The DOI matches its Crossref record; 47 of the 47 references it cites were found in a registry or an index.
Evaluation of the stress‐inducible production of proline in transgenic sugarcane (Saccharum spp.): osmotic adjustment, chlorophyll fluorescence and oxidative stress
Abstract
Proline accumulates in a variety of plant species in response to stresses such as drought, salinity and extreme temperatures. Although its role in plant osmotolerance remains controversial, proline is thought to contribute to osmotic adjustment, detoxification of reactive oxygen species and protection of membrane integrity. In the present study, we evaluated the effects of stress‐inducible proline production on osmotic adjustment, chlorophyll fluorescence and oxidative stress protection in transgenic sugarcane transformed with a heterologous P5CS gene. In well‐watered conditions, free proline, malondialdehyde (MDA) levels, Fv/Fm ratios and chlorophyll contents (Chls) in transgenic sugarcane were not statistically different from non‐transformed control plants. After 9 days without irrigation, proline content in transgenic events was on the average 2.5‐fold higher than in controls. However, no osmotic adjustment was observed in plants overproducing proline during the water‐deficit period. The photochemical efficiency of PSII observed was higher (65%) in the transgenic events at the end of the water‐deficit experiment. The effects of proline on lipid peroxidation as MDA levels and on the decline of Chl in paraquat‐treated leaf discs along the drought period suggest that proline protected the plants against the oxidative stress caused by the water deficit. The overall capacity of transgenic plants to tolerate water‐deficit stress could be assessed by the significantly higher biomass yields 12 days after withholding water. These results suggest that stress‐inducible proline accumulation in transgenic sugarcane plants under water‐deficit stress acts as a component of antioxidative defense system rather than as an osmotic adjustment mediator.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue Cultures
Murashige, T., & Skoog, F. (1962) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1962.tb08052.x · Cited by 67,392
Rapid determination of free proline for water-stress studies
Bates, L. S., Waldren, R. P., & Teare, I. D. (1973) · Plant and Soil · doi:10.1007/bf00018060 · Cited by 20,967
[34] Chlorophylls and carotenoids: Pigments of photosynthetic biomembranes
Lichtenthaler, H. K. (1987) · Methods in Enzymology · doi:10.1016/0076-6879(87)48036-1 · Cited by 13,616
Reactive oxygen species: Metabolism, oxidative stress, and signal transduction
Apel, K., & Hirt, H. (2004) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.55.031903.141701 · Cited by 11,723
Electromagnetic determination of soil water content: Measurements in coaxial transmission lines
Topp, G. C., Davis, J. L., & Annan, A. P. (1980) · Water Resources Research · doi:10.1029/wr016i003p00574 · Cited by 5,330
Roles of glycine betaine and proline in improving plant abiotic stress resistance
Ashraf, M., & Foolad, M. R. (2007) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2005.12.006 · Cited by 4,776
Hodges, D. M., DeLong, J. M., Forney, C. F., & Prange, R. K. (1999) · Planta · doi:10.1007/s004250050524 · Cited by 4,236
Asada, K. (1999) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.50.1.601 · Cited by 4,061
Cellular defenses against damage from reactive oxygen species
Yu, B. P. (1994) · Physiological Reviews · doi:10.1152/physrev.1994.74.1.139 · Cited by 2,370
Drought-induced responses of photosynthesis and antioxidant metabolism in higher plants
Reddy, A. R., Chaitanya, K. V., & Vivekanandan, M. (2004) · Journal of Plant Physiology · doi:10.1016/j.jplph.2004.01.013 · Cited by 2,327
Cited by
Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants
Gill, S. S., & Tuteja, N. (2010) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2010.08.016 · Cited by 11,663
Reactive oxygen species homeostasis and signalling during drought and salinity stresses
MILLER, G., SUZUKI, N., CIFTCI‐YILMAZ, S., & MITTLER, R. (2010) · Plant, Cell & Environment · doi:10.1111/j.1365-3040.2009.02041.x · Cited by 3,945
Abid, M., Ali, S., Qi, L. K., Zahoor, R., Tian, Z., Jiang, D., Snider, J. L., & Dai, T. (2018) · Scientific Reports · doi:10.1038/s41598-018-21441-7 · Cited by 567
Glycinebetaine and abiotic stress tolerance in plants
Giri, J. (2011) · Plant Signaling & Behavior · doi:10.4161/psb.6.11.17801 · Cited by 397
Nxele, X., Klein, A., & Ndimba, B. K. (2017) · South African Journal of Botany · doi:10.1016/j.sajb.2016.11.003 · Cited by 371
Metadata
- Authors
- Molinari, H. B. C., Marur, C. J., Daros, E., De Campos, M. K. F., De Carvalho, J. F. R. P., Filho, J. C. B., Pereira, L. F. P., & Vieira, L. G. E.
- Venue
- Physiologia Plantarum
- Publisher
- Wiley
- Published
- 2007-04-18
- Volume
- 130
- Issue
- 2
- Pages
- 218-229
- ISSN
- 0031-9317 (ISSN-L)
- 1399-3054
- OpenAlex
- W2016157570
- Cited by
- 370
- References
- 47
- FWCI
- 11.94
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Evaluation of the stress‐inducible production of proline in transgenic sugarcane (Saccharum spp.): osmotic adjustment, chlorophyll fluorescence and oxidative stress. https://app.cochat.ai/papers/10.1111/j.1399-3054.2007.00909.x
- The paper
- Molinari, H. B. C., Marur, C. J., Daros, E., De Campos, M. K. F., De Carvalho, J. F. R. P., Filho, J. C. B., Pereira, L. F. P., & Vieira, L. G. E. (2007). Evaluation of the stress‐inducible production of proline in transgenic sugarcane (Saccharum spp.): osmotic adjustment, chlorophyll fluorescence and oxidative stress. Physiologia Plantarum. https://doi.org/10.1111/j.1399-3054.2007.00909.x
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.