<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">AJPS</journal-id><journal-title-group><journal-title>American Journal of Plant Sciences</journal-title></journal-title-group><issn pub-type="epub">2158-2742</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ajps.2023.147049</article-id><article-id pub-id-type="publisher-id">AJPS-126436</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject></subj-group></article-categories><title-group><article-title>
 
 
  A Review of Main Factors Involved in the Maturation of Oil Palm (&lt;i&gt;Elaeis guineensis&lt;/i&gt; Jacq.) Fruit Bunches
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ngombo</surname><given-names>Clément Eya’a</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mva</surname><given-names>Armand Nsimi</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Pembe</surname><given-names>Hannah Ndele</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Bille</surname><given-names>Hermine Ngalle</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Thiery</surname><given-names>Molo</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Nkoulou</surname><given-names>Luther Fort Mbo</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Akoa</surname><given-names>Fouman</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Li-Gue</surname><given-names>Benoit Likeng</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ebongue</surname><given-names>Georges Frank Ngando</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Joseph</surname><given-names>Martin Bell</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Plant Biology and Physiology, Faculty of Sciences, University of Yaounde I, Yaounde, Cameroon</addr-line></aff><aff id="aff2"><addr-line>Institute of Agricultural Research for Development, Specialized Station for Oil Palm Research of La Dibamba, Douala, Cameroon</addr-line></aff><aff id="aff3"><addr-line>Plant Production Unit, Mbalmayo Agricultural Research Center (CRAM), Institute of Agricultural Research for Development, Mbalmayo, Cameroon</addr-line></aff><pub-date pub-type="epub"><day>19</day><month>07</month><year>2023</year></pub-date><volume>14</volume><issue>07</issue><fpage>727</fpage><lpage>740</lpage><history><date date-type="received"><day>1,</day>	<month>April</month>	<year>2023</year></date><date date-type="rev-recd"><day>17,</day>	<month>July</month>	<year>2023</year>	</date><date date-type="accepted"><day>20,</day>	<month>July</month>	<year>2023</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  The oil palm (
  Elaeis guineensis Jacq.) is a diploid perennial plant of the Arecaceae family. It is the most important plant cultivated for oil production. To ensure this production, certain optimal conditions are required: temperature, sunshine, rainfall, etc. The oil palm ensures its survival through the fruits borne on bunches located at the axis of the 17th to 20th leaves from the central stem. From pollination to the maturity of a bunch it takes about 4.5 to 6 months. Several events occur during this period: seed enlargement, weight increase, colour change, etc., but also important physiological changes: synthesis of some pigments (anthocyanin), increase in oil content correlated with the decrease in water content, etc. All of these constitute factors that can provide a better understanding of the biology of the seed. The aim of this work was to review some of the important parameters involved in the development and maturation of oil palm fruit bunches. These factors are classified into physiological, biochemical as well as environmental. The physiological parameters are color, appearance of embryo, seed weight and fruit detachment from bunches; Biochemical parameters include water content, oil content, carbohydrate, protein, mineral contents and lipase activity while temperature is the main environmental factor that affects fruit maturation. Thorough research has not yet been done at the different stages of maturation and ripening, thus a deep look into this may open up new avenues for research on early germinated oil palm seed production prior to seed dormancy.
 
</p></abstract><kwd-group><kwd>Oil Palm</kwd><kwd> Fruit Bunch</kwd><kwd> Germination</kwd><kwd> Maturation Parameters</kwd><kwd> Immature Seed</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Oil palm (Elaeis guineensis Jacq.) is a diploid perennial plant of the Arecaceae family. Currently, it is the most important crop in terms of oil production, which was estimated at about 72,940 (&#215;1000 MT) in 2019 [<xref ref-type="bibr" rid="scirp.126436-ref1">1</xref>] . This huge oil production is mainly due to average high yields compared to other oil crops. Favourable soil and climatic conditions for flourishing are fulfilled with a temperature of 25˚C - 28˚C, sunshine of at least 5 hours per day, rainfall between 1800 - 2400 mm/year and no continuous drought for more than 90 days. Oil palm prefers rich, well-drained soils, but grows well in poor soils if fertilized [<xref ref-type="bibr" rid="scirp.126436-ref2">2</xref>] , low altitude, ideally below 500 m [<xref ref-type="bibr" rid="scirp.126436-ref2">2</xref>] . The oil palm ensures its survival through its fruits borne by the female inflorescence. The female inflorescence is located in the axils of the 17th to 20th leaves from the central stem. The fruits are contained in bunches. The production of palm bunches is influenced by several factors including: nutrients, water, carbohydrate supply and pollination [<xref ref-type="bibr" rid="scirp.126436-ref3">3</xref>] . Changes in any of these factors may affect the level of production of fruit bunches. Of these factors, pollination has the greatest influence on palm bunch production. Poor pollination or inefficient pollination activity, separately or in combination, will lead to a low production of bunches [<xref ref-type="bibr" rid="scirp.126436-ref3">3</xref>] . The weight of palm bunches increases with age, with an average of 5 kg on 3 years old palms, and more than 25 kg for palms over 15 years of age [<xref ref-type="bibr" rid="scirp.126436-ref4">4</xref>] . It is also relevant to notice that the number of bunches produced per year per palm decreases with age, with a constant average weight compensated by an increase of the weigh of bunches. Moreover, the weight of a bunch depends partly on the fruit set and thus also on the efficiency of pollination [<xref ref-type="bibr" rid="scirp.126436-ref5">5</xref>] . From pollination to the maturity of a bunch it takes about 4.5 to 6 months [<xref ref-type="bibr" rid="scirp.126436-ref5">5</xref>] . Several events occur during this timeframe: seed enlargement, weight increase, colour change, etc. All of these constitute bunch maturation factors that can provide a better understanding of the biology of the seed, the average duration of bunch maturation period, and the changes in oil content and can as well open up new possibilities for seed production using innovative methods that are faster and less costly, particularly the germination of seeds before they enter the dormancy phase. The aim of this work was therefore to identify the biochemical, physiological and Environmental parameters involved in the development and maturation of an oil palm bunch.</p></sec><sec id="s2"><title>2. Anatomical and Physiological Level</title><sec id="s2_1"><title>2.1. Evolution of the Endosperm</title><p>The endosperm is the plant tissue where nutrient reserves in the seed of gymnosperms are stored. During the early phases of growth initiation in the oil palm, the endosperm is in a liquid form [<xref ref-type="bibr" rid="scirp.126436-ref6">6</xref>] . This liquid consistency corresponds to the coenocytic phase of the formation of this nuclear-like organ [<xref ref-type="bibr" rid="scirp.126436-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.126436-ref8">8</xref>] , which lasts until 56 Days after Pollination (DAP). After 70 DAP this tissue starts to become gelatinous. Several events take place in an increasing chronology during the process of endosperm development. Thus, the endosperm is present from 17 DAP. It is in a liquid form until 42 DAP. Between 42 and 70 DAP, it becomes gelatinous (<xref ref-type="fig" rid="fig1">Figure 1</xref> and <xref ref-type="fig" rid="fig2">Figure 2</xref>). At 84 DAP, it is cartilaginous and by 126 DAP, it has already acquired the final solid consistency of a mature endosperm [<xref ref-type="bibr" rid="scirp.126436-ref9">9</xref>] . This evolution coincides with the cessation of growth of the diameter of the seed coat which is thought to be associated with the accumulation of lipid reserves [<xref ref-type="bibr" rid="scirp.126436-ref9">9</xref>] . A similar evolution is described by [<xref ref-type="bibr" rid="scirp.126436-ref10">10</xref>] , where two weeks after pollination, the endosperm retains its liquid form. At the beginning of the 8th Week after Pollination (WAP), it increases in size and retains its liquid form. At 10 WAP the endosperm becomes semi-gelatinous. At the 12th week, lipogenesis starts and is almost complete at the 16th WAP. After the 16th WAP the endosperm starts to solidify [<xref ref-type="bibr" rid="scirp.126436-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.126436-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.126436-ref11">11</xref>] .</p></sec><sec id="s2_2"><title>2.2. Evolution of Seed Cavities</title><p>During the first 28 DAP, the average diameter of the seed coat does not exceed 1.80 mm [<xref ref-type="bibr" rid="scirp.126436-ref9">9</xref>] . It grows exponentially after 42 DAP and stabilizes after 98 days until full maturity at 168 DAP to reach 10.07 mm (<xref ref-type="fig" rid="fig3">Figure 3</xref>).</p></sec><sec id="s2_3"><title>2.3. Evolution of the Embryo</title><p>The differentiation of the embryo takes place between 60 and 70 DAP, a period during which the fruit develops to near maximum size [<xref ref-type="bibr" rid="scirp.126436-ref13">13</xref>] . Morphologically, it appears as a small cylindro-conical peg, which at maturity is about 3 mm long with a circumference of 1.2 mm, [<xref ref-type="bibr" rid="scirp.126436-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.126436-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.126436-ref15">15</xref>] , and embedded in the endosperm near the apex of the nucleus [<xref ref-type="bibr" rid="scirp.126436-ref16">16</xref>] . Full maturity arises between 70 and 80 DAP [<xref ref-type="bibr" rid="scirp.126436-ref5">5</xref>] and is followed by dormancy [<xref ref-type="bibr" rid="scirp.126436-ref17">17</xref>] .</p></sec><sec id="s2_4"><title>2.4. Evolution of the Endocarp</title><p>The endocarp refers to the innermost layer of the pericarp, the tissue of the fruit covering the seed. Tissue development begins during the first 70 DAP. This results in an exponential increase in its thickness. In the early stages of seed development, this tissue exhibits a whitish color. During the ripening phase of the fruit, the dehydration of this tissue continues accompanied by its hardening and color change [<xref ref-type="bibr" rid="scirp.126436-ref18">18</xref>] , with an outflow of P, K, Ca, and Mg. This is done such that at the end of the development of the fruit of E. guineensis, the endocarp is completely sclerified and has minimum water content. This dehydration begins from 10 WAP and will continue until the maturity of the fruit. Through this evolution, the endocarp progressively isolates and thus protects the seed from the rest of the fruit.</p></sec><sec id="s2_5"><title>2.5. Mesocarp Evolution</title><p>During the first 10 WAP, the growth of the parenchymal cells of the ovary wall is thought to be related to the presence of a large amount of water in this tissue [<xref ref-type="bibr" rid="scirp.126436-ref19">19</xref>] . Indeed, during this phase the mesocarp is continuously waterlogged and has a whitish color. Several physiological activities take place in this tissue, which would contribute to its elongation and stretching [<xref ref-type="bibr" rid="scirp.126436-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.126436-ref19">19</xref>] [<xref ref-type="bibr" rid="scirp.126436-ref20">20</xref>] , thus increasing its thickness. At this stage, lipids are practically non-existent. They start to be present from the 56th DAP, which would probably represent cellular and protoplasmic lipids contained in the mesocarp [<xref ref-type="bibr" rid="scirp.126436-ref19">19</xref>] . During this phase the mesocarp gradually turns yellow, which is indicative of the presence of lipids.</p></sec><sec id="s2_6"><title>2.6. Change in Color of the Fruits</title><p>This is the most important parameter. Classification according to color is based on certain principles. Before maturity in “nigrescens” form (the most common) the fruit is dark black at the base and orange at the top, and black after maturity (<xref ref-type="fig" rid="fig4">Figure 4</xref>), whereas in “virescens” form the fruit is green before maturity and at</p><p>maturity the color becomes entirely orange-green [<xref ref-type="bibr" rid="scirp.126436-ref22">22</xref>] . One of the first observations indicating the maturity of a bunch is the color change noticed on the fruits [<xref ref-type="bibr" rid="scirp.126436-ref5">5</xref>] . This color change is due to the presence of certain pigments (anthocyanin) lodged in the mesocarp. The mesocarp becomes increasingly orange as carotenoids are synthesized. [<xref ref-type="bibr" rid="scirp.126436-ref23">23</xref>] reported a 5-fold increase in carotenoid content between 105 and 140 (DAP).</p></sec></sec><sec id="s3"><title>3. Increase in Seed Weight</title><p>Increase in seed weight is a function of seed development, and is due to cell divisions and rapid expansion accompanied by a gradual accumulation of reserves. [<xref ref-type="bibr" rid="scirp.126436-ref6">6</xref>] and [<xref ref-type="bibr" rid="scirp.126436-ref10">10</xref>] have provided more details describing the development of a seed. For these authors, the fruits develop in size and weight, up to the 100th DAP, and also in dry matter weight. The same observation is made for other species of the plant kingdom such as soybean and maize [<xref ref-type="bibr" rid="scirp.126436-ref24">24</xref>] . In addition to cell division, lipid accumulation in the seed, evolution of the mesocarp and endosperm are closely related to weight increase [<xref ref-type="bibr" rid="scirp.126436-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.126436-ref19">19</xref>] (<xref ref-type="fig" rid="fig5">Figure 5</xref>).</p></sec><sec id="s4"><title>4. Fruit Ripening</title>Fruit Detachment from Bunches<p>This is characterized by the abscission of fruits from the bunch. It occurs first in the central part where the fruit is attached to the bunch. The mesocarp produces ethylene which stimulates cell wall degrading substances [<xref ref-type="bibr" rid="scirp.126436-ref6">6</xref>] . The fruits fall on the ground and signals the maturity of the bunch. The presence of 1 - 5 detached and/or easily detachable fruits is one of the generally accepted criteria for harvesting bunches. This phenomenon is more accentuated in the dry season than in the rainy season. In the rainy season, the bunches take longer time to reach maturity.</p></sec><sec id="s5"><title>5. Biochemical Level</title><sec id="s5_1"><title>5.1. Endocarp</title><p>The endocarp is the part of the seed that protects and allows the dispersion of the seed [<xref ref-type="bibr" rid="scirp.126436-ref11">11</xref>] . It protects the endosperm and the embryo from external shocks. In addition to protection, the endocarp plays various roles in the function of the fruit such as communication with the developing endosperm. It can be fleshy as in watermelon, fibrous as in mango, or extremely hard and durable as in a peach [<xref ref-type="bibr" rid="scirp.126436-ref11">11</xref>] . The endocarp consists mainly of lignin comparable to that of some hardwoods with lignin accounting for about 52% [<xref ref-type="bibr" rid="scirp.126436-ref12">12</xref>] .</p><sec id="s5_1_1"><title>5.1.1. Establishment of Carbohydrate Reserves</title><p>In oil palm, the accumulation of soluble sugars varies considerably during seed development [<xref ref-type="bibr" rid="scirp.126436-ref25">25</xref>] . High levels of hexoses (glucose and fructose) accumulate early in seed development. This level is due to the intense mitotic activity [<xref ref-type="bibr" rid="scirp.126436-ref26">26</xref>] . The high level of hexoses at the beginning of growth seems to be important for cell growth.</p></sec><sec id="s5_1_2"><title>5.1.2. Establishment of Mineral Reserves</title><p>Generally, mineral elements are present in high level at the beginning of seed development. Most of the minerals studied showed a high level at the beginning of seed development [<xref ref-type="bibr" rid="scirp.126436-ref10">10</xref>] . This is the case for chloride, sulphate, nitrate and potassium which decreases in the seed during its development. [<xref ref-type="bibr" rid="scirp.126436-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.126436-ref27">27</xref>] showed that there was a decrease in these mineral reserves during seed development.</p></sec><sec id="s5_1_3"><title>5.1.3. Evolution of Oil Content</title><p>During seed development, the endosperm is in a liquid form for the first 70 DAP. This organ will gradually change shape and colour during its development and will solidify as the seed approaches maturity. At the end, it is greyish-white in colour and surrounded by a fibre-covered testa strand, incorporating the embryo within it. Oil synthesis in the seed tissue takes place relatively early in the development of the seed [<xref ref-type="bibr" rid="scirp.126436-ref28">28</xref>] . It starts at about 120 DAP and continues until the fruit detaches from the bunch [<xref ref-type="bibr" rid="scirp.126436-ref28">28</xref>] , and is correlated with massive water loss [<xref ref-type="bibr" rid="scirp.126436-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.126436-ref13">13</xref>] . On the other hand, many studies have shown that the oil content in the mesocarp is correlated with the level of maturity [<xref ref-type="bibr" rid="scirp.126436-ref29">29</xref>] . Ripening of bunches is associated with a detachment of the fruits from the bunch and maximum oil content in the mesocarp [<xref ref-type="bibr" rid="scirp.126436-ref14">14</xref>] . During the fruit ripening stage, the endosperm continues to solidify probably due to lipid synthesis which lasts until 20 WAP and also to water loss [<xref ref-type="bibr" rid="scirp.126436-ref6">6</xref>] . This lipogenesis at the level of the endosperm, associated with strong dehydration and loss of potassium and calcium may contribute to increase the mass of this tissue and to solidify it [<xref ref-type="bibr" rid="scirp.126436-ref30">30</xref>] [<xref ref-type="bibr" rid="scirp.126436-ref31">31</xref>] . This development coincides with the cessation of growth of the diameter of the seed coat, and could be associated with the accumulation of lipid reserves in the mesocarp.</p></sec><sec id="s5_1_4"><title>5.1.4. Evolution of Water Content</title><p>Water plays a vital role in this part of the fruit, particularly with the growth of parenchymal cells. During the 10 first weeks after pollination, the mesocarp is continuously waterlogged [<xref ref-type="bibr" rid="scirp.126436-ref19">19</xref>] . Indeed, the water in this tissue would participate in various physiological activities, in particular the elongation and stretching of cells [<xref ref-type="bibr" rid="scirp.126436-ref18">18</xref>] , and subsequently the exponential increase in its thickness. Lipogenesis would begin between 12 and 13 Week After Pollination (WAA), followed by extensive lipogenesis associated with strong water dehydration in this tissue [<xref ref-type="bibr" rid="scirp.126436-ref19">19</xref>] . The mesocarp then becomes full of oil but with a low water content when the fruit matures.</p></sec><sec id="s5_1_5"><title>5.1.5. Development of Protein Reserves</title><p>Fruits with a hardened endocarp are usually drupes [<xref ref-type="bibr" rid="scirp.126436-ref11">11</xref>] . It protects the seed from diseases and herbivores [<xref ref-type="bibr" rid="scirp.126436-ref12">12</xref>] . The endocarp generally consists of a multi-layered sub pectin and protein arrangement [<xref ref-type="bibr" rid="scirp.126436-ref11">11</xref>] . The endocarp in the oil palm does not really have proteins, except in traces.</p></sec></sec><sec id="s5_2"><title>5.2. Mesocarp</title><sec id="s5_2_1"><title>5.2.1. Evolution of Oil Content</title><p>In the early stages of the development of this organ, the water content is very high. A timid lipogenesis starts at 84 DAP and continues until seed maturity [<xref ref-type="bibr" rid="scirp.126436-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.126436-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.126436-ref26">26</xref>] . In the immature state, the mesocarp contains a large amount of sterols. As maturity approaches these sterols decrease due to the huge amount of triglycerides synthesized [<xref ref-type="bibr" rid="scirp.126436-ref32">32</xref>] . However, one of the main resources for fruit development and lipid biosynthesis are the carbohydrates generated by biosynthesis in the leaves [<xref ref-type="bibr" rid="scirp.126436-ref26">26</xref>] . Lipid synthesis in the mesocarp occurs mainly through two distinct pathways: the first is the Kennedy pathway which relies on a sequential acylation process of fatty acids on a glycerol-3-phosphate scaffold provided by dihydroxyacetone phosphate dehydrogenase, while the second pathway relies on acyl exchange between the lipids and involves the phospholipid diacylglycerol acyltransferase. Diacylglycerol is the last intermediate before the formation of triacylglycerol in the endoplasmic reticulum. Between 18 and 20 DAP three types of fatty acids are synthesized C16:0, C18:0 and C18:1 [<xref ref-type="bibr" rid="scirp.126436-ref33">33</xref>] . Furthermore, the resulting oil yield characteristics of oil palm are an additive effect of several genes [<xref ref-type="bibr" rid="scirp.126436-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.126436-ref34">34</xref>] . For these authors, several other factors may be involved in palm oil yield: the influence of the environment and their interactions, and also the genetic origins of the palm populations.</p></sec><sec id="s5_2_2"><title>5.2.2. Evolution of Water Content</title><p>During the first 70 DAP, the mesocarp has a high and stable water content, a total absence of oil and continuous transverse growth. Between the 70th and 120th DAP, there is significant water loss and oil enrichment [<xref ref-type="bibr" rid="scirp.126436-ref9">9</xref>] . For [<xref ref-type="bibr" rid="scirp.126436-ref35">35</xref>] , high water content in early seed development is important for metabolic activity and maintenance of seed growth. At the mature stage, water loss is probably due to the deposition of storage reserves (lipids, carbohydrates, proteins) that displace water from the cells [<xref ref-type="bibr" rid="scirp.126436-ref21">21</xref>] .</p></sec><sec id="s5_2_3"><title>5.2.3. Development of Protein Reserves</title><p>Enzyme activity in developing oil palm fruit starts between 16 and 20 WAP, which corresponds to the beginning of palm oil formation in the mesocarp [<xref ref-type="bibr" rid="scirp.126436-ref25">25</xref>] . The most important enzyme in this phase is lipase. It is an important indicator of the onset of oil synthesis in the mesocarp, as its activity is linked to it. Many enzymes involved in oil biosynthesis, such as acetyl-CoA carboxylase (ACCase), acetyl-CoA: ACP transacylase, malonyl CoA: ACP transacylase, β-ketoasil-ACP synthetase, β-ketoasil-ACP reductase, β-hidroksiacyl-ACP dehydratase, enoylACP reductase, acyl-ACP thioesterase and other enzymes catalyze the formation of triacyl glycerol [<xref ref-type="bibr" rid="scirp.126436-ref21">21</xref>] . ACCase is one of those enzymes considered as key enzymes for oil biosynthesis. According to [<xref ref-type="bibr" rid="scirp.126436-ref28">28</xref>] , two proteins of the mesocarp increased considerably just before the period of the biosynthesis of oil at 12 WAP (<xref ref-type="fig" rid="fig6">Figure 6</xref>): The 34.3 kDa protein which present from 8 - 12 WAP at low concentration, but its expression then increases up to 15 WAA [<xref ref-type="bibr" rid="scirp.126436-ref28">28</xref>] . Another protein, with a 31.0 kDa MW, was also weakly expressed between 8 - 15 WAP, but more strongly at 17 WAP.</p></sec><sec id="s5_2_4"><title>5.2.4. Lipase Activity</title><p>The acidity of palm oil is correlated with the maturity level of the fruit. In mature fruits, there is a high lipase activity in the mesocarp compared to fruits at the beginning of their development. This enzyme is responsible for the massive release of free fatty acids in the mesocarp of mature fruits. Free fatty acids (FFA) are commonly used as indicators of palm oil quality [<xref ref-type="bibr" rid="scirp.126436-ref36">36</xref>] . Lipase activity is observed in the mesocarp as from 16 WAP, and shows a progressive increase until the 20th WAP. Triglyceride synthesis in the mesocarp starts from the 16th WAP</p><p>and reaches its peak at 21 weeks. Lipase activity thus appears to be correlated with lipid biosynthesis [<xref ref-type="bibr" rid="scirp.126436-ref22">22</xref>] . It is involved in the acidity of the oil produced, according to the chemical reaction below [<xref ref-type="bibr" rid="scirp.126436-ref38">38</xref>] :</p><disp-formula id="scirp.126436-formula1"><graphic  xlink:href="//html.scirp.org/file/1-2605582x11.png?20230720090135851"  xlink:type="simple"/></disp-formula></sec></sec></sec><sec id="s6"><title>6. Influence of the Environment on Bunch Maturation Parameters</title>Influence of Temperature<p>Temperature is undoubtedly a very important factor for the maturation of bunches. [<xref ref-type="bibr" rid="scirp.126436-ref39">39</xref>] , showed that high temperatures would lead to an acceleration of the vegetative cycle and result in an earlier bud break and a higher growth rate. High temperatures generally influence fruit growth rates [<xref ref-type="bibr" rid="scirp.126436-ref40">40</xref>] . Higher temperatures lead to acute shortening of the duration of the development period of the reproductive organs in many species [<xref ref-type="bibr" rid="scirp.126436-ref41">41</xref>] . For [<xref ref-type="bibr" rid="scirp.126436-ref42">42</xref>] the results are different and vary depending on the species. For maize it would be around 30˚C (<xref ref-type="fig" rid="fig7">Figure 7</xref>).</p></sec><sec id="s7"><title>7. Conclusion</title><p>In the process of bunch ripening, some main criteria are involved notably color, fruit size, water content, oil content which are the most important. They allow a better understanding of the biology of the seed, its development and the different components that make up the pericarp (endocarp, mesocarp and endosperm). Thus, it takes about 168 DAP for a bunch to mature. In addition, during the development of the seed, a series of anatomical changes are observed amongst which are the change in color and the increase in size and weight. A detailed study of these parameters has not yet been done and the present study could open up new avenues for research into innovative, faster and low-cost methods of oil palm seed production particularly before seed dormancy. Also, future research works need to be undertaken to better understand the chronological order of formation of the organic molecules of the seed reserves. This will allow us to better understand their degradation rate during the germination process, and thus possibly increase the rate of germination. This may therefore open new avenues for research to better understand the physiology of oil palm germination.</p></sec><sec id="s8"><title>Acknowledgements</title><p>The authors of this review would like to sincerely thank the UGAP (Unit&#233; de G&#233;n&#233;tique et d’Am&#233;lioration des Plantes) of the University of Yaound&#233; 1 and its supervisor for his support and guidance, Miss Lum Abienwi, all the researchers of the IRAD La Dibamba oil palm research station for their support.</p></sec><sec id="s9"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s10"><title>Cite this paper</title><p>Eya’a, N.C., Nsimi, M.A., Ndele, P.H., Ngalle, B.H., Molo, T., Mbo, N.L.F., Fouman, A., Likeng, L.-G.B., Ngando, E.G.F. and Bell, J.M. (2023) A Review of Main Factors Involved in the Maturation of Oil Palm (Elaeis guineensis Jacq.) Fruit Bunches. American Journal of Plant Sciences, 14, 727-740. https://doi.org/10.4236/ajps.2023.147049</p></sec></body><back><ref-list><title>References</title><ref id="scirp.126436-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">https://ipad.fas.usda.gov/cropexplorer/cropview/commodityView.aspx?cropid=4243000</mixed-citation></ref><ref id="scirp.126436-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Hoyle, D. and Levang, P. (2012) Le développement du palmier à huile au Cameroun. WWF, Yaoundé, 23 p.</mixed-citation></ref><ref id="scirp.126436-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Harun, M.H. and Noor, M.R.M. (2002) Fruit Set and Oil Palm Bunch Components. Journal of Oil Palm Research, 14, 24-33.</mixed-citation></ref><ref id="scirp.126436-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Corley, R. (1976) Sex Differentiation in Oil Palm: Effects of Growth Regulators. Journal of Experimental Botany, 27, 553-558. https://doi.org/10.1093/jxb/27.3.553</mixed-citation></ref><ref id="scirp.126436-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Wong, Y. and Hardon, J. (1971) A Comparison of Different Methods of Assisted Pollination in the Oil Palm. Chemara Research Station, Seremban.</mixed-citation></ref><ref id="scirp.126436-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Corley, R. and Tinker, P. (2015) The Oil Palm. Fifth Edition, John Wiley and Sons, Oxford, 239. https://doi.org/10.1002/9781118953297</mixed-citation></ref><ref id="scirp.126436-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Forster, B.P., Rusfiandi, H., Sitorus, A., et al. (2011) Oil Palm Fruit Development. PIPOC 2011 International Palm Oil Congress: Palm Oil Fortifying the World, Kuala Lumpur, 15-17 November 2011, 161-166.</mixed-citation></ref><ref id="scirp.126436-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Judd, W.S., Campbell, C.S., Kellogg, E.A. and Stevens, P. (2002) Botanique systématique: Une perspective phylogénétique. De Boeck Supérieur, Paris, 488 p.</mixed-citation></ref><ref id="scirp.126436-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Ngalle, H.B., Bell, J.M., Ngando-Ebongue, G.F., Eman-Evina, H., Ntsomboh, G.N. and Nsimi-Mva, A. (2014) Morphogenesis of Oil Palm (Elaeis guineensis Jacq.) Fruit in Seed Development. Journal of Life Sciences, 8, 946-954.</mixed-citation></ref><ref id="scirp.126436-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Kok, S.-Y., Namasivayam, P., Ee, G.C.-L. and Ong-Abdullah, M. (2013) Biochemical Characterisation during Seed Development of Oil Palm (Elaeis guineensis). Journal of Plant Research, 126, 539-547. https://doi.org/10.1007/s10265-013-0560-8</mixed-citation></ref><ref id="scirp.126436-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Crombie, W.M. (1956) Fat Metabolism in the West African Oil Palm (Elaeis guineensis) Part I. Fatty Acid Formation in the Maturing Kernel. Journal of Experimental Botany, 7, 181-193. https://doi.org/10.1093/jxb/7.2.181</mixed-citation></ref><ref id="scirp.126436-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Oo, K.-C., The, S.-K., Khor, H.-T. and Ong, A.S. (1985) Fatty Acid Synthesis in the Oil Palm (Elaeis guineensis): Incorporation of Acetate by Tissue Slices of the Developing Fruit. Lipids, 20, 205-210. https://doi.org/10.1007/BF02534189</mixed-citation></ref><ref id="scirp.126436-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Saka, S., Munusamy, M., Shibata, M., Tono, Y. and Miyafuji, H. (2008) Chemical Constituents of the Different Anatomical Parts of the Oil Palm (Elaeis guineensis) for Their Sustainable Utilization. Seminar Proceedings—Natural Resources &amp; Energy Environment JSPS-VCC Program on Environmental Science, Engineering and Ethics (Group IX), Kyoto, 24-25 November 2008, 19-34.</mixed-citation></ref><ref id="scirp.126436-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Thomas, R., Sew, P., Mok, C., Chan, K., Easau, P. and Ng, S. (1971) Fruit Ripening in the Oil-Palm Elaeis guineensis. Annals of Botany, 35, 1219-1225.  
https://doi.org/10.1093/oxfordjournals.aob.a084556</mixed-citation></ref><ref id="scirp.126436-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Henry, P. (1952) La germination des graines d’Elaeis (Suite et fin). Revue Internationale de Botanique Appliquée et d’agriculture Tropicale, 32, 66-77.  
https://doi.org/10.3406/jatba.1952.6773</mixed-citation></ref><ref id="scirp.126436-ref16"><label>16</label><mixed-citation publication-type="other" xlink:type="simple">Vallade, J. (1965) Recherches morphologique et cytologique sur l’embryon d’Elaeis guineensis Jacq. Quiescent et en cours de germination, Dijon, 18 p.</mixed-citation></ref><ref id="scirp.126436-ref17"><label>17</label><mixed-citation publication-type="other" xlink:type="simple">Opute, F. (1975) Lipid Composition and the Role of the Haustorium in the Young Seedling of the West African Oil Palm, Elaeis guineensis Jacq. Annals of Botany, 39, 1057-1061. https://doi.org/10.1093/oxfordjournals.aob.a085024</mixed-citation></ref><ref id="scirp.126436-ref18"><label>18</label><mixed-citation publication-type="other" xlink:type="simple">Hussey, G. (1958) An Analysis of the Factors Controlling the Germination of the Seed of the Oil Palm, Elaeis guineensis (Jacq.). Annals of Botany, 22, 259-284.  
https://doi.org/10.1093/oxfordjournals.aob.a083610</mixed-citation></ref><ref id="scirp.126436-ref19"><label>19</label><mixed-citation publication-type="other" xlink:type="simple">Prevot, P. (1962) Physiologie des plantes tropicales cultivées. ORSTOM, Paris, 39 p.</mixed-citation></ref><ref id="scirp.126436-ref20"><label>20</label><mixed-citation publication-type="other" xlink:type="simple">Ngalle, H.B., Bell, J.M., Ebongue, G.F.N., Nyobe, L., Ngangnou, F.C. and Ntsomboh, G.N. (2013) Morphogenesis of Oil Palm Fruit (Elaeis guineensis Jacq.) in Mesocarp and Endocarp Development. Journal of Life Sciences, 7, 153-158.  
https://doi.org/10.17265/1934-7391/2013.02.008</mixed-citation></ref><ref id="scirp.126436-ref21"><label>21</label><mixed-citation publication-type="book" xlink:type="simple">Sambanthamurthi, R., Cheang, O.K. and Parman, S.H. (1995) Factors Affecting Lipase Activity in the Oil Palm (Elaeis guineensis) Mesocarp. In: Kader, J.-C. and Mazliak, P., Eds., Plant Lipid Metabolism, Springer, New York, 555-557.  
https://doi.org/10.1007/978-94-015-8394-7_155</mixed-citation></ref><ref id="scirp.126436-ref22"><label>22</label><mixed-citation publication-type="other" xlink:type="simple">Heller, R., Esnault, R. and Lance, C. (2004) Physiologievégétale: Développement. Dunod, Paris, 366 p.</mixed-citation></ref><ref id="scirp.126436-ref23"><label>23</label><mixed-citation publication-type="other" xlink:type="simple">Heller, R., Esnault, R. and Lance, C. (2004) Physiologievégétale. N II développement. 6th éditions, Dunod, Paris, 323 p.</mixed-citation></ref><ref id="scirp.126436-ref24"><label>24</label><mixed-citation publication-type="other" xlink:type="simple">Mensah, G. (1999) Le palmier à huile, unarbre à buts multiples et une source de technologies traditionnelles variées. Bulletin de la Recherche Agronomique du Bénin, 9 p.</mixed-citation></ref><ref id="scirp.126436-ref25"><label>25</label><mixed-citation publication-type="other" xlink:type="simple">Lehninger, A., Nelson, D. and Cox, M. (1993) Principles of Biochemistry. 2nd Edition, Worth Publishers, New York.</mixed-citation></ref><ref id="scirp.126436-ref26"><label>26</label><mixed-citation publication-type="other" xlink:type="simple">Weber, M., Davies, J.J., Wittig, D., Oakeley, E.J., Haase, M., Lam, W.L. and Schuebeler, D. (2005) Chromosome-Wide and Promoter-Specific Analyses Identify Sites of Differential DNA Methylation in Normal and Transformed Human Cells. Nature Genetics, 37, 853-862. https://doi.org/10.1038/ng1598</mixed-citation></ref><ref id="scirp.126436-ref27"><label>27</label><mixed-citation publication-type="other" xlink:type="simple">Dardick, C. and Callahan, A.M. (2014) Evolution of the Fruit Endocarp: Molecular Mechanisms Underlying Adaptations in Seed Protection and Dispersal Strategies. Frontiers in Plant Science, 5, Article No. 284.  
https://doi.org/10.3389/fpls.2014.00284</mixed-citation></ref><ref id="scirp.126436-ref28"><label>28</label><mixed-citation publication-type="other" xlink:type="simple">Chevalier, A. (1925) La Maturation des Fruits du Palmier à huile. Journal d’agriculture Traditionnelle et de Botanique Appliquée, 5, 122-131.  
https://doi.org/10.3406/jatba.1925.4263</mixed-citation></ref><ref id="scirp.126436-ref29"><label>29</label><mixed-citation publication-type="other" xlink:type="simple">Wuidart, W. (1973) Evolution de la lipogenèse du régime de palmier à huileenfonction du pourcentage de fruits detaches. La Mé, 551 p.</mixed-citation></ref><ref id="scirp.126436-ref30"><label>30</label><mixed-citation publication-type="other" xlink:type="simple">Pérez, H.E., Hill, L.M. and Walters, C. (2012) An Analysis of Embryo Development in Palm: Interactions between Dry Matter Accumulation and Water Relations in Pritchardia remota (Arecaceae). Seed Science Research, 22, 97-111.  
https://doi.org/10.1017/S0960258511000523</mixed-citation></ref><ref id="scirp.126436-ref31"><label>31</label><mixed-citation publication-type="other" xlink:type="simple">Aberlenc-Bertossi, F., Chabrillange, N., Corbineau, F. and Duval, Y. (2003) Acquisition of Desiccation Tolerance in Developing Oil Palm (Elaeis guineensis Jacq.) Embryos in Planta and in Vitro in Relation to Sugar Content. Seed Science Research, 13, 179-186. https://doi.org/10.1079/SSR2003135</mixed-citation></ref><ref id="scirp.126436-ref32"><label>32</label><mixed-citation publication-type="other" xlink:type="simple">Akinola, F., Oguntibeju, O., Adisa, A., Owojuyigbe, O., et al. (2010) Physico-Chemical Properties of Palm Oil from Different Palm Oil Local Factories in Nigeria. Journal of Food, Agriculture &amp; Environment, 8, 264-269.</mixed-citation></ref><ref id="scirp.126436-ref33"><label>33</label><mixed-citation publication-type="other" xlink:type="simple">The, H.F., Neoh, B.K., Hong, M.P.L., Low, J.Y.S. and Ng, T.L.M. (2013) Differential Metabolite Profiles during Fruit Development in High-Yielding Oil Palm Mesocarp. PLOS ONE, 8, 61344. https://doi.org/10.1371/journal.pone.0061344</mixed-citation></ref><ref id="scirp.126436-ref34"><label>34</label><mixed-citation publication-type="other" xlink:type="simple">Wong, Y.C., The, H.F., Mebus, K., Ooi, T.E.K. and Kwong, Q.B. (2017) Differential Gene Expression at Different Stages of Mesocarp Development in High- and Low-Yielding Oil Palm. BMC Genomics, 18, Article No. 470.  
https://doi.org/10.1186/s12864-017-3855-7</mixed-citation></ref><ref id="scirp.126436-ref35"><label>35</label><mixed-citation publication-type="other" xlink:type="simple">Westgate, M.E. and Grant, D.L.T. (1989) Water Deficits and Reproduction in Maize: Response of the Reproductive Tissue to Water Deficits at Anthesis and Mid-Grain Fill. Plant Physiology, 91, 862-867. https://doi.org/10.1104/pp.91.3.862</mixed-citation></ref><ref id="scirp.126436-ref36"><label>36</label><mixed-citation publication-type="other" xlink:type="simple">Nizam, A.A., Muthiyah, K. and Mahmud, M. (2020) Free Fatty Acid Formation in Oil Palm Fruits during Storage. IOP Conference Series: Materials Science and Engineering, 991, Article ID: 012009. https://doi.org/10.1088/1757-899X/991/1/012009</mixed-citation></ref><ref id="scirp.126436-ref37"><label>37</label><mixed-citation publication-type="other" xlink:type="simple">Kermode, A.R. (1990) Regulatory Mechanisms Involved in the Transition from Seed Development to Germination. Critical Reviews in Plant Sciences, 9, 155-195.  
https://doi.org/10.1080/07352689009382286</mixed-citation></ref><ref id="scirp.126436-ref38"><label>38</label><mixed-citation publication-type="other" xlink:type="simple">Patil, K.J., Chopda, M.Z. and Mahajan, R.T. (2011) Lipase Biodiversity. Indian Journal of Science and Technology, 4, 971-982.  
https://doi.org/10.17485/ijst/2011/v4i8.30</mixed-citation></ref><ref id="scirp.126436-ref39"><label>39</label><mixed-citation publication-type="other" xlink:type="simple">Ammar, A. (2014) Etude des Effets de fortes températures sur la production du pêcher et la qualité des fruits. PhD Thesis, Institut National d’Etudes Supérieures Agronomiques de Montpellier, Montpellier, 13 p.</mixed-citation></ref><ref id="scirp.126436-ref40"><label>40</label><mixed-citation publication-type="other" xlink:type="simple">Okello, R.C., de Visser, P.H., Heuvelink, E., Lammers, M., de Maagd, R.A., Struik, P.C. and Marcelis, L.F. (2015) A Multilevel Analysis of Fruit Growth of Two Tomato Cultivars in Response to Fruit Temperature. Physiologia Plantarum, 153, 403-418.  
https://doi.org/10.1111/ppl.12247</mixed-citation></ref><ref id="scirp.126436-ref41"><label>41</label><mixed-citation publication-type="other" xlink:type="simple">Adra, F. (2017) Etude des effets d’une élévation de température sur la croissanceet le développement du pêcher: Conséquences sur la qualité des fruits. PhD Thesis, Universitéd’ Avignon, Avignon, 13 p.</mixed-citation></ref><ref id="scirp.126436-ref42"><label>42</label><mixed-citation publication-type="other" xlink:type="simple">Hatfield, J.L. and Prueger, J.H. (2015) Temperature Extremes: Effect on Plant Growth and Development. Weather and Climate Extremes, 10, 4-10.  
https://doi.org/10.1016/j.wace.2015.08.001</mixed-citation></ref></ref-list></back></article>