Physiological Respon of Tpd-affected Rubber Plant to Growth
Regulator and Antioxidant Treatments
Ade Fipriani
1
, Rosmayati
2
, Radite Tistama
3
and Revandy I. M. Damanik
2
1
Doctoral Program of Agricultural Sciences, Faculty of Agriculture, Universitas Sumatera Utara, Padang Bulan, Medan,
Indonesia
2
Program study of Agrotechnology, Faculty of Agriculture, Universitas Sumatera Utara, Padang Bulan, Medan, Indonesia
3
Sugei Putih Research Centre, Rubber Research Institute, Sungei Putih, Deli Serdang, Indonesia
Keywords: Bark, Leaf Fall Session, Physiological Characters and Protein.
Abstract: The research aimed to determine bark and latex the effect of applied NAA on thiol content, total protein and
peroxidase activity in the bark and latex of TPD affected rubber tree (Hevea brasiliensis muell Arg.). The
research was conducted at the Sungei Putih Estate with 54 meters altitude, in leaf fall session from January
2018 to July 2018. The experiment was design using Split Plot Design, with three factors i.e: clones (RRIM
921 and PB 260), condition of plants (Healthy and TPD) and the formula (control, 2.5% and 5% the
stimulants). Parameter observed were thiol and protein content and peroxidase activity. The results showed
that the range of values bark and latex are Thiol 0.1-1.7 µM, Protein 31-124 ppm and Peroxidase 0,01- 0,9
unit/ppm protein, the clone of rubber plants was significantly affected the thiol’s. The NAA application
could improve the physiological characters of the rubber plant and the activities from all parameters
significantly affected by environmental conditions.
1 INTRODUCTION
Production of rubber plants with potential production
decreased reaching 114.74 kg / ha / t and 183.05 kg /
ha / year caused of Tapping Panel Dryness (TPD)
(Mochlisin & Tistama, 2014). In Indonesia, TPD
incident on productive rubber estate reach 20-50%,
which is characterized by the cessation of latex flow
and dryness for of the line of tapping. The economical
lossing caused by TPD incident are estimated to be
more than 1.7 billion/ year. Not balancing in latex
metabolism caused exploitation and the less
maintenance of plants are as mean factors inducing
TPD incident (Andryanto & Tistama 2014). Efforts to
limited incident are manuring, and restoration of
tapping fields for 6 months, with hormon application
and triadimephone 250 g/l (Sirait Syahnen, 2013).
However, TPD incident is still to be major problem in
Indonesian rubber plantations.
Physiological stress caused tapping in rubber tree
induces free radical compounds such as 0
2
-, H
2
0
2
,
OH*, QO* (Jacob, 1989). These reactive system
oxygen (ROS) enter into latex vessel cells (laticifer)
and interfere laticifer cell organels that are causing
cells disrupstion (Tistama, 2013). In TPD affected
plant, many genes related with a role in triggering
programmed cell death (PCD) were up regulated
during the early of TPD syndrome (Venkatachalam et
al. 2007).
Therefore, the earliest symptoms of histology
appearing in laticifer cells. So, it’s very likely to be
said that the trigger for a oxidative stress was known
in initially laticifer plants (Jacob and Krishnakumar,
2006). Joseph (2006) reported that the nutrient
content of P, Mg, and Mn in the latex is higher, while
Fe and Zn are lower in TPD-affected plant compared
to normal plants. Gebelin et al., (2013) said
detoxification of ROS by SOD, peroxidase and
catalase activity or through other non-enzymatic
mechanisms capable to detoxifying ROS from the
tissue without causing disrups. Thus, peroxidase and
catalase activities are key role in the process of
removing H
2
O
2
molecules in plant tissues.
Thiol in the plant tissue actives enzymes that have
control in respons to environmental stress conditions
as major antioxidace in the Hevea latex Zhang et al.
2017). Thiol levels are importance as indicatitor that
is related to the physiological susceptibility of latex,
especially in the incidence of TPD, and thiol status
shows of plants to the pressure of exploitation (Zhang
270
Fipriani, A., Rosmayati, ., Tistama, R. and Damanik, R.
Physiological Respon of Tpd-affected Rubber Plant to Growth Regulator and Antioxidant Treatments.
DOI: 10.5220/0008553002700274
In Proceedings of the International Conference on Natural Resources and Technology (ICONART 2019), pages 270-274
ISBN: 978-989-758-404-6
Copyright
c
2019 by SCITEPRESS Science and Technology Publications, Lda. All rights reserved
et al. 2017) The higher the intensity of exploitation
the lower the thiol level (Sumarmadji et al, 2004).
Sumarmadji and Tistama (2004) found thiol has the
ability to protect sub-cellular organelles and to cacth
the toxic oxygen molecules. This toxic oxygen
molecule causes exhaustion of latex vessel cells
which triggers TPD. The optimal content of thiol
ranges from 0.4 to 0.9 mM and the critical condition
is below 0.2 mm.
Peroxidase enzyme is one of the plant enzymes
that has a relationship with the process of resistance
(Zhang et al, 2017). According to Andrianto &
Tistama (2014) the difference in tolerance between
high and low metabolism of rubber clone is thought
to be due to the content of antioxidant compounds in
bark tissue and latex. To find out the sensitivity and
resistance of plants to disease attacks an approach is
used regarding the influence of environmental stress
on plant physiology processes. such as ethylene
treatment (Putranto et al. 2015).
Based on the early description, TPD is one of the
important problems that immediately need to be
resolved. The existence of leaf fall session can also
reduce the value of rubber production. Research on
rubber bark is needed cause the bark is where latex is
produced. Analysis of several physiological
parameters, is expected to be an early indicator of
healing process. These study aimed to increase the
cure rate of TPD by giving NAA formula and
Ascorbate acid and in the future it can reduce
production losses due to TPD and leaf fall session and
to examine changes in antioxidant compounds in
healthy and affected TPD plants with NAA and
ascorbic acid nutrition treatments.
2 MANUSCRIPT PREPARATION
2.1 Page Setup
Plant materials used for this study were PB 260 clones
(High metabolism) and RRIM 921 (Medium
metabolism) planted in 2006 with 3 x 6 m spacing.
The experiment was arranged with a Split-Split Plot
Design with three replications, each replication
consisting of 1 plant. The selection of the TPD
affected plants was carried out by cutting the tapping
panel with a tapping knife. Rubber plants are tapped
using a system tapping 1/2S d/3 (tapped every 3 days
with a length of 1/2 spiral of stem).
Formula for treatment in the form of minerals
follows the composition of Murashige & Skoog (MS)
with the addition of NAA (100 ppm, and ascorbic
acid (150 ppm). The solution was spryed on tapping
panel every 15 days for 3 month with a dose of 5 ml /
tree. Latex samples were collected into steril tube,
while bark samples were taken by cork borer
(diameter 1 cm) at 5 cm under tapping line, then
carrying in the box ice to laboratory.
2.2 Protein Extraction and Peroxidase
Activity
According to Bradford (1976), protein extraction for
lateks was perfomed by ten ml of each latex samples
were centrifuged at 15000 rpm for 20 min at
temperatur 4
O
C. Clear phase was transfered into the
new tube and used to protein and enzyme analysis.
Protein extraction for bark was performed following
of procedure Packeer-Mohamad et al. (2012). The
soft tissue of bark (3-4 mm from cambium) was
ground with liquid nitrogen and extracted in 0.2 M
phosphate buffer, pH 6.5, containing 0.25% (v/v)
Triton X-100 and 3% (w/v) polyvinylpyrrolidone
(PVPP). Bark samples were frozen in liquid nitrogen
and grinded in the mortar. One gram of bark powders
were extracted with phosphate bufer pH 7,2 using
vortex for five minutes. The extracts were centrifuged
at 12000 rpm in 4
O
C for 15 minute. Supernatan was
tranfered to new tube and ready for enzymatic
analysis. peroxidase activity uses phenol-
aminoantipirine A solution (phenol 810 mg solution
and amino antiphirine 25 mg in 50 ml water) and
solution B by mixing 30% H2O2 added with MES
Buffer solution pH 6 measured at 510 nm absorbance
(Shannon et al., 1996).
2.3 Physiological Analysis
For bark physiological analysis, one gram powder
was extracted in TCA 5% solution, then suspension
was centrifugated 10000 rpm for 15 minute. Analysis
of thiol content was based on the principle of its
reaction with dithiobis-nitrobenzoate acid (DTNB) to
form a yellow TNB absorbed at λ 421 nm
(nanometer) with a Beckman spectrophotometer DU
650 (Bobbiliof, 1923). Thiol indicated the level of
lutoids protection and the stability of latex. Thiol
contents were expressed in millimoles per liter of
latex (mmol.g
-1
).
2.4 Statistic Test
The results were tested by ANOVA and for the
treatment effect will be continued with Tukey
Multiple Comparison at alpha = 5%. Correlation
Physiological Respon of Tpd-affected Rubber Plant to Growth Regulator and Antioxidant Treatments
271
between parameters was tested Pearson Correlation
analysis using Minitab version 16 sofware.
3 RESULT AND DISCUSSION
3.1 Result
The latex thiol content in the both of rubber clone
(Figure 3) were lower in TPD affected plant than
health plants. PB 260 was higher thiol content both
in health or TPD partial than that of RRIM 921. In
leaf fall condition, latex thiol contents were 2-5 times
higher than full leaf condition. The thiol content was
decrease in health clones after the trees were treated
with ethepon. In TPD affected plants of PB 260, the
thiol content was categorized high and its was not
affected by ethepon treatments.In full leaf condition,
the thiol contents was normally in all of plant healthy
condition even in the plants treating with ethepon.
Generally, thiol content in bark of TPD affected
plant the RRIM 912 was higher than that of healthy
plants in March. The thiol content decrease in bark
of this clone after treating with ethepon 2,5% and
then increase with ethepon 5% treatment. In leaf
fall condition PB 260 has diference pattern in its
response to ethepon. Thiol bark content in May was
relatively flate by ethepon treatment.
3.2 Discussion
Latex POD activity was affected significantly by leaf
condition, ethepon treatment and clone. POD activity
in the bark PB 260 in full leaf periode was very high
in health plant, and the activity sharly reduced by
ethepone treatments. The bark high peroxidase
activity was negatively correlation with TPD level
(Tistama et al. 2019). The level of POD activity was
decrease by The health rubber tree could be indicated
by high POD activity in the latex and bark both in low
or high metabolism clone, however the level of POD
activity should be classified based on level of
physiology healthy. Opponent with POD activity, the
thiol content in March or in fall leaf condition. In May
when the leaf is full the thiol content decreased both
in the latex and bark. The thiol is dominan in thefall
leaf stress, while POD is dominan in ethephon
treatment.
(A)
(B)
Figure 1: Thiol content (mM) in health and TPD affected plant of the RRIM 912 and PB 260 latex (A= March and B = May).
(A)
(B)
Figure 2: Thiol content (mM) in the bark of health and TPD partial plant in March and May. (A= March and B = May).
ICONART 2019 - International Conference on Natural Resources and Technology
272
The content formulas shows the association of
formulas in improving of stress tolerance plants
through formulas supporting the performance of POD
in the detoxification process with both enzymatic and
non-enzymatic reactions. Although ethrel treatment
increases physiological stress in rubber plants due to
tissue injury which causes the sink and source process
to be unbalance. By combining ethrel and 100 ppm
and 150 ascorbic acid formulas as if to provide injury
and healing at the same time so that even though they
are still able to increase latex POD activity it is proven
by lower control plants in March observations with
the highest content below 0.3 units / ppm compared
to ethrel and formula which reached more than 0.4
units / ppm. This is presumably because of the
ascorbic acid content which acts as an antioxidant so
that it can support the role of peroxidase in the process
of removing ROS molecules such as H
2
O
2
. Winarsih
(2000) mention the main target of ROS is protein,
unsaturated fatty acids and lipoproteins, and DNA
elements including carbohydrates and RNA.
Unsaturated fatty acids are the most vulnerable to
ROS attacks. Ardiansyah et al. (2014) said ascorbic
acid functions as an antioxidant, cofactor enzyme and
as a cell signal modulator in a variety of important
physiological processes, including cell wall
biosynthesis, secondary metabolites and
phytohormones, stress tolerance, photoprotection,
cell division and growth.
The control plants there was an increase in the
content of POD which was very drastically observed
in May compared to March, this is thought to be
related to the deciduous process of leave fall session,
where May is the beginning of re-formation of
leaves so that the plants are no longer in stress.
Gunasekara et al., (2013) said that there were
differences in the production and response of each
clone to the seasonal pattern. The results showed that
PB260 clone activity looked more stable towards
changes in seasonal patterns compared to RRIM 912
clones which showed a very drastic difference. This
is in accordance with Siregar's statement (2016) PB
260 prioritizes thiol function in controlling stress
while in low metabolic plants prioritizes POD
enzymes. Siregar (2014) also said that canopy in
PB260 is generally thicker and thicker concentrating
on the number of fallers more and has a fast response
to changes in rainfall. This is related to the
hypersensitivity resistance gene that is dominantly
expressed in plants, the gene encoding peroxidee
enzyme and polyphenol peroxidase. Both of these
enzymes more commonly play a role in defense
mechanisms against diseases so that their activities
are used as resistance induction (Saravanan et al.,
2004).
Thiol contents in latex generally will increase if
the plant is exposed by TPD and given stimulants,
especially in PB260 plants. However, for healthy
plants the content will decrease. This happens
related to the level of exploitation and metabolism of
each clone. Research by Sumarmadji (2000) says
that the analysis of latex content in partial TPD
plants is known to show low thiol content even
though the plants were given stimulants ethepon and
Tistama et. Al (2006) which stated that thiol and
ATP in healthy plants were higher than those
attacked by TPD. This is thought to be an attempt by
the plant to overcome the conditions of oxidative
stress stress. According to Anggraini (2016), PB260
is more susceptible to attack by TPD.
Higher thiol content in PB260 bark compared to
RRIM 921 clones showed quick stater clones to
experience higher exploitation than slow stater. This
is an indication that slow stater plants are more
tolerant of TPD. The higher thiol content of the bark
can also indicate the presence of TPD whereas in
healthy plants the content of thiol bark is lower even
though it has been given stimulants up to 5% this is
because the plants give a better response to stimulants
combined with 100 ppm NAA formula and Ascorbic
Acid 150 ppm (Figure 4). Siregar et al., (2008)
reported that quick starter clones have a characteristic
that is the peak pattern of latex production occurs in
the early period, stimulant responsiveness,
susceptible to TPD and thin skin recovery, while slow
starter clones reach peak production in the middle of
tapping period, stimulant response, relatively
resistant to over-exploitation and thick skin recovery.
4 CONCLUSIONS
The Difference of antioxidant activities in the bark
and latex rubber plants (Hevea brasiliensis) change
according to environmental factors, clones, and
physiological disorders in this case because of the
provision of stimulants and nutrients and ascorbic
acid. Increasing the value of thiol can reduce the
value of protein and POD activity. Some parameters
that can be used as early indicators for detecting TPD
are bark POD activity and thiol latex value and based
on observations in the field of using 100 ppm NAA
formulas and Askorbit Acid 150 ppm can reduce the
level of TPD in rubber plants. From the results of this
study it is recommended to further investigate the
metabolism of rubber plant bark and its formulas in a
longer period of at least 6 months to 12 months.
Physiological Respon of Tpd-affected Rubber Plant to Growth Regulator and Antioxidant Treatments
273
ACKNOWLEDGEMENTS
These research was funded by the Ministry of
Research and Technology of Higher Education,
Lecturer Dissertation Research Scheme Fiscal Year
2018. Thank you also to all promoter and my family
for their moral support and all the friends who helped
this research.
REFERENCES
Anggraini, U. 2016. Aktivitas Superoksida Dismutase
(SOD) dan fisiologi lateks pada Tanaman karet (Hevea
brasiliensis Muell arg.) PB260 dan RIM 921 Kering
Alur Sadap (KAS) Parsial dengan Pemberian Zat
Pengatur Tumbuh. Skripsi, USU, Medan
Andriyanto, M., Tistama, R. 2014. Perkembangan dan
Upaya Pengendalian Kering Alur Sadap (KAS) pada
Tanaman Karet (Hevea brasiliensis. Warta Perkaretan,
33(2); 2014.
Ardiansyah, M., Mawarni, L., Rahmawati, N. 2014. Respon
Pertumbuhan dan Produksi Kedelai Hasil Seleksi
Terhadap Pemberian Asam Askorbat dan Inokulasi
Fungi Mikoriza Arbuskukar di Tanah Salin. Universitas
Sumatera Utara. Medan.
Bobbiliof, W. 1923. Anatomy and physiology of Hevea
brasiliensis. Institute Orell Fussli, Zurich
Bradford, MM. 1976. A rapid and sensitive method for the
quantitation of microgram quantities of protein
utilissing the principle of the protein. Analytical
biochemistry, 72, 248-254.
Gebelin V., Leclercq, J., Hu. S., Tang C., Montoro P. 2013.
Regulation of MIR Genes in Response to Abiotic Stress
in Hevea brasiliensis International Journal of
Molecular Sciences 14(10), 1422-0067
Imelda, M., Estiati, A., Hartati, N. S. 2001. Induction of
Mutation through GaµMa Irradition in three Cultivars
of Banana. J. Annalaes Bogorienses. 7 (2): 75-82
Mochlisin, A., Tistama, R. 2014. Perkembangan dan Upaya
Pengendalian Kering Alur Sadap (KAS) Pada Tanaman
Karet (Hevea brasiliensis). Warta Perkaretan 33 (2),
89-102
Saravanan, T., Bhaskaran, R., Muthusamy, M. 2004.
Pseudomonas fluorescens Induced Enzymological
Changes in Banana Roots. J. Pant Pathology. 3 (2): 72-
80
Sirait, D. D. N., Syahnen. 2013. Pengembangan Dan
Aplikasi Teknologi Pengendalian Penyakit Kering Alur
Sadap (KAS) Pada Tanaman Karet Di Propinsi
Sumatera Selatan. Balai Besar Perbenihan dan Proteksi
Tanaman Perkebunan (BBP2TP), Medan
Siregar, T. H. S. 2014. Pola Musiman Produksi Dan Gugur
Daun Pada Klon PB 260 dan RRIC 100. J. Penelitian
Karet. 32 (2): 88-97
Siregar, T. H. S., Junaidi, Sumarmadji, N. Siagian, Karyudi.
2008. Perkembangan Penerapan Rekomendasi Sistem
Eksploitasi Tanaman Karet di Perusahaan Besar
Negara. Prosiding Lokakarya Nasional Agribisnis
Karet 2008. Yogyakarta, 217-232
Siregar, M. P. A. 2016. Aktivitas Enzim Peroksidase (Pod)
Lateks Dan Analisis Fisiologi Kulit Karet (Hevea
Brasiliensis Muell. Arg) Klon Pb 260 Dan Rrim 921
Dengan Pemberian Antidepresan Pada Musim Gugur
Daun. Skripsi. USU, Medan
Sumarmadji. 2000. Sistem Eksploitasi Tanaman Karet
Yang Spesifik Diskriminatif. Warta Pusat Penelitian
Karet, 19 (1-3), 31-39.
Sumarmadji, Siswanto, Yahya, S. 2004. Penggunaan
parameter fisiologi lateks untuk penentuan sistem
eksploitasi tanaman karet. J. Penelitian Karet.
22(1):41-52.
Sumarmadji, Tistama, R. 2004. Deskripsi Klon Karet
Berdasarkan Karakter Fisiologi Lateks Untuk
Menetapkan Sistem Eksploitasi Yang sesuai. Jurnal
Penelitian Karet, 22(1): 27 40
Steel, R. G. D., Torrie J. H. 1995. Prinsip dan Prosedur
Statistika. Suatu pendekatan biometrik. Gramedia
Pustaka Utama. Jakarta.
Tistama, R. 2013. Faktor Histologis dan Fisiologis yang
Berkaitan dengan Produksi Lateks. Workshop
Eksploitasi Tanaman Karet Menuju Produktivitas
Tinggi dan Umur Ekonomis Optimal
Tistama, R., Sumarmadji, dan Siswanto. 2006. Kejadian
Kering Alur Sadap (KAS) dan Teknik Pemulihannya
Pada Tanaman Karet. In Prosiding Lokakarya Nasional
Budidaya Tanaman Karet, 274 285.
Winarsih, S. P. 2000. Pengaruh Zat Pengatur Tumbuh
Terhadap Pembentukan dan Pengakaran Tunas Mikro
pada Asparagus secara In Vitro. Jurnal Hort. 10. 1:11-
17.
Zhang Y, Leclercq, J., Montoro, P. 2017. Reactive oxygen
species in Hevea brasiliensis latex and relevance to
Tapping Panel Dryness. Tree Physiol. 37: 261269
Putranto R.A., Herlinawati, E., Rio, M., Leclercq, J.,.
Piyatrakul, P., Gohet, E., Sanier, C., Oktavia, F.,
Pirrello, J., Kuswanhadi, Montoro, P. 2015.
Involvement of Ethylene in the Latex Metabolism and
Tapping Panel Dryness of Hevea brasiliensis. Int. J.
Mol. Sci. 16: 17885-17908; doi:10.3390/
ijms160817885
ICONART 2019 - International Conference on Natural Resources and Technology
274