J. Hazard. Mater., 2011, vol. 186, p. 1823. https://doi.org/10.1016/j.jhazmat.2010.12.062
Chen, Q., Gong, C., Ju, X., Zhu, Z., Shen, W., Shen, Z., and Cui, J., Hemin through the heme oxygenase 1/ferrous iron, carbon monoxide system involved in zinc tolerance in Oryza sativa L., J. Plant Growth Regul., 2018, vol. 37, p. 947. https://doi.org/10.1007/s00344-018-9793-z
Zhang, S., Wang, Q., Guo, Y., Kang, L., and Yu, Y., Carbon monoxide enhances the resistance of jujube fruit against postharvest Alternaria rot, Postharvest Biol. Technol., 2020, vol. 168, art. ID 111268. https://doi.org/10.1016/j.postharvbio.2020.111268
He, H. and He, L., The role of carbon monoxide signaling in the responses of plants to abiotic stresses, Nitric Oxide, 2014, vol. 42, p. 40. https://doi.org/10.1016/j.niox.2014.08.011
Baudouin, E., The language of nitric oxide signaling, Plant Biol., 2011, vol. 13, p. 233. https://doi.org/10.1111/j.1438-8677.2010.00403.x
Kim, M.C., Chung, W.S., Yun, D., and Cho, M.J., Calcium and calmodulin-mediated regulation of gene expression in plants, Mol. Plant, 2009, vol. 2, p. 13. https://doi.org/10.1093/mp/ssn091
Bürstenbinder, K., Möller, B., Plötner, R., Stamm, G., Hause, G., Mitra, D., and Abel, S., The IQD family of calmodulin-binding proteins links calcium signaling to microtubules, membrane subdomains, and the nucleus, Plant Physiol., 2017, vol. 173, p. 1692. https://doi.org/10.1104/pp.16.01743
Medvedev, S.S., Principles of calcium signal generation and transduction in plant cells, Russ. J. Plant Physiol., 2018, vol. 65, p. 771. https://doi.org/10.1134/S1021443718060109
Wilkinson, W.J. and Kemp, P.J., Carbon monoxide: an emerging regulator of ion channels, J. Physiol., 2011, vol. 589, p. 3055. https://doi.org/10.1113/jphysiol.2011.206706
Neill, S., Barros, R., Bright, J., Desikan, R., Hancock, J., Harrison, J., Morris, P., Ribeiro, D., and Wilson, I., Nitric oxide, stomatal closure and abiotic stress, J. Exp. Bot., 2008, vol. 59, p. 165. https://doi.org/10.1093/jxb/erm293
Shkliarevskyi, M.A., Karpets, Yu.V., Kolupaev, Yu.E., Lugovaya, A.A., and Dmitriev, A.P., Calcium-dependent changes in cellular redox homeostasis and heat resistance of wheat plantlets under influence of hemin (carbon monoxide donor), Cytol. Genet., 2020, vol. 54, p. 522. https://doi.org/10.3103/S0095452720060109
Mukherjee, S. and Corpas, F.J., Crosstalk among hydrogen sulfide (H2S), nitric oxide (NO) and carbon monoxide (CO) in root-system development and its rhizosphere interactions: a gaseous interactome, Plant Physiol. Biochem., 2020, vol. 155, p. 800. https://doi.org/10.1016/j.plaphy.2020.08.020
Song, X.G., She, X.P., and Zhang, B., Carbon monoxide-induced stomatal closure in Vicia faba is dependent on nitric oxide synthesis, Physiol. Plant, 2008, vol. 132, p. 514. https://doi.org/10.1111/j.1399-3054.2007.01026.x
Shkliarevskyi, M.A., Kolupaev, Yu.E., Karpets, Yu.V., Lugovaya, A.A., and Bessonova, V.P., Involvement of nitrate reductase and nitric oxide (NO) in implementation of the stress-protective action of a carbon monoxide (CO) donor on wheat seedlings under hyperthermy, Russ. J. Plant Physiol., 2021, vol. 68, p. 688. https://doi.org/10.1134/S1021443721040166
Sane, P.V., Kumar, N., Baijal, M., Singh, K.K., and Kochhar, V.K., Activation of nitrate reductase by calcium and calmodulin, Phytochemistry, 1987, vol. 26, p. 1289. https://doi.org/10.1016/S0031-9422(00)81796-3
Gao, H., Jia, Y., Guo, S., Lv, G., Wang, T., and Juan, L., Exogenous calcium affects nitrogen metabolism in root-zone hypoxia-stressed muskmelon roots and enhances short-term hypoxia tolerance, J. Plant Physiol., 2011, vol. 168, p. 1217. https://doi.org/10.1016/j.jplph.2011.01.022
Gautam, V., Kaur, R., Kohli, S.K., Verma, V., Kaur, P., Singh, R., Saini, P., Arora, S., Thukral, A.K., Karpets, Yu.V., Kolupaev, Yu.E., and Bhardwaj, R., ROS compartmentalization in plant cells under abiotic stress condition, in Reactive Oxygen Species and Antioxidant Systems in Plants: Role and Regulation under Abiotic Stress, Khan, M.I.R. and Khan, N.A., Eds., Singapore: Springer-Verlag, 2017, p. 89. https://doi.org/10.1007/978-981-10-5254-5_4
Sharova, E.I. and Medvedev, S.S., Redox reactions in apoplast of growing cells, Russ. J. Plant Physiol., 2017, vol. 64, p. 1. https://doi.org/10.1134/S1021443717010149
Minibayeva, E.V., Gordon, L.K., Kolesnikov, O.P., and Chasov, A.V., Role of extracellular peroxidase in the superoxide production by wheat root cells, Protoplasma, 2001, vol. 217, p. 125. https://doi.org/10.1007/BF01289421
Kreslavski, V.D., Los, D.A., Allakhverdiev, S.I., and Kuznetsov, Vl.V., Signaling role of reactive oxygen species in plants under stress, Russ. J. Plant Physiol., 2012, vol. 59, p. 141. https://doi.org/10.1134/S1021443712020057
Mamaeva, A.S., Fomenkov, A.A., Nosov, A.V., Moshkov, I.E., Novikova, G.V., Mur, L.A.J., and Hall, M.A., Regulatory role of nitric oxide in plants, Russ. J. Plant Physiol., 2015, vol. 62, p. 427. https://doi.org/10.1134/S1021443715040135
Wang, Y.-Q., Liu, Y.-H., Wang, S., Du, H.-M., and Shen, W.-B., Hydrogen agronomy: research progress and prospects, J. Zhejiang Univ., Sci., B, 2020, vol. 21, p. 841. https://doi.org/10.1631/jzus.B2000386
Cao, Z., Huang, B., Wang, Q., Xuan, W., Ling, T., Zhang, B., Chen, X., Nie, L., and Shen, W., Involvement of carbon monoxide produced by heme oxygenase in ABA-induced stomatal closure in Vicia faba and its proposed signal transduction pathway, Chin. Sci. Bull., 2007, vol. 52, p. 2365. https://doi.org/10.1007/s11434-007-0358-y
Shan, C., Wang, T., Zhou, Y., and Wang, W., Hydrogen sulfide is involved in the regulation of ascorbate and glutathione metabolism by jasmonic acid in Arabidopsis thaliana, Biol. Plant, 2018, vol. 62, p. 188. https://doi.org/10.1007/s10535-017-0740-9
Ton, J., Flors, V., and Mauch-Mani, B., The multifaceted role of ABA in disease resistance, Trends Plant Sci., 2009, vol. 14, p. 310. https://doi.org/10.1016/j.tplants.2009.03.006
Yastreb, T.O., Kolupaev, Yu.E., Shkliarevskyi, M.A., and Dmitriev, A.P., Participation of jasmonate signaling components in the development of Arabidopsis thaliana’s salt resistance induced by H2S and NO donors, Russ. J. Plant Physiol., 2020, vol. 67, p. 827. https://doi.org/10.1134/S1021443720050192
Lamar, C.A., Mahesh, V.B., and Brann, D.W., Regulation of gonadotrophin-releasing hormone (GnRH) secretion by heme molecules: a regulatory role for carbon monoxide? Endocrinology, 1996, vol. 137, p. 790. https://doi.org/10.1210/endo.137.2.8593832
Landaw, S.A., Callahan, E.W., Jr., and Schmid, R., Catabolism of heme in vivo: comparison of the simultaneous production of bilirubin and carbon monoxide, J. Clin. Invest., 1970, vol. 49, p. 914. https://doi.org/10.1172/JCI106311
Ryter, S.W., Therapeutic potential of heme oxygenase-1 and carbon monoxide in acute organ injury, critical illness, and inflammatory disorders, Antioxidants, 2020, vol. 9, p. 1153. https://doi.org/10.3390/antiox9111153
Le, C.T.T., Brumbarova, T., and Bauer, P., The interplay of ROS and iron signaling in plants, in Redox Homeostasis in Plants: Signaling and Communication in Plants, Panda, S.K. and Yamamoto, Y.Y., Eds., Cham: Springer-Verlag, 2019, p. 43. https://doi.org/10.1007/978-3-319-95315-1_3
Sa, Z.S., Huang, L.Q., Wu, G.L., Ding, J.P., Chen, X.Y., Yu, T., Ci, S., and Shen, W.B., Carbon monoxide: a novel antioxidant against oxidative stress in wheat seedling leaves, J. Integr. Plant Biol., 2007, vol. 49, p. 638. https://doi.org/10.1111/j.1744-7909.2007.00461.x
Trchounian A., Petrosyan, M., and Sahakyan, N., Plant cell redox homeostasis and reactive oxygen species, in Redox State as a Central Regulator of Plant-Cell Stress Responses, Gupta, D.K., Palma, J.M., and Corpas, F.J., Eds., Cham: Springer-Verlag, 2016, p. 25. https://doi.org/10.1007/978-3-319-44081-1_2
Kolupaev, Yu.E., Yastreb, T.O., Oboznyi, A.I., Ryabchun, N.I., and Kirichenko, V.V., Constitutive and cold-induced resistance of rye and wheat seedlings to oxidative stress, Russ. J. Plant Physiol., 2016, vol. 63, p. 326. https://doi.org/10.1134/S1021443716030067
Magierowski, M., Magierowska, K., Hubalewska-Mazgaj, M., Sliwowski, Z., Ginter, G., Pajdo, R., Chmura, A., Kwiecien, S., and Brzozowski, T., Carbon monoxide released from its pharmacological donor, tricarbonyldichlororuthenium (II) dimer, accelerates the healing of pre-existing gastric ulcers., Br. J. Pharmacol., 2017, vol. 174, p. 3654. https://doi.org/10.1111/bph.13968
Beschasnyi, S.P. and Hasiuk, O.M., The effect of carbon monoxide’s donor CORM-2 on erythrocyte aquaporins, World Med. Biol., 2021, vol. 2, p. 167. https://doi.org/10.26724/2079-8334-2021-2-76-167-173
Adach, W. and Olas, B., Carbon monoxide and its donors—their implications for medicine, Future Med. Chem., 2019, vol. 11, p. 60. https://doi.org/10.4155/fmc-2018-0215
Adach, W., Błaszczyk, M., and Olas, B., Carbon monoxide and its donors—Chemical and biological properties, Chem.-Biol. Interact., 2020, vol. 318, art. ID 108973. https://doi.org/10.1016/j.cbi.2020.108973
Yuan, Z., Yang, X., and Wang, B., Redox and catalase-like activities of four widely used carbon monoxide releasing molecules (CORMs), Chem. Sci., 2021, vol. 12, art. ID 13013. https://doi.org/10.1039/D1SC03832J
Kolupaev, Yu.E. and Yastreb, T.O., Jasmonate signaling and plant adaptation to abiotic stressors (review), Appl. Biochem. Microbiol., 2021, vol. 57, p. 1. https://doi.org/10.1134/S0003683821010117
Corpas, F.J. and Palma, J.M., H2S signaling in plants and applications in agriculture, J. Adv. Res., 2020, vol. 24, p. 131. https://doi.org/10.1016/j.jare.2020.03.011
Singhal, R.K., Jatav, H.S., Aftab, T., Pandey, S., Mishra, U.N., Chauhan, J., Chand, S., Indu, Saha, D., Dadarwal, B.K., Chandra, K., Khan, M.A., Rajput, V.D., Minkina, T., Narayana, E.S., Sharma, M.K., et al., Roles of nitric oxide in conferring multiple abiotic stress tolerance in plants and crosstalk with other plant growth regulators, J. Plant Growth Regul., 2021, vol. 40, p. 2303. https://doi.org/10.1007/s00344-021-10446-8
ACKNOWLEDGMENTS
I am grateful to T.O. Yastreb for assistance in preparation of the illustrations.
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Abbreviations: 6-BAP—6-benzylaminopurine; BV—biliverdin; HO—heme oxygenase; PTIO—2-phenyl-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide; SOD—superoxide dismutase.
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Kolupaev, Y.E. Gasotransmitter Carbon Monoxide: Synthesis and Functions in Plants. Russ J Plant Physiol 69, 42 (2022). https://doi.org/10.1134/S1021443722030074
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DOI: https://doi.org/10.1134/S1021443722030074